Document Details

Generated Narrative: Bundle TEST PURPOSES ONLY - vizimpro

Document Subject

Generated Narrative: MedicinalProductDefinition mp99b35aa72c0e418c8749ea99edf139d2

identifier: http://ema.europa.eu/identifier/EU/1/19/1354/001

type: Medicinal Product

domain: Human use

status: active

legalStatusOfSupply: Medicinal product subject to medical prescription

name

productName: Vizimpro 15 mg film-coated tablets

type: Full name

part

part: nan

type: Invented name part

part

part: nan

type: Scientific name part

part

part: nan

type: Strength part

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part: nan

type: Pharmaceutical dose form part

Usages

-	Country	Jurisdiction	Language
*	EU	EU	en

Document Content

Generated Narrative: Composition composition-en-99b35aa72c0e418c8749ea99edf139d2

identifier: http://ema.europa.eu/identifier/EU/1/19/1354/001

status: Final

type: Package Leaflet

category: Raw

date: 2022-02-16 13:28:17+0000

author: Organization ACME industry

title: TEST PURPOSES ONLY - vizimpro

Attesters

What is in this leaflet

1. What Vizimpro is and what it is used for
2. What you need to know before you take Vizimpro
3. How to take Vizimpro
4. Possible side effects
5. How to store Vizimpro
6. Contents of the pack and other information

Vizimpro contains the active substance dacomitinib, which belongs to a group of medicines called protein tyrosine kinase inhibitors which are used to treat cancer.

Vizimpro is used to treat adults with a type of lung cancer called non-small cell lung cancer . If a test has shown that your cancer has certain changes (mutations) in a gene called EGFR (epidermal growth factor receptor) and has spread to your other lung or other organs, your cancer is likely to respond to treatment with Vizimpro.

Vizimpro can be used as your first treatment once your lung cancer has spread to your other lung or other organs.

Do not take Vizimpro

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

Warnings and precautions
Talk to your doctor, pharmacist or nurse before taking Vizimpro:

• if you ever had any other lung problems. Some lung problems may get worse during treatment with Vizimpro, as Vizimpro may cause inflammation of the lungs during treatment. Symptoms may be similar to those from lung cancer. Tell your doctor right away if you have any new or worsening symptoms including difficulty in breathing, shortness of breath, or cough with or without phlegm (mucous), or fever.
• If you are being treated with any of the medicines listed in section Other medicines and Vizimpro.

Tell your doctor immediately while taking this medicine:

• if you develop diarrhoea. Immediate treatment of diarrhoea is important.
• if you develop skin rash. Early treatment of skin rash is important.
• if you have any symptoms of a liver problem which may include: yellowing of your skin or the white part of your eyes (jaundice), dark or brown (tea coloured) urine, light-coloured bowel movements (stools).

Children and adolescents Vizimpro has not been studied in children or adolescents and it must not be given to patients under the age of 18 years.

Other medicines and Vizimpro Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.

In particular, the effects of some medicines may increase when taken with Vizimpro. These include, among others:

• Procainamide, used to treat heart arrhythmias
• Pimozide and thioridazine, used to treat schizophrenia and psychosis

You should not take these medicines during your treatment with Vizimpro.

The following medicines may reduce how well Vizimpro works:

• Long-acting medicines for reducing stomach acid, such as proton pump inhibitors (for ulcers, indigestion and heartburn).

You should not take these medicines during your treatment with Vizimpro. As an alternative, you can take a short-acting medicine, such as an antacid, or an H2 blocker medicine. If you take H2 blocker medicine take your dose of Vizimpro at least 2 hours before or 10 hours after taking the H2 blocker medicine.

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

Pregnancy You should not become pregnant during treatment with Vizimpro because this medicine could harm the baby. If there is any possibility that you may become pregnant you must use effective contraception during treatment, and for at least 17 days afterwards. If you become pregnant while taking this medicine, you should immediately talk to your doctor.

Breast-feeding Do not breast-feed while taking this medicine because it is not known if it can harm your baby.

Driving and using machines Tiredness and eye irritation can occur in patients taking Vizimpro. If you feel tired or your eyes are irritated, you should use caution when driving or using machines.

Vizimpro contains lactose and sodium This medicine contains lactose (found in milk or dairy products). If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicine.

This medicine contains less than 1 mmol sodium (23 mg) per tablet, that is to say essentially sodium-free .

Always take this medicine exactly as your doctor or pharmacist has told you. Check with your doctor or pharmacist if you are not sure.

• The recommended dose is 45 mg taken by mouth each day.
• Take the tablet at about the same time each day.
• Swallow the tablet whole with a glass of water.
• You can take the tablet with or without meals.

Your doctor may decrease the dose of your medicine depending on how well you tolerate it.

If you take more Vizimpro than you should If you have taken too much Vizimpro, see a doctor or go to a hospital immediately.

If you forget to take Vizimpro If you miss a dose or vomit, take your next dose as scheduled. Do not take a double dose to make up for a forgotten tablet.

If you stop taking Vizimpro Do not stop taking Vizimpro unless your doctor tells you to. If you have any further questions on 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.

Contact your doctor immediately if you notice any of the following side effects you may need urgent medical treatment: Inflammation of the lungs (common, may affect up to 1 in 10 people) Difficulty in breathing, shortness of breath, possibly with a cough or fever. This may mean that you have an inflammation of the lungs called interstitial lung disease and can be fatal.
Diarrhoea (very common, may affect more than 1 in 10 people)
Diarrhoea may lead to fluid loss (common), low blood potassium (very common), and worsening kidney function and can be fatal. At first signs of increased frequency of bowel movements, contact your doctor immediately, drink plenty of fluids, and start antidiarrhoea treatment as soon as possible. You should have an anti-diarrhoeal medicine available before you start taking Vizimpro. Skin rash (very common) It is important to treat the rash early. Tell your doctor if a rash starts. If treatment for rash is not working or the rash is getting worse (for example, you have peeling or cracking of the skin) you should tell your doctor immediately, since your doctor may decide to stop your treatment with Vizimpro. Rash may occur or worsen in areas exposed to sun. Sun protection with protective clothing and sunscreen is recommended.

Tell your doctor as soon as possible if you notice any of the other following side effects:

Very common (may affect more than 1 in 10 people): Inflammation of the mouth and lips Nail problems Dry skin Loss of appetite Dry, red, or itchy eyes Weight loss Hair loss Itching Abnormal liver enzyme blood tests Nausea or vomiting Flushed or painful palms or soles Tiredness Weakness Cracks in the skin

Common (may affect up to 1 in 10 people): Alteration in taste Peeling skin Eyes inflammation Abnormal amount of body hair growth

Reporting of side effects If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects 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 and the blister after EXP. The expiry date refers to the last day of that month.

This medicine does not require any special storage conditions.

This medicine may pose a risk for the environment. Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.

What Vizimpro contains

• The active substance is dacomitinib (as dacomitinib monohydrate). Vizimpro film-coated tablets come in different strengths. Vizimpro 15 mg tablet: each film-coated tablet contains 15 mg dacomitinib Vizimpro 30 mg tablet: each film-coated tablet contains 30 mg dacomitinib Vizimpro 45 mg tablet: each film-coated tablet contains 45 mg dacomitinib
• The other ingredients are:
  Tablet core: lactose monohydrate, microcrystalline cellulose, sodium starch glycolate, magnesium stearate (see section 2 Vizimpro contains lactose and sodium). Film coating: Opadry II Blue 85F30716 containing polyvinyl alcohol partially hydrolysed (E1203), talc (E553b), titanium dioxide (E171), macrogol (E1521), Indigo carmine aluminium lake (E132).

What Vizimpro looks like and contents of the pack

• Vizimpro 15 mg film-coated tablets are supplied as blue film-coated, round biconvex tablets, debossed with Pfizer on one side and DCB15 on the other.

• Vizimpro 30 mg film-coated tablets are supplied as blue film-coated, round biconvex tablet, debossed with Pfizer on one side and DCB30 on the other.

• Vizimpro 45 mg film-coated tablets are supplied as blue film-coated, round biconvex tablet, debossed with Pfizer on one side and DCB45 on the other.

It is available in blister packs of 30 film-coated tablets (tablets).

Marketing Authorisation Holder Pfizer Europe MA EEIG Boulevard de la Plaine 1050 Bruxelles Belgium

Manufacturer Pfizer Manufacturing Deutschland GmbH Betriebsst tte Freiburg Mooswaldallee 1 79090 Freiburg Germany

For any information about this medicine, please contact the local representative of the Marketing Authorisation Holder:

Belgi /Belgique/Belgien Luxembourg/Luxemburg Pfizer NV/SA T l/Tel: +32 (0)2 554 62 Lietuva Pfizer Luxembourg SARL filialas Lietuvoje Tel. + 370 52 51 4
,
.: +359 2 970 4Magyarorsz g Pfizer Kft. Tel.: +36-1-488-37- esk republika Pfizer, spol. s r.o. Tel.: +420 283 004 Malta Vivian Corporation Ltd. Tel: + 35621 344Danmark Pfizer ApS Tlf: +45 44 20 11 Nederland Pfizer BV Tel: +31 (0)10 406 43 Deutschland PFIZER PHARMA GmbH Tel: +49 (0)30 550055-51Norge Pfizer AS Tlf: +47 67 52 61 Eesti Pfizer Luxembourg SARL Eesti filiaal
Tel.: +372 666 7 sterreich Pfizer Corporation Austria Ges.m.b.H. Tel: +43 (0)1 521 15-0

Pfizer A.E. .: +30 210 6785 Polska Pfizer Polska Sp. z o.o. Tel.:+48 22 335 61 Espa a Pfizer, S.L. Tel: +34 91 490 99 Portugal Laborat rios Pfizer, Lda. Tel: +351 21 423 5France Pfizer
T l: +33 (0)1 58 07 34 Rom nia Pfizer Romania S.R.L. Tel: +40 (0) 21 207 28 Hrvatska Pfizer Croatia d.o.o. Tel: +385 1 3908 Slovenija Pfizer Luxembourg SARL Pfizer, podru nica za svetovanje s podro ja farmacevtske dejavnosti, Ljubljana Tel.: + 386 (0)1 52 11 Ireland Pfizer Healthcare Ireland Tel: 1800 633 363 (toll free) +44 (0)1304 616Slovensk republika Pfizer Luxembourg SARL, organiza n zlo ka
Tel.: + 421 2 3355 5 sland Icepharma hf. S mi: +354 540 8Suomi/Finland Pfizer Oy Puh./Tel: +358 (0)9 43 00 Italia Pfizer S.r.l. Tel: +39 06 33 18 Sverige
Pfizer AB Tel: +46 (0)8 550 520 K
Pfizer . . (Cyprus Branch)
: +357 22 817United Kingdom (Northern Ireland) Pfizer Limited Tel: +44 (0) 1304 616Latvija Pfizer Luxembourg SARL fili le Latvij
Tel.: + 371 670 35 This leaflet was last revised in MM/YYYY

Detailed information on this medicine is available on the European Medicines Agency web site: