ERLOTINIB SUN 25 MG FILM-COATED TABLETS - patient leaflet, side effects, dosage

Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.

• – Keep this leaflet. You may need to read it again.

• – If you have further questions, ask your doctor or pharmacist.

• – This medicine has been prescribed for you only. Do not pass it on to others. It may harm

them, even if their signs of illness are the same as yours.

• – If you get any side effects, talk to your doctor or pharmacist. This includes any possible side

effects not listed in this leaflet. See section 4.

What is in this leaflet

• 1. What Erlotinib SUN is and what it is used for

• 2. What you need to know before you take Erlotinib SUN

• 3. How to take Erlotinib SUN

• 4. Possible side effects

• 5. How to store Erlotinib SUN

• 6. Contents of the pack and other information

1. what erlotinib sun is and what it is used for

Erlotinib SUN contains the active substance erlotinib. Erlotinib SUN is a medicine used to treat cancer by preventing the activity of a protein called epidermal growth factor receptor (EGFR). This protein is known to be involved in the growth and spread of cancer cells.

Erlotinib SUN is indicated for adults. This medicine can be prescribed to you if you have non-small cell lung cancer at an advanced stage. It can be prescribed as initial therapy or as therapy if your disease remains largely unchanged after initial chemotherapy, provided your cancer cells have specific EGFR mutations. It can also be prescribed if previous chemotherapy has not helped to stop your disease.

This medicine can also be prescribed to you in combination with another treatment called gemcitabine if you have cancer of the pancreas at a metastatic stage.

2. what you need to know before you take erlotinib sun- if you are allergic to erlotinib or any of the ingredients of this medicine (listed in section 6).

Warnings and precautions:

Talk to your doctor before using Erlotinib SUN:

• – if you are taking other medicines that may increase or decrease the amount of erlotinib SUN

in your blood or influence its effect (for example antifungals like ketoconazole, protease inhibitors, erythromycin, clarithromycin, phenytoin, carbamazepine, barbiturates, rifampicin, ciprofloxacin, omeprazole, ranitidine, St. John’s Wort or proteasome inhibitors). In some cases these medicines may reduce the efficacy or increase the side effects of Erlotinib SUN, and your doctor may need to adjust your treatment. Your doctor might avoid treating you with these medicines while you are receiving Erlotinib SUN.

• – if you are taking anticoagulants (a medicine which helps to prevent thrombosis or blood

clotting e.g. warfarin), Erlotinib SUN may increase your tendency to bleed. Talk to your doctor, he will need to regularly monitor you with some blood tests.

• – if you are taking statins (medicines to lower your blood cholesterol), Erlotinib SUN may

increase the risk of statin related muscle problems, which on rare occasions can lead to serious muscle breakdown (rhabdomyolysis) resulting in kidney damage.

• – if you use contact lenses and/or have a history of eye problems such as severe dry eyes,

inflammation of the front part of the eye (cornea) or ulcers involving the front part of the eye.

See also below “Other medicines and Erlotinib SUN”.

You should also tell your doctor:

• – if you have sudden difficulty in breathing associated with cough or fever because your doctor

may need to treat you with other medicines and interrupt your Erlotinib SUN treatment;

• – if you have diarrhoea because your doctor may need to treat you with anti-diarrhoeal (for

example loperamide);

• – immediately, if you have severe or persistent diarrhoea, nausea, loss of appetite, or vomiting

because your doctor may need to interrupt your Erlotinib SUN treatment and may need to treat you in the hospital;

• – if you have severe pain in the abdomen, severe blistering or peeling of skin. Your doctor may

need to interrupt or stop your treatment;

• – if you develop acute or worsening redness and pain in the eye, increased eye watering, blurred

vision and/or sensitivity to light, please tell your doctor or nurse immediately as you may need urgent treatment (see Possible Side Effects below).

• – if you are also taking a statin and experience unexplained muscle pain, tenderness, weakness

or cramps. Your doctor may need to interrupt or stop your treatment.

See also section 4 “Possible side effects”.

Liver or kidney disease

It is not known whether Erlotinib SUN has a different effect if your liver or kidneys are not functioning normally. The treatment with this medicine is not recommended if you have a severe liver disease or severe kidney disease.

Glucuronidation disorder, like Gilbert’s syndrome

Your doctor must treat you with caution if you have a glucuronidation disorder like Gilbert’s syndrome.

Smoking

You are advised to stop smoking if you are treated with Erlotinib SUN as smoking could decrease the amount of your medicine in the blood.

Children and adolescents

Erlotinib SUN has not been studied in patients under the age of 18 years. The treatment with this medicine is not recommended for children and adolescents.

Other medicines and Erlotinib SUN

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

Erlotinib SUN with food and drink

Do not take Erlotinib SUN with food. See also section 3 ‘How to take Erlotinib SUN’

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

Avoid pregnancy while being treated with Erlotinib SUN. If you could become pregnant, use adequate contraception during treatment, and for at least 2 weeks after taking the last tablet. If you become pregnant while you are being treated with Erlotinib SUN, immediately inform your doctor who will decide if the treatment should be continued.

Breast-feeding

Do not breast-feed if you are being treated with Erlotinib SUN, and for at least 2 weeks after taking the last tablet.

Driving and using machines

Erlotinib SUN has not been studied for its possible effects on the ability to drive and use machines but it is very unlikely that your treatment will affect this ability.

Erlotinib SUN contains a sugar called lactose monohydrate.

If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking Erlotinib SUN.

3. how to take erlotinib sun

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

Erlotinib SUN is for oral use.

The tablet should be taken at least one hour before or two hours after the ingestion of food.

The usual dose is one tablet of Erlotinib SUN 150 mg each day if you have non-small cell lung cancer.

The usual dose is one tablet of Erlotinib SUN 100 mg each day if you have metastatic pancreatic cancer.

Erlotinib SUN is given in combination with gemcitabine treatment.

Your doctor may adjust your dose in 50 mg steps. For the different dose regimens, Erlotinib SUN is available in strengths of 25 mg, 100 mg or 150 mg.

If you take more Erlotinib SUN than you should

Contact your doctor or pharmacist immediately.

You may have increased side effects and your doctor may interrupt your treatment.

If you forget to take Erlotinib SUN

If you miss one or more doses of Erlotinib SUN, contact your doctor or pharmacist as soon as possible.

Do not take a double dose to make up for a forgotten dose.

If you stop taking Erlotinib SUN

It is important to keep taking Erlotinib SUN every day, as long as your doctor prescribes it for you.

If you have any further questions on the use of this medicine, ask your doctor or pharmacist.

4. possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them.

Contact your doctor as soon as possible if you suffer from any of the below side effects. In some cases your doctor may need to reduce your dose of Erlotinib SUN or interrupt treatment:

• – Diarrhoea and vomiting (very common: may affect more than 1 out of 10 people).

Persistent and severe diarrhoea may lead to low blood potassium and impairment of your kidney function, particularly if you receive other chemotherapy treatments at the same time. If you experience more severe or persistent diarrhoea contact your doctor immediately as your doctor may need to treat you in the hospital.

• – Eye irritation due to conjunctivitis/ke­ratoconjuncti­vitis (very common: may affect more

than 1 out of 10 people) and keratitis (common: may affect up to 1 in 10 people).

• – A particular form of lung irritation called interstitial lung disease (uncommon in European

patients; common in Japanese patients: may affect up to 1 in 100 people in Europe and up to 1 in10 in Japan). This disease can also be linked to the natural progression of your medical condition and can have a fatal outcome in some cases. If you develop symptoms such as sudden difficulty in breathing associated with cough or fever contact your doctor immediately as you could suffer from this disease. Your doctor may decide to permanently stop your treatment with Erlotinib SUN.

• – Gastrointestinal perforations have been observed (uncommon: may affect up to 1 in 100

people). Tell your doctor if you have severe pain in your abdomen. Also, tell your doctor if you had peptic ulcers or diverticular disease in the past, as this may increase this risk.

• – In rare cases liver failure was observed (rare: may affect up to 1 in 1,000 people). If your

blood tests indicate severe changes in your liver function, your doctor may need to interrupt your treatment.

Very common side effects (may affect more than 1 in 10 people):

• – Rash which may occur or worsen in sun exposed areas. If you are exposed to sun,

protective clothing, and/or use of sun screen (e.g. mineral-containing) may be advisable

• – Infection

• – Loss of appetite, decreased weight

• – Depression

• – Headache, altered skin sensation or numbness in the extremities

• – Difficulty in breathing, cough

• – Nausea

• – Mouth irritation

• – Stomach pain, indigestion and flatulence

• – Abnormal blood tests for the liver function

• – Itching, dry skin and loss of hair

• – Tiredness, fever, rigors

Common side effects (may affect up to 1 in 10 people):

• – Bleeding from the nose

• – Bleeding from the stomach or the intestines

• – Inflammatory reactions around the fingernail

• – Infection of hair follicles

• – Acne

• – Cracked skin (skin fissures)

• – Reduced kidney function (when given outside the approved indications in combination with

chemotherapy)

Uncommon side effects (may affect up to 1 in 100 people):

• – Eyelash changes

• – Excess body and facial hair of a male distribution pattern

• – Eyebrow changes

• – Brittle and loose nails

Rare side effects (may affect up to 1 in 1,000 people):

• – Flushed or painful palms or soles (Palmar plantar erythrodysaesthesia syndrome)

Very rare side effects (may affect up to 1 in 10,000 people):

• – Cases of perforation or ulceration of the cornea

• – Severe blistering or peeling of skin (suggestive of Stevens-Johnson syndrome)

• – Inflammation of the coloured part of the eye

Reporting of side effects

If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme at: or search for MHRA Yellow Card in the Google Play or Apple App Store. By reporting side effects you can help provide more information on the safety of this medicine.

5. how to store erlotinib sun

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 refers to the last day of that month.

This medicine does not require any special storage conditions.

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 to protect the environment.

6. contents of the pack and other information- the active substance of erlotinib sun is erlotinib. each film-coated tablet contains erlotinib

25 mg, 100 mg or 150 mg (as erlotinib hydrochloride), depending on the strength.

• - The other ingredients are: Tablet core: lactose monohydrate, microcrystalline cellulose

What Erlotinib SUN looks like and contents of the pack:

Erlotinib SUN 25 mg tablets are white to off white round biconvex film coated tablets, 6.18 mm in diameter, debossed with „RL“ on one side and „11“ on other side.

Erlotinib SUN 100 mg tablets are white to off white round biconvex film coated tablets, 9.63 mm in diameter, debossed with „RL“ on one side and „12“ on other side.

Erlotinib SUN 150 mg tablets are white to off white round biconvex film coated tablets, 11.2 mm in diameter, debossed with „RL“ on one side and „13“ on other side.

Pack sizes:

Blister packs

30 film-coated tablets supplied in OPA/Al/HDPE/P­E+Desiccant/HDPE/PE/Al blisters (3 × 10 film-coated tablets).

HDPE bottles

30 film-coated tablets supplied in HDPE bottles with child-resistant cap and induction seal liner, containing silica gel.

Marketing Authorisation Holder

Sun Pharmaceutical Industries Europe B.V.

Polarisavenue 87

2132JH Hoofddorp

The Netherlands

Manufacturers

Sun Pharmaceutical Industries Europe B.V.

Polarisavenue 87

2132JH Hoofddorp

The Netherlands

Terapia S.A.

Str. Fabricii nr.124,

400632, Cluj-Napoca,

Romania

This medicinal product is authorised in the Member States of the EEA under the following names:

This leaflet was last revised in October 2019