АТЕНОЛОЛО 100 мг/25 мг Таблетки

Содержание инструкции

1. ATENOLOLO CLORTALIDONE EG 50 mg + 12,5 mg tablets
   1. What is ATENOLOLO CLORTALIDONE EG and what it is used for
   2. What you need to know before taking ATENOLOLO CLORTALIDONE EG
   3. How to take ATENOLOLO CLORTALIDONE EG
   4. Possible side effects
   5. How to store ATENOLOLO CLORTALIDONE EG
   6. Contents of the pack and other information
2. ATENOLOLO CLORTALIDONE EG 100 mg + 25 mg tablets
   1. What is ATENOLOLO CLORTALIDONE EG and what it is used for
   2. What you need to know before taking ATENOLOLO CLORTALIDONE EG
   3. How to take ATENOLOLO CLORTALIDONE EG
   4. Possible side effects
   5. How to store ATENOLOLO CLORTALIDONE EG
   6. Contents of the pack and other information

ATENOLOLO CLORTALIDONE EG 50 mg + 12,5 mg tablets

Equivalent Medicinal Product

Read this leaflet carefully before taking this medicine as 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 pass it on to others, even if they have the same symptoms as you, as it may be harmful.
• If any side effects occur, including those not listed in this leaflet, tell your doctor or pharmacist. See section 4.

Contents of this leaflet:

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

1. What is ATENOLOLO CLORTALIDONE EG and what it is used for

This medicine contains two active ingredients, atenolol and chlortalidone.
Atenolol belongs to a group of medicines called beta-blockers, which work by slowing down the heartbeat
and making the heart beat with less force.
Chlortalidone belongs to a group of medicines called diuretics which work by increasing the amount
of urine produced by the kidneys.
These two active ingredients work together to lower blood pressure.
ATENOLOLO CLORTALIDONE EG is indicated for the treatment of high blood pressure
(essential hypertension) when blood pressure is not adequately controlled by therapy with the
individual active ingredients (atenolol and chlortalidone).

2. What you need to know before taking ATENOLOLO CLORTALIDONE EG

Do not take ATENOLOLO CLORTALIDONE EG

• if you are allergic to atenolol or clortalidone (or to medicines derived from sulfonamides) or to any of the other ingredients of this medicine (listed in section 6);
• if you have a very irregular heartbeat (sick sinus syndrome) or if you suffer from certain heart conduction diseases (second or third degree atrioventricular block);
• if you have a very slow heartbeat (bradycardia) (<55 beats per minute);< li>
• if your heart function is insufficient and is not controlled by adequate therapy (uncontrolled heart failure);
• if you have a severe heart problem, known as cardiogenic shock, which occurs when your heart does not pump enough blood throughout the body;
• if you have low blood pressure (hypotension);
• if you have severe disturbances of blood circulation in the limbs (peripheral arterial circulation);
• if you have severe kidney problems (severe renal failure);
• if your doctor has told you that the level of acidity in your blood is higher than normal (metabolic acidosis);
• if you have a tumor of the adrenal gland, called “pheochromocytoma” that has not been treated;
• if you have severe liver and kidney problems (hepatopathies and nephropathies);
• if you suffer from an inflammatory type of joint disease (manifest gout);
• if you are pregnant and if you are breastfeeding;
• if you are taking medicines such as verapamil (used to treat high blood pressure).

Warnings and precautions
Talk to your doctor or pharmacist before taking ATENOLOLO CLORTALIDONE EG.
Pay particular attention and consult your doctor:

• if your heart function is insufficient (heart failure), but is kept under control by adequate therapy;
• if your heart's ability to increase the amount of blood pumped into the body is poor (poor cardiac reserve);
• if you suffer from chest pain called Prinzmetal's angina, as this medicine may increase the number and duration of angina attacks;
• if you have disturbances of blood circulation in the limbs;
• if you have heart problems (first-degree atrioventricular block, a disease of the heart's conduction system);
• if you have suffered from ischemic heart disease, a heart disease that occurs when there is insufficient oxygenation of the heart muscle. Consult your doctor before stopping treatment with ATENOLOLO CLORTALIDONE EG;
• if you have had severe allergic reactions (anaphylactic reactions) in the past;
• if you suffer from respiratory diseases. If you experience a worsening of symptoms, stop treatment and inform your doctor;
• if you are using eye drops based on similar active ingredients (beta-blockers);
• if you are to undergo anesthesia for surgery. Inform the anesthesiologist that you are taking ATENOLOLO CLORTALIDONE EG;
• if you are being treated for a type of tumor called pheochromocytoma, in this case your blood pressure will need to be closely monitored during treatment;
• if you have problems with your thyroid gland (thyrotoxicosis), because atenolol may mask its cardiovascular symptoms;
• if you have diabetes or a predisposition to diabetes, because atenolol may alter the signals of a low blood sugar level (hypoglycemia) such as a fast heartbeat, palpitations and sweating, while clortalidone may cause an increase in blood sugar levels (hyperglycemia);
• if you suffer from liver disorders (impaired liver function or progressive liver disease);
• if you are elderly, if you suffer from heart problems (heart failure) and are being treated with medicines belonging to the group of digitalis glycosides, if you follow a low-potassium diet or if you suffer from stomach and intestinal disorders, because a reduction in potassium and sodium levels in the blood (hypokalemia and hyponatremia) may occur.

During treatment with this medicine, periodically perform blood tests to be able to
identify any changes in salt levels (especially low levels of potassium and sodium) and, if
necessary, to check uric acid levels, because an increase in uricemia may occur. It is
recommended to also periodically check the sugar level in the urine.
During treatment with this medicine, a reduction in heart rate is normal,
however if it is excessive, consult your doctor who will reduce the dosage.
If you play sports: the use of this medicine without a therapeutic need constitutes doping and may
anyway determine positivity to doping tests.

Other medicines and ATENOLOLO CLORTALIDONE EG
Tell your doctor or pharmacist if you are taking, have recently taken or might take any
other medicines.
Do not take this medicine if you have been given calcium channel blockers (e.g. verapamil or
diltiazem) by intravenous injection in the last 48 hours.
Pay particular attention and consult your doctor if you are taking:

• medicines used to treat heart rhythm disturbances (disopyramide, amiodarone, digitalis glycosides);
• clonidine, a medicine used to treat high blood pressure. If the two drugs are administered simultaneously, this medicine must be discontinued several days before stopping therapy with clonidine. If therapy with ATENOLOLO CLORTALIDONE EG is to replace that with clonidine, the start of treatment must take place several days after stopping therapy with clonidine;
• medicines used to treat high blood pressure belonging to the dihydropyridine group (e.g. nifedipine);
• medicines that stimulate the heart belonging to the sympathomimetic group (e.g. adrenaline);
• medicines used in case of inflammation and to relieve pain (e.g. ibuprofen, indometacin);
• baclofen, a medicine used to treat muscle disorders. Dose adjustments may be necessary;
• lithium, a medicine used to treat mental disorders. Dose adjustment of lithium may be necessary;
• medicines used to induce anesthesia (See section Warnings and precautions);
• some medicines used to facilitate the elimination of urine (thiazide diuretics).

Pregnancy and breastfeeding
If you are pregnant, suspect you may be pregnant, are planning to become pregnant, or are breastfeeding,
ask your doctor or pharmacist for advice before taking this medicine.
Do not use this medicine if you are pregnant and if you are breastfeeding.

Driving and using machines
The use of this medicine may cause side effects such as fatigue and dizziness. If this happens to you,
avoid driving vehicles or using machines.

3. How to take ATENOLOLO CLORTALIDONE EG

Take this medicine following exactly the instructions of your doctor or pharmacist. If you have
doubts, consult your doctor or pharmacist.
The recommended dose in adults is one tablet a day. If this dose should not be effective, it is
necessary to increase the dosage (to one tablet of ATENOLOLO CLORTALIDONE EG 100 mg + 25
mg tablets) or associate another medicine, such as a vasodilator, to lower blood
pressure.
If you are already being treated with other antihypertensive medicines, you may switch directly to using this
medicine, with the exception of preparations based on clonidine (see section Other medicines and
ATENOLOLO CLORTALIDONE EG).

Use in the elderly
If you are elderly, your doctor will adjust the dosage or prescribe you another medicine at reduced doses
(vasodilator medicines).

Use in patients with severe kidney problems
If you have severe kidney problems (severe renal insufficiency) do not take this medicine (See Do not take
ATENOLOLO E CLORTALIDONE EG).

Use in patients with liver problems
If you suffer from liver problems, it is not necessary to change the dose.

Use in children and adolescents
There is no experience on the use of ATENOLOLO CLORTALIDONE EG in children and adolescents.
Therefore ATENOLOLO CLORTALIDONE EG is not recommended in children and adolescents.

If you take more ATENOLOLO CLORTALIDONE EG than you should
Following the intake of an excessive dose of this medicine, the following
symptoms may occur:

• slowing of the heartbeat (bradycardia);
• decrease in blood pressure (hypotension);
• insufficient heart function (acute heart failure);
• difficulty breathing (bronchospasm).

In case of ingestion/intake of an excessive quantity of this medicine, immediately contact
your doctor or the Emergency Room of the nearest hospital.

If you forget to take ATENOLOLO CLORTALIDONE EG
If you forget to take a tablet, do so as soon as you remember, unless it is almost time to
take the next dose. Do not take a double dose to make up for the forgotten tablet.

If you stop taking ATENOLOLO CLORTALIDONE EG
Discontinuation of treatment must occur gradually, especially if you suffer from disorders of
heart blood circulation (ischemic heart disease).
If you have any doubts about the use of this medicine, consult your doctor or pharmacist.

4. Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them.
The following side effects may occur:

Common(may affect up to 1 in 10 people)

• slowing of the heartbeat (bradycardia);
• feeling of coldness in the hands and feet;
• stomach and intestinal disorders, including nausea;
• fatigue;
• high level of uric acid in the blood (hyperuricemia);
• low levels of sodium and potassium in the blood (hyponatremia and hypokalemia);
• reduced glucose tolerance.

Uncommon(may affect up to 1 in 100 people)

• sleep disorders;
• increased levels of transaminases.

Rare(may affect up to 1 in 1000 people)

• skin disease manifesting with the appearance of blisters that tend to bleed (purpura);
• reduction of the number of platelets and white blood cells (thrombocytopenia and leukopenia);
• mood changes;
• nightmares, confusion, mental disorders (psychosis and hallucinations);
• dizziness and headache;
• tingling in the hands and feet (paresthesia);
• visual disturbances, dry eyes;
• worsening of heart function (heart failure) and blockage of heart function;
• sudden drop in blood pressure when getting up, with possible loss of consciousness (syncope);
• worsening of movement difficulty (intermittent claudication);
• circulation problems in the hands and feet (Raynaud's phenomenon);
• dry mouth;
• difficulty breathing (bronchospasm), in people who suffer from bronchial asthma or who have suffered from asthma;
• liver problems, including alterations in bile flow (intrahepatic cholestasis) and inflammation of the pancreas (pancreatitis);
• hair loss (alopecia);
• skin inflammations, worsening of psoriasis, skin rash;
• difficulty achieving or maintaining an erection (impotence).

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

• increase in antinuclear antibodies, a type of autoantibody that the body produces against itself.

Not known(frequency cannot be estimated from available data)

• constipation,
• lupus-like syndrome (a disease in which the immune system produces antibodies that primarily attack the skin and joints).

Reporting of side effects
If you get any side effects, even those not listed in this leaflet, tell your
doctor or pharmacist. You can also report side effects directly through the national reporting system at www.agenziafarmaco.gov.it/it/responsabili . By reporting side
effects you can help provide more information on the safety of this medicine.

5. How to store ATENOLOLO CLORTALIDONE EG

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 packaging after “Exp”.
The expiry date refers to the last day of that month.
This medicine does not require any particular storage conditions.
Do not dispose of any medicine in wastewater or household waste. Ask your pharmacist how to dispose of
medicines you no longer use. This will help protect the environment.

6. Contents of the pack and other information

What ATENOLOLO CLORTALIDONE EG contains

• The active ingredients are atenolol and clortalidone. Each tablet contains 50 mg of atenolol and 12.5 mg of clortalidone.
• The other ingredients are corn starch, magnesium carbonate, sodium lauryl sulfate, gelatin, magnesium stearate.

Description of the appearance of ATENOLOLO CLORTALIDONE EG and contents of the pack
Pack in blisters of 28 tablets.

Marketing Authorisation Holder
EG S.p.A., Via Pavia 6 - 20136 Milan, Italy.

Manufacturer
Doppel Farmaceutici S.r.l. - Via Volturno, 48 Quinto De’ Stampi, Rozzano (MI)
Cosmo S.p.A. Via C. Colombo, 1 - 20020 Lainate (MI)

ATENOLOLO CLORTALIDONE EG 100 mg + 25 mg tablets

Generic medicine

Read this leaflet carefully before taking this medicine as 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 pass it on to others, even if their symptoms are the same as yours, as it could be harmful.
• If you get any side effects, even those not listed in this leaflet, tell your doctor or pharmacist. See section 4.

Contents of this leaflet:

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

1. What is ATENOLOLO CLORTALIDONE EG and what it is used for

This medicine contains two active ingredients, atenolol and chlortalidone.
Atenolol belongs to a group of medicines called beta-blockers, which work by slowing down the heartbeat
and causing the heart to beat with less force.
Chlortalidone belongs to a group of medicines called diuretics which work by increasing the amount
of urine produced by the kidneys.
These two active ingredients work together to lower blood pressure.
ATENOLOLO CLORTALIDONE EG is indicated for the treatment of high blood pressure
(essential hypertension) when blood pressure is not adequately controlled by therapy with the
individual active ingredients (atenolol and chlortalidone).

2. What you need to know before taking ATENOLOLO CLORTALIDONE EG

Do not take ATENOLOLO CLORTALIDONE EG

• if you are allergic to atenolol or clortalidone (or to sulfonamide-derived medicines) or to any of the other ingredients of this medicine (listed in section 6);
• if you have a very irregular heartbeat (sick sinus syndrome) or if you suffer from certain heart conduction diseases (second or third degree atrioventricular block);
• if you have a very slow heartbeat (bradycardia) (<55 beats per minute);< li>
• if your heart function is insufficient and is not controlled by adequate therapy (uncontrolled heart failure);
• if you have a severe heart problem, known as cardiogenic shock, which occurs when your heart does not pump enough blood throughout your body;
• if you have low blood pressure (hypotension);
• if you have severe disturbances of blood circulation in the limbs (peripheral arterial circulation);
• if you have severe kidney problems (severe renal failure);
• if your doctor has told you that the level of acidity in your blood is higher than normal (metabolic acidosis);
• if you have a tumor of the adrenal gland, called “pheochromocytoma” that has not been treated;
• if you have severe liver and kidney problems (hepatopathies and nephropathies);
• if you suffer from an inflammatory type of joint disease (manifest gout);
• if you are pregnant and if you are breastfeeding with breast milk;
• if you are taking medicines such as verapamil (used to treat high blood pressure).

Warnings and precautions
Talk to your doctor or pharmacist before taking ATENOLOLO CLORTALIDONE EG.
Pay particular attention and consult your doctor:

• if your heart function is insufficient (heart failure), but is kept under control by adequate therapy;
• if your heart's ability to increase the amount of blood pumped to the body is poor (poor cardiac reserve);
• if you suffer from chest pain called Prinzmetal's angina, as this medicine may increase the number and duration of angina attacks;
• if you have disturbances of blood circulation in the limbs;
• if you have heart problems (first degree atrioventricular block, a disease of the heart's conduction system);
• if you have suffered from ischemic heart disease, a heart disease that occurs when there is insufficient oxygenation of the heart muscle. Consult your doctor before stopping treatment with ATENOLOLO CLORTALIDONE EG;
• if you have had severe allergic reactions (anaphylactic reactions) in the past;
• if you suffer from respiratory diseases. If your symptoms worsen, stop treatment and inform your doctor;
• if you are using eye drops based on similar active ingredients (beta-blockers);
• if you are to undergo anesthesia for surgery. Inform the anesthesiologist that you are taking ATENOLOLO CLORTALIDONE EG;
• if you are being treated for a tumor called pheochromocytoma, in this case your blood pressure will need to be closely monitored during treatment;
• if you have problems with your thyroid gland (thyrotoxicosis), because atenolol may mask its cardiovascular symptoms;
• if you have diabetes or a predisposition to diabetes, because atenolol may alter the signals of a low blood sugar level (hypoglycemia) such as a fast heartbeat, palpitations and sweating, while clortalidone may cause an increase in blood sugar levels (hyperglycemia);
• if you suffer from liver disorders (impaired liver function or progressive liver disease);
• if you are elderly, if you suffer from heart problems (heart failure) and are being treated with medicines belonging to the group of digitalis glycosides, if you follow a low-potassium diet or if you suffer from stomach and intestinal disorders, because a reduction in potassium and sodium levels in the blood (hypokalemia and hyponatremia) may occur.

During treatment with this medicine, periodically perform blood tests to be able to
identify any changes in the levels of salts (especially low levels of potassium and sodium) and, if
necessary, to check the levels of uric acid, because an increase in uricemia may occur. It is
recommended to also periodically check the level of sugar in the urine.
During treatment with this medicine, a reduction in heart rate is normal,
however if it is excessive, consult your doctor who will reduce the dosage.
If you play sports: the use of this medicine without a therapeutic need constitutes doping and may
anyway determine positivity to anti-doping tests.

Other medicines and ATENOLOLO CLORTALIDONE EG
Tell your doctor or pharmacist if you are taking, have recently taken or might take any
other medicine.
Do not take this medicine if you have been given calcium channel blockers (e.g. verapamil or
diltiazem) by intravenous injection in the last 48 hours.
Pay particular attention and consult your doctor if you are taking:

• medicines used to treat heart rhythm disturbances (disopyramide, amiodarone glycoside-digitalis);
• clonidine, a medicine used to treat high blood pressure. If the two drugs are administered simultaneously, this medicine must be discontinued several days before stopping therapy with clonidine. If therapy with ATENOLOLO CLORTALIDONE EG is to replace that with clonidine, it is necessary that the start of treatment occurs several days after stopping therapy with clonidine;
• medicines used to treat high blood pressure belonging to the dihydropyridine group (e.g. nifedipine);
• medicines that stimulate the heart belonging to the sympathomimetic group (e.g. adrenaline);
• medicines used in case of inflammation and to relieve pain (e.g. ibuprofen, indometacin);
• baclofen, a medicine used to treat muscle disorders. Dose adjustments may be necessary;
• lithium, a medicine used to treat mental disorders. Dose adjustment of lithium may be necessary;
• medicines used to induce anesthesia (See section Warnings and precautions);
• some medicines used to facilitate the elimination of urine (thiazide diuretics).

Pregnancy and breastfeeding
If you are pregnant, suspect you are pregnant, or are planning to become pregnant, or if you are breastfeeding with breast
milk, ask your doctor or pharmacist for advice before taking this medicine.
Do not use this medicine if you are pregnant and if you are breastfeeding with breast milk.

Driving and operating machinery
The use of this medicine may cause undesirable effects such as fatigue and dizziness. If this happens to
you, avoid driving vehicles or using machinery.

3. How to take ATENOLOLO CLORTALIDONE EG

Take this medicine following exactly the instructions of your doctor or pharmacist. If you have
any doubts, ask your doctor or pharmacist.
The recommended dose in adults is one tablet a day. If this dose is not effective, it is
necessary to associate another medicine, such as a vasodilator, to lower your blood pressure.
If you are already being treated with other antihypertensive medicines, you may switch directly to using this
medicine, except for preparations based on clonidine (see section Other medicines and
ATENOLOLO CLORTALIDONE EG).

Use in the elderly
If you are elderly, your doctor will adjust the dosage, reducing the daily dose

Use in patients with severe kidney problems
If you suffer from severe kidney problems (severe renal insufficiency) do not take this medicine (see Do
not take ATENOLOLO CLORTALIDONE EG).

Use in patients with liver problems
If you suffer from liver problems, it is not necessary to change the dose.

Use in children and adolescents
There is no experience with the use of ATENOLOLO CLORTALIDONE EG in children and adolescents.
Therefore, ATENOLOLO CLORTALIDONE EG is not recommended in children and adolescents.

If you take more ATENOLOLO CLORTALIDONE EG than you should
Following the intake of an excessive dose of this medicine, the following
symptoms may occur:

• slowing of the heartbeat (bradycardia);
• decrease in blood pressure (hypotension);
• insufficient heart function (acute heart failure);
• difficulty breathing (bronchospasm).

In case of ingestion/intake of an excessive amount of this medicine, contact your doctor or the Emergency Room of the
nearest hospital immediately.

If you forget to take ATENOLOLO CLORTALIDONE EG
If you forget to take a tablet, take it as soon as you remember, unless it is almost time to
take the next dose. Do not take a double dose to make up for the forgotten tablet.

If you stop taking ATENOLOLO CLORTALIDONE EG
Discontinuation of treatment must be gradual, especially if you suffer from disorders of
heart blood circulation (ischemic heart disease).
If you have any doubts about 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.
The following side effects may occur:

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

• slowing of the heartbeat (bradycardia);
• feeling of coldness in the hands and feet;
• stomach and intestinal disorders, including nausea;
• fatigue;
• high level of uric acid in the blood (hyperuricemia);
• low levels of sodium and potassium in the blood (hyponatremia and hypokalemia);
• reduced glucose tolerance.

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

• sleep disorders;
• increased levels of transaminases.

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

• skin disease manifesting with the appearance of blisters that tend to bleed (purpura);
• reduction in the number of platelets and white blood cells (thrombocytopenia and leukopenia);
• changes in mood;
• nightmares, confusion, mental disorders (psychosis and hallucinations);
• dizziness and headache;
• tingling in the hands and feet (paresthesia);
• vision disorders, dry eyes;
• worsening of heart function (heart failure) and blockage of heart function;
• sudden drop in blood pressure when standing up with possible loss of consciousness (syncope);
• worsening of movement difficulty (intermittent claudication);
• circulation problems in the hands and feet (Raynaud's phenomenon);
• dry mouth;
• difficulty breathing (bronchospasm), in people who suffer from bronchial asthma or who have suffered from asthma;
• liver problems, including alterations in bile flow (intrahepatic cholestasis) and inflammation of the pancreas (pancreatitis);
• hair loss (alopecia);
• skin inflammation, worsening of psoriasis, skin rash;
• difficulty achieving or maintaining an erection (impotence).

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

• increase in antinuclear antibodies, a type of autoantibody that the body produces against itself.

Not known(frequency cannot be estimated from available data):

• constipation,
• lupus-like syndrome (a disease in which the immune system produces antibodies that primarily attack the skin and joints).

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 through the national reporting system at www.agenziafarmaco.gov.it/it/responsabili. By reporting side effects you can help provide more information on the safety of this medicine.

5. How to store ATENOLOLO CLORTALIDONE EG

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 packaging after “Exp”.
The expiry date refers to the last day of that month.
This medicine does not require any particular storage conditions.
Do not dispose of any medicine in waste water or household waste. Ask your pharmacist how to dispose of
medicines you no longer use. This will help protect the environment.

6. Contents of the pack and other information

What ATENOLOLO CLORTALIDONE EG contains

• The active ingredients are atenolol and clortalidone. Each tablet contains 100 mg of atenolol and 25 mg of clortalidone.
• The other ingredients are corn starch, magnesium carbonate, sodium lauryl sulfate, gelatin, magnesium stearate.

Description of the appearance of ATENOLOLO CLORTALIDONE EG and contents of the pack
Pack with 28 tablets in blisters.

Marketing Authorisation Holder
EG S.p.A., Via Pavia 6, - 20136 Milan, Italy

Manufacturer
Doppel Farmaceutici S.r.l. – Via Volturno, 48 Quinto De’ Stampi, Rozzano (MI)
Cosmo S.p.A. Via C. Colombo, 1 - 20020 Lainate (MI)