Cilozek

Poland
Brand name Cilozek
Form tablets
Active substance / Dosage
cilostazol · 100 mg
Prescription type Prescription only
ATC code
Registration number 100445006
Cilozek tablets

Package leaflet: Information for the patient

Warning! Keep this leaflet! Information on the immediate packaging is in a foreign language.
Cilozek
100 mg, tablets
Cilostazol
Please read all of this leaflet carefully before taking this medicine, because it contains
important information for the patient.

  • Keep this leaflet, as you may need to read it again.
  • If you have any further questions, please consult your doctor or pharmacist.
  • This medicine has been prescribed for a specific individual. Do not pass it on to others. This medicine may harm others, even if their symptoms are the same.
  • If you experience any adverse reactions, including any not listed in this leaflet, inform your doctor or pharmacist. See section 4.

Table of contents of the leaflet

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

1. What Cilozek is and what it is used for

Cilozek belongs to a group of medicines called phosphodiesterase type 3 inhibitors. The action of this medicine includes widening of certain blood vessels and reduction of blood clotting (aggregation) of certain blood cells called platelets. Cilozek has been prescribed for the treatment of a condition known as "intermittent claudication". Intermittent claudication is characterized by painful cramps in the legs during walking and is caused by insufficient blood supply to the legs. Cilozek helps increase the distance the patient can walk without pain, by improving blood circulation in the legs. Cilostazol is recommended only for patients in whom changes in lifestyle (such as quitting smoking and increasing physical activity) and other treatment methods have not sufficiently reduced the symptoms. It is important that the patient continues to follow the recommended lifestyle changes while taking Cilozek.

2. Important information before taking Cilozek

When not to take Cilozek

  • if the patient is allergic (hypersensitive) to cilostazol or any of the other ingredients of this medicine (listed in section 6);
  • if the patient has heart failure;
  • if the patient experiences persistent chest pain at rest, or has had a heart attack or heart surgery within the last 6 months;
  • if the patient has or has had episodes of loss of consciousness caused by heart disease, or other severe heart rhythm disorders;
  • if conditions increasing the risk of bleeding or bruising have been diagnosed in the patient, such as:
    • active peptic ulcer,
    • stroke within the last 6 months,
    • eye problems in diabetic patients,
    • inadequately controlled blood pressure disorders;
  • if the patient is concurrently taking acetylsalicylic acid and clopidogrel, or any other combination of two or more medicines that may increase the risk of bleeding (in case of any doubts, consult a doctor or pharmacist);
  • if the patient has severe kidney disease;
  • if the patient has severe or moderate liver disease;
  • if the patient is pregnant.

Warnings and precautions
Before starting treatment with Cilozek, discuss it with your doctor or pharmacist.
Inform your doctor if:

  • the patient has severe heart disorders or heart rhythm disturbances,
  • the patient has blood pressure disorders.

While taking Cilozek:

  • if the patient needs to undergo surgery, including dental procedures, the patient should inform the doctor or dentist about taking Cilozek,
  • if the patient notices an increased tendency to bruise or bleed, the medicine should be discontinued and the doctor should be informed.

Cilozek and other medicines
Tell your doctor or pharmacist about all medicines the patient is currently taking or has recently taken, as well as any medicines the patient plans to take.
In particular, inform the doctor about taking medicines used to treat pain and inflammatory conditions of muscles and joints, and about using medicines that reduce blood clotting.
Such medicines include:

  • acetylsalicylic acid,
  • clopidogrel,
  • anticoagulants (e.g. warfarin, dabigatran, rivaroxaban, apixaban, and low molecular weight heparins).

If the patient needs to take any of the above-mentioned medicines concomitantly with Cilozek, the doctor may recommend routine blood tests.
Some medicines may affect the action of Cilozek when used simultaneously.
They may either increase the risk of adverse effects of Cilozek or reduce its effectiveness.
Likewise, Cilozek may affect the action of other medicines.
Before starting treatment with Cilozek, inform the doctor if the patient is taking:

  • erythromycin, clarithromycin or rifampicin (antibiotics),
  • ketoconazole (antifungal medicine),
  • omeprazole (medicine used for excessive gastric acid secretion),
  • diltiazem (medicine used to treat hypertension and chest pain),
  • cisapride (medicine used to treat stomach disorders),
  • lovastatin, simvastatin or atorvastatin (medicines used to treat high cholesterol levels),
  • halofantrine (medicine used to treat malaria),
  • pimozide (medicine used to treat psychiatric disorders),
  • ergot alkaloids (medicines used to treat migraine, e.g. ergotamine, dihydroergotamine),
  • carbamazepine or phenytoin (antiepileptic medicines),
  • St John's wort (herbal medicine).

If in doubt whether any of the above situations applies to the patient, consult a doctor or pharmacist.
Before starting treatment with Cilozek, inform the doctor if the patient is taking medicines that lower blood pressure, because Cilozek may have an additional blood pressure-lowering effect. If blood pressure drops too low, it may cause rapid heartbeat. Medicines that lower blood pressure include:

  • diuretics (e.g. hydrochlorothiazide, furosemide),
  • calcium channel blockers (e.g. verapamil, amlodipine),
  • ACE inhibitors (e.g. captopril, lisinopril),
  • angiotensin II receptor blockers (e.g. valsartan, candesartan),
  • beta-blockers (e.g. labetalol, carvedilol).

In many cases, it is possible to take the above-mentioned medicines together with Cilozek.
The doctor will decide which medicines the patient may take.

Cilozek with food and drink
The medicine should be taken 30 minutes before breakfast and 30 minutes before the evening meal.
Tablets should always be swallowed with water.

Pregnancy, breastfeeding and fertility
Cilozek MUST NOT be used during pregnancy.
USE OF Cilozek IS NOT RECOMMENDED during breastfeeding.
If the patient is pregnant or breastfeeding, suspects she may be pregnant, or is planning a pregnancy, she should consult a doctor or pharmacist before using this medicine.

Driving and operating machinery
Cilozek may cause dizziness. If dizziness occurs after taking the medicine, DO NOT drive or operate tools or machinery. Inform your doctor or pharmacist about this.

3. How to take Cilozek

This medicine should always be taken according to the doctor's instructions. If in doubt, consult your
doctor or pharmacist.
The recommended dose is one 100 mg tablet taken twice daily (one tablet in the morning and one in
the evening). There is no need to adjust the dosage in elderly patients.
However, your doctor may reduce the dose if you are taking other medicines that may affect the action
of Cilozek. The medicine should be taken 30 minutes before breakfast and 30 minutes before the
evening meal. Tablets should always be swallowed with water.
Sometimes, the benefits of treatment with Cilozek become noticeable within 4–12 weeks of
treatment. After 3 months, the doctor will assess treatment progress and may recommend
discontinuation of cilostazol if treatment effects are insufficient.
Use in children and adolescents
Cilozek is not indicated for use in children.
Taking more Cilozek than recommended
If for any reason a patient takes more Cilozek tablets than prescribed, the following symptoms may
occur: severe headache, diarrhea, low blood pressure, and heart rhythm disturbances.
If a patient has taken more tablets than prescribed, seek medical advice immediately or go to the
nearest hospital. Remember to bring the packaging along so that it is clear which medicine has been
taken.
Missed dose of Cilozek
If a dose of Cilozek is missed, do not be alarmed. Wait until the next scheduled dose and take the
recommended dose as directed. DO NOT take a double dose to make up for the missed dose.
Stopping Cilozek
If a patient stops taking Cilozek, leg pain may return or worsen. For this reason, Cilozek should only
be discontinued if the patient experiences adverse reactions requiring immediate medical attention
(see section 4) or if otherwise advised by the doctor.
If you have any further questions about the use of this medicine, consult your doctor or pharmacist.

4. Possible adverse reactions

Like all medicines, this medicine can cause adverse reactions, although not everyone will experience them.
The frequency of adverse reactions is defined as follows:
Very common: occurs in more than 1 in 10 patients
Common: occurs in less than 1 in 10 patients
Uncommon: occurs in less than 1 in 100 patients
Rare: occurs in less than 1 in 1,000 patients
Very rare: occurs in less than 1 in 10,000 patients
Frequency not known: frequency cannot be estimated from available data.

If any of the following adverse reactions occur, the patient may require
immediate medical attention. The medicine should be discontinued immediately,
contact a doctor or go to the nearest hospital:

  • stroke,
  • heart attack,
  • heart disorders causing shortness of breath or swelling in the ankles,
  • irregular heartbeat (new onset or worsening of existing condition),
  • bleeding,
  • tendency to develop bruises,
  • severe illness with blistering rash on the skin, mouth, eyes, and genital organs,
  • yellowing of the skin and whites of the eyes due to liver or blood disorders (jaundice).

You should also contact your doctor immediately if fever or sore throat occurs.
Blood tests may be necessary, and further treatment will be decided by the doctor.
The following adverse reactions have been reported during treatment with
Cilozek.
Contact your doctor immediately:

Very common adverse reactions (may affect more than 1 in 10 people)

  • headache,
  • abnormal stools,
  • diarrhoea.

Common adverse reactions (may affect less than 1 in 10 people)

  • rapid heartbeat,
  • palpitations,
  • chest pain,
  • dizziness,
  • sore throat,
  • cold (nasal congestion),
  • abdominal pain,
  • discomfort in the stomach (dyspepsia),
  • nausea or vomiting,
  • loss of appetite (anorexia),
  • excessive belching or gas (bloating with flatulence),
  • swelling of the ankles, feet, and face,
  • rash or skin changes,
  • itching,
  • purpuric skin spots,
  • general weakness.

Uncommon adverse reactions (may affect less than 1 in 100 people)

  • heart attack,
  • irregular heartbeat (new onset or worsening of existing condition),
  • heart disorders causing shortness of breath or swelling in the ankles,
  • pneumonia,
  • cough,
  • chills,
  • unexpected bleeding,
  • tendency to bleed (e.g. gastrointestinal tract, eye or muscle, nosebleeds, blood in sputum or urine),
  • decreased number of red blood cells,
  • dizziness upon changing to an upright position,
  • fainting,
  • anxiety,
  • difficulty sleeping,
  • nightmares,
  • allergic reactions,
  • pain or discomfort,
  • diabetes and increased blood sugar levels,
  • abdominal pain (gastritis),
  • malaise.

Patients with diabetes may have an increased risk of bleeding inside the eyeball.

Rare adverse reactions (may affect less than 1 in 1,000 people)

  • tendency for bleeding to last longer than usual,
  • increased number of red blood cells,
  • kidney function disorders.

Adverse reactions observed during treatment with Cilozek, with unknown frequency of occurrence:

  • changes in blood pressure,
  • decreased number of red blood cells, white blood cells, and platelets,
  • difficulty breathing,
  • difficulty moving,
  • fever,
  • hot flushes,
  • skin rash and eruptions,
  • reduced skin sensitivity to stimuli,
  • nasal congestion, conjunctivitis,
  • tinnitus (ringing in the ears),
  • liver disorders, including hepatitis,
  • changes in urine.

Reporting of adverse reactions
If any adverse reactions occur, including any not listed in this leaflet, inform your doctor or pharmacist. Adverse reactions can be reported directly to the Department of Monitoring Adverse Drug Reactions of the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, Al. Jerozolimskie 181C, 02-222 Warsaw, phone: +48 22 49 21 301, fax: +48 22 49 21 309; website: https://smz.ezdrowie.gov.pl.
Reporting adverse reactions helps provide more information on the safety of this medicine.

5. How to store Cilozek

Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date stated on the packaging.
The expiry date refers to the last day of the stated month.
No special storage conditions apply.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer in use. This will help protect the environment.

6. Contents of the packaging and other information

What Cilozek contains

  • The active substance is cilostazol. Each tablet contains 100 mg of cilostazol.
  • The other ingredients are: corn starch, microcrystalline cellulose, calcium carmellose, hypromellose, and magnesium stearate.

What Cilozek looks like and contents of the pack
Cilozek is a white or almost white, round, flat tablet, marked with the characters "100" on one side.
Cilozek is available in packs of 30 or 60 tablets, packed in PVC/PVDC/Aluminium blisters, in a cardboard carton.
For more detailed information, please contact the Marketing Authorisation Holder or the Parallel Importer.
Marketing Authorisation Holder in Hungary, country of export:
Adamed Pharma S.A., Pieńków, ul. M. Adamkiewicza 6A, 05-152 Czosnów, Poland
Manufacturer:
Adamed Pharma S.A., Pieńków, ul. M. Adamkiewicza 6A, 05-152 Czosnów, Poland
Parallel Importer:
InPharm Sp. z o.o., ul. Strumykowa 28/11, 03-138 Warsaw, Poland
Repackaged by:
InPharm Sp. z o.o. Services sp. k., ul. Chełmżyńska 249, 04-458 Warsaw, Poland
Marketing Authorisation numbers in Hungary, country of export: OGYI-T-22653/08
OGYI-T-22653/06
Parallel Import Marketing Authorisation number: 11/21
This medicinal product is authorised for sale in the Member States of the European Economic Area under the following names:

EstoniaCilozek
PolandCilozek
Czech RepublicCilozek
SlovakiaCilozek 100 mg tablets
HungaryCilozek 100 mg tablet
SpainCilostazol Viatris 100 mg tablets EFG
GreeceINCLAUD 100 mg tablets
RomaniaVELYN 100 mg tablets