Kexrolt: detailed information

PACKAGE LEAFLET

Package leaflet: information for the user

KEXROLT 10 mg/10 mg film-coated tablets, 10 mg/20 mg film-coated tablets, 10 mg/40 mg film-coated tablets, 10 mg/80 mg film-coated tablets

ezetimibe and atorvastatin
Please read this leaflet carefully before taking this medicine because it contains important information for you.

Keep this leaflet. You may need to read it again.
If you have any questions, ask your doctor or pharmacist.
This medicine has been prescribed for you only. Do not give it to others, even if their symptoms are the same as yours, as it could be harmful.
If you experience any side effects, including those not listed in this leaflet, inform your doctor or pharmacist. See section 4.

Contents of this leaflet:

What KEXROLT is and what it is used for
What you need to know before taking KEXROLT
How to take KEXROLT
Possible side effects
How to store KEXROLT
Contents of the pack and other information

1. What KEXROLT is and what it is used for

KEXROLT is a medicine used to lower elevated cholesterol levels. KEXROLT contains
ezetimibe and atorvastatin.
KEXROLT is used in adults to reduce blood levels of total cholesterol, "bad" cholesterol (LDL cholesterol), and fatty substances called triglycerides. In addition, KEXROLT increases
levels of "good" cholesterol (HDL cholesterol).
KEXROLT works in two ways to lower cholesterol. It reduces cholesterol absorbed in the
gastrointestinal tract, as well as cholesterol naturally produced by the body.
Cholesterol is one of several fatty substances found in the bloodstream. Total cholesterol is
mainly composed of LDL cholesterol and HDL cholesterol.
LDL cholesterol is often called "bad" cholesterol because it can accumulate in the walls of
arteries, forming plaques. Over time, this plaque buildup can lead to narrowing of the arteries. This narrowing can slow down or block blood flow to vital organs such as the heart and brain. This blockage of blood flow can cause a heart attack or stroke.
HDL cholesterol is often called "good" cholesterol because it helps prevent "bad" cholesterol from building up in the arteries and provides protection against heart disease.
Triglycerides are another form of fat in the blood that may increase the risk of heart disease.
KEXROLT is used to treat patients in whom diet alone is not sufficient to control cholesterol levels. While taking this medicine, you should continue to follow a cholesterol-lowering diet.
KEXROLT is used as an add-on therapy to diet to lower cholesterol if you have:

elevated cholesterol levels in the blood (primary hypercholesterolemia [heterozygous familial and non-familial]) or elevated levels of fats in the blood (mixed hyperlipidemia)
that are not adequately controlled with a statin alone;
for which you have previously been treated with a statin and ezetimibe as separate tablets.
an inherited disease (homozygous familial hypercholesterolemia) that increases your blood cholesterol levels. You may also be receiving other treatments.
heart disease. KEXROLT reduces the risk of heart attack, stroke, surgery to improve blood flow to the heart, or hospitalization for chest pain.

KEXROLT does not help with weight loss.

2. What you need to know before taking KEXROLT

Do not take KEXROLT if

you are allergic to ezetimibe, atorvastatin, or any of the other ingredients of this medicine (listed in section 6),
you have or have ever had liver disease,
you have had unexplained abnormal blood tests assessing liver function,
you are a woman of childbearing age and are not using a reliable method of contraception,
you are pregnant, trying to become pregnant, or breastfeeding,
you are taking the combination glecaprevir/pibrentasvir for the treatment of hepatitis C.

Warnings and precautions
Talk to your doctor or pharmacist before taking KEXROLT if

you have previously had a stroke with cerebral haemorrhage or if there are small accumulations of fluid in the brain due to previous strokes,
you have kidney problems,
you have an underactive thyroid gland (hypothyroidism),
you have had repeated or unexplained episodes of discomfort or muscle pain, or have a personal or family history of muscle disorders,
you have previously experienced muscle problems during treatment with other lipid-lowering medicines (e.g. other "statin" or "fibrates" medicines),
you regularly consume large amounts of alcohol,
you have a history of liver disease,
you are over 70 years old,
your doctor has told you that you have an intolerance to certain sugars, contact your doctor before taking this medicine,
you are currently taking or have taken within the last 7 days an oral or injectable medicine called fusidic acid (a medicine for bacterial infection). The combination of fusidic acid and KEXROLT can lead to serious muscle problems (rhabdomyolysis),
you have or have had myasthenia (a disease characterised by generalised muscle weakness, including in some cases the muscles used for breathing) or ocular myasthenia (a

disease causing weakness of the eye muscles), as statins may sometimes worsen
myasthenia or trigger its onset (see section 4).
Contact your doctor immediately if you experience unexplained muscle pain, tenderness, or weakness
while taking KEXROLT. This is because, in rare cases, muscle problems
can be serious, including muscle breakdown leading to kidney damage. It is known that atorvastatin can cause
muscle problems, and cases of muscle problems have also been reported with ezetimibe.
Additionally, inform your doctor or pharmacist if you have persistent muscle weakness.
Further tests and treatments may be needed to diagnose and manage this condition.
Before taking KEXROLT, discuss with your doctor or pharmacist:

if you have severe respiratory insufficiency.

If any of these conditions apply to you (or if you are unsure), consult your doctor or pharmacist
before taking KEXROLT, as your doctor may ask you to have a blood test before and possibly during
treatment with KEXROLT to assess the risk of muscle-related side effects. It is known that the risk of developing
muscle-related side effects, such as rhabdomyolysis, increases when certain medicines are taken
concurrently (see section 2 “Other medicines and KEXROLT”).
During treatment with this medicine, your doctor will monitor you carefully if you have diabetes or are at risk
of developing diabetes. You are at risk of developing diabetes if you have high levels of sugar and
fats in your blood, are overweight, or have high blood pressure.
Inform your doctor about all your medical conditions, including allergies.
The use of KEXROLT with fibrates (medicines used to lower cholesterol) should
be avoided, as the combination of KEXROLT with fibrates has not been studied.
Children
The use of KEXROLT is not recommended in children and adolescents.
Other medicines and KEXROLT
Inform your doctor or pharmacist if you are taking, have recently taken, or might take any
other medicines, including those without a prescription.
Some medicines may alter the effect of KEXROLT or their effect may be altered by KEXROLT (see section 3).
This type of interaction could reduce the effectiveness of one or both medicines. Alternatively, it could
increase the risk of side effects or their severity, including the serious condition of muscle breakdown
known as “rhabdomyolysis” described in section 4:

cyclosporine (a medicine often used in organ transplant patients),
erythromycin, clarithromycin, telithromycin, fusidic acid**, rifampicin (medicines used to treat bacterial infections),
ketoconazole, itraconazole, voriconazole, fluconazole, posaconazole (medicines used to treat fungal infections),
gemfibrozil, other fibrates, nicotinic acid, derivatives, colestipol, cholestyramine (medicines used to regulate lipid levels),
certain calcium antagonists used to treat angina or hypertension, e.g. amlodipine and diltiazem,
digoxin, verapamil, amiodarone (medicines used to regulate heart rhythm),
medicines used to treat HIV, e.g. ritonavir, lopinavir, atazanavir, indinavir, darunavir, the combination tipranavir/ritonavir, etc. (medicines for the treatment of AIDS),
certain medicines used to treat hepatitis C, e.g. telaprevir, boceprevir, and the combination elbasvir/grazoprevir,
daptomycin (a medicine used to treat complicated skin and soft tissue infections and bacteremia).

**If you need to take oral fusidic acid to treat a bacterial infection, you must
temporarily stop taking this medicine. Your doctor will tell you when it is safe
to restart treatment with KEXROLT. Taking KEXROLT with fusidic acid can
rarely lead to muscle weakness, tenderness, or pain (rhabdomyolysis). See further
information on rhabdomyolysis in section 4.

other medicines known to interact with KEXROLT,
oral contraceptives (medicines to prevent pregnancy),
stiripentol (an anticonvulsant medicine for the treatment of epilepsy),
cimetidine (a medicine used to treat heartburn and peptic ulcers),
phenazone (a painkiller),
antacids (medicines for digestive problems containing aluminium or magnesium),
warfarin, phenprocoumon, acenocoumarol, or fluindione (medicines to prevent blood clots),
colchicine (used to treat gout),
St. John’s wort (a herbal medicine used to treat depression).

KEXROLT with food and alcohol
For instructions on how to take KEXROLT, see section 3. Pay attention to the following:
Grapefruit juice
Do not drink more than one or two small glasses of grapefruit juice per day, as large quantities of
grapefruit juice may alter the effects of KEXROLT.
Alcohol
Avoid drinking excessive amounts of alcohol during treatment with this medicine. For further
information, consult section 2 “Warnings and precautions”.
Pregnancy and breastfeeding
Do not take KEXROLT if you are pregnant, planning to become pregnant, or suspect you are pregnant.
Do not take KEXROLT if you are a woman of childbearing age unless you are using an effective method of
contraception. If you become pregnant while taking KEXROLT, stop treatment immediately and
contact your doctor.
Do not take KEXROLT if you are breastfeeding.
The safety of KEXROLT during pregnancy and breastfeeding has not yet been established.
Ask your doctor or pharmacist for advice before taking this medicine.
Driving and using machines
KEXROLT is not expected to affect your ability to drive or use machines. However, you should be aware
that some people may experience dizziness after taking KEXROLT.
KEXROLT contains lactose
KEXROLT tablets contain a sugar called lactose. If your doctor has diagnosed you with an intolerance to certain sugars, contact your doctor before taking this medicine.
KEXROLT contains sodium
This medicine contains less than 1 mmol (23 mg) of sodium per tablet, i.e. essentially “sodium-free”.

3. How to take KEXROLT

Take this medicine exactly as instructed by your doctor. Your doctor will determine the appropriate tablet dosage for you based on your ongoing treatment and your individual risk profile. If you have any doubts, consult your doctor or pharmacist.

Before starting treatment with KEXROLT, you must have already begun a cholesterol-lowering diet.
During treatment with KEXROLT, you must continue to follow this cholesterol-lowering diet.

What dose to take
The recommended dose is one KEXROLT tablet taken orally once daily.
When to take the dose
Take KEXROLT at any time of day. You may take it with or without food.
If your doctor has prescribed KEXROLT together with colestyramine or another bile acid sequestrant (medicines used to lower cholesterol levels), you must take KEXROLT at least 2 hours before or 4 hours after taking the bile acid sequestrant.
If you take more KEXROLT than you should
Contact your doctor or pharmacist.
If you forget to take KEXROLT
Do not take a double dose to make up for the missed dose; take only your usual dose of KEXROLT at the next scheduled time.
If you have any questions about the use of this medicine, consult your doctor or pharmacist.

4. Possible side effects

Like all medicines, KEXROLT may cause side effects, although not everyone experiences them.
If you notice any of the following serious side effects or symptoms, stop taking the tablets immediately and contact your doctor or go to the nearest hospital emergency department without delay.

severe allergic reaction causing swelling of the face, tongue and throat, which may cause severe breathing difficulties
severe illness with extensive skin peeling and swelling, blistering of the skin, mouth, eyes, genitals, and fever; skin rash with pink-red pustules, particularly on the palms of the hands or soles of the feet, which may develop into blisters
muscle weakness, tenderness, pain or muscle breakdown, or red-brown discoloration of urine, especially if accompanied by feeling unwell and high fever; this may be due to unusual muscle breakdown, which can be life-threatening and may lead to kidney problems
lupus-like syndrome (characterized by skin rash, joint problems, and effects on blood cells)

If you experience unexpected or unusual bleeding or bruising, consult your doctor as soon as possible, as these may be signs of liver disorder.

The following common side effects have been reported (may affect up to 1 in 10 people):

diarrhoea,
muscle pain.

The following uncommon side effects have been reported (may affect up to 1 in 100 people):

influenza,
depression; difficulty falling asleep; sleep disturbances,
dizziness; headache; tingling sensation,
slow heart rate,
hot flushes,
shortness of breath,
abdominal pain; abdominal swelling; constipation; indigestion, flatulence; frequent bowel movements; stomach inflammation; nausea; stomach discomfort; stomach disorders,
acne; urticaria,
joint pain; back pain; leg cramps; fatigue, muscle spasms or weakness; pain in arms and legs,
unusual weakness; feeling tired or unwell; swelling, particularly in the ankles (oedema),
increases in certain blood test values indicating liver or muscle (CK) function,
weight gain.

The following side effects have been reported with unknown frequency (frequency cannot be estimated from available data):

myasthenia gravis (a disease causing generalized muscle weakness, including in some cases the muscles used for breathing),
ocular myasthenia (a disease causing weakness of the eye muscles).

Contact your doctor if you experience worsening weakness in the arms or legs after periods of activity, double vision or drooping eyelids, difficulty swallowing or breathlessness.

In patients treated with KEXROLT or with ezetimibe or atorvastatin tablets, the following additional side effects have also been reported:

allergic reactions including swelling of the face, lips, tongue and/or throat, which may cause difficulty breathing or swallowing (a condition requiring immediate intervention),
raised, red skin rash, sometimes accompanied by "target-like" lesions,
liver problems,
cough,
heartburn,
decreased appetite; loss of appetite,
high blood pressure,
skin rash and itching; allergic reactions including skin rashes and urticaria,
tendon injury,
gallstones or inflammation of the gallbladder (which may cause abdominal pain, nausea and vomiting),
inflammation of the pancreas, often with severe abdominal pain,
reduction in blood cell count, which may lead to bruising/bleeding (thrombocytopenia),
inflammation of the nasal passages; nosebleeds,
neck pain; pain; chest pain; sore throat,
increased or decreased blood sugar levels (if you have diabetes, you should continue to monitor your blood sugar levels closely),
nightmares,
numbness or tingling in fingers and toes,
reduced sensitivity to pain or touch,
altered sense of taste; dry mouth,
memory loss,
ringing in the ears and/or head; hearing loss,
vomiting,
belching,
hair loss,
increased body temperature,
urine tests positive for white blood cells,
blurred vision; visual disturbances,
gynaecomastia (enlargement of breast tissue in men).

Possible side effects reported with some statins:

sexual dysfunction,
depression,
breathing problems including persistent cough and/or shortness of breath or fever,
diabetes. This is more likely if you have high levels of sugar and fats in the blood, are overweight, or have high blood pressure. Your doctor will monitor you during treatment with this medicine,
muscle pain, tenderness or weakness that is persistent, and particularly if, at the same time, you feel unwell or have a high fever that does not resolve after stopping treatment with KEXROLT (frequency not known).

Reporting of side effects
If you experience any side effect, including those not listed in this leaflet, speak to your doctor or pharmacist. You can also report side effects directly via the Italian Medicines Agency (Agenzia Italiana del Farmaco) at: https://www.aifa.gov.it/content/segnalazioni-reazioni-avverse. By reporting side effects, you can help provide more information on the safety of this medicine.

5. How to store KEXROLT

Keep this medicine out of the sight and reach of children.
Do not use KEXROLT after the expiry date which is stated on the pack after “Exp.” or on the container after “EXP”. The expiry date refers to the last day of that month.
Store in the original packaging to protect the medicine from oxygen.

Do not dispose of any medicine via wastewater or household waste. Ask your pharmacist how to dispose of medicines you no longer use. This will help protect the environment.

6. Package contents and other information

What KEXROLT contains
The active substances are ezetimibe and atorvastatin. Each film-coated tablet contains 10 mg of
ezetimibe and 10 mg, 20 mg, 40 mg or 80 mg of atorvastatin (as atorvastatin calcium trihydrate).
The other components are: calcium carbonate; anhydrous colloidal silica; croscarmellose sodium;
hydroxypropylcellulose; lactose monohydrate; magnesium stearate; microcrystalline cellulose; polysorbate;
povidone; sodium lauryl sulfate.
The film coating contains: hypromellose, macrogol 8000, titanium dioxide (E171), talc.

Description of the appearance of KEXROLT and package contents
Film-coated tablets, capsule-shaped, biconvex, white to off-white in colour.
KEXROLT 10 mg/10 mg tablets: “257” engraved on one side
KEXROLT 10 mg/20 mg tablets: “333” engraved on one side
KEXROLT 10 mg/40 mg tablets: “337” engraved on one side
KEXROLT 10 mg/80 mg tablets: “357” engraved on one side

Packaging:
Blister packs (aluminum/aluminum under nitrogen, with cavity in oPA-Al-PVC and aluminum lidding foil) containing 10, 30, 90 and 100 film-coated tablets.
Blister packs (aluminum/aluminum under nitrogen, with cavity in oPA-Al-PVC and aluminum lidding foil) containing 30 x 1 and 45 x 1 film-coated tablets in single-dose blisters.

Not all pack sizes may be marketed.

Marketing Authorisation Holder and Manufacturer
Marketing Authorisation Holder
Organon Italia S.r.l.
Piazza Carlo Magno, 21
00162 Rome
Italy

Manufacturer
Merck Sharp & Dohme B.V.,
Waarderweg 39,
2031 BN Haarlem,
The Netherlands
Organon Heist bv
Industriepark 30
2220 Heist-op-den-Berg
Belgium

This medicinal product is authorised in the European Economic Area countries under the
following names:
KEXROLT: Germany, Italy