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Voltaren retard 100 mg comprimidos de liberacion modificada

О препарате

Introduction

Package Leaflet: Information for the User

Voltarén Retard 100 mg Modified Release Tablets

Diclofenac Sodium

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

  • Keep this leaflet, as 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 harm them.
  • If you experience any side effects, talk to your doctor or pharmacist. See section 4.

1. What is Voltarén Retard 100 mg and what is it used for

2. What you need to know before you take Voltarén Retard 100 mg

3. How to take Voltarén Retard 100 mg

4. Possible side effects

5. Storage of Voltarén Retard 100 mg

6. Contents of the pack and additional information

1. What is Voltarén Retard 100 mg and what is it used for

Sodium diclofenac, the active ingredient ofVoltarén Retard belongs to the group of medicines called non-steroidal anti-inflammatory drugs, used to treat pain and inflammation.

Voltarén Retard is used to treat the following conditions:

-Chronic inflammatory rheumatic diseases (rheumatoid arthritis, ankylosing spondylitis, osteoarthritis),

-Extra-articular rheumatism,

-Acute gout attacks,

-M menstrual pains,

-Post-traumatic inflammation.

2. What you need to know before starting to take Voltarén Retard 100 mg

It is essential to use the smallest effective dose to relieve or control pain and not to take this medication for longer than necessary to control your symptoms.

No take Voltarén Retard

  • if you are allergic to diclofenac sodium or any of the other components of this medication (listed in section 6).
  • if you are allergic or have had allergic reactions to acetylsalicylic acid or other analgesics (pain medications) similar to it. Allergic reactions may include asthma (difficulty breathing), chest pain, urticaria (skin reaction with itching), acute rhinitis (inflammation of the nasal mucosa), or swelling of the face, lips, tongue, throat, and/or extremities (signs of angioedema). If you think you may be allergic, consult your doctor.
  • if you have had a previous gastrointestinal hemorrhage or have suffered two or more instances of a perforated digestive tract while taking a nonsteroidal anti-inflammatory drug.
  • if you currently have or have had more than one instance of a stomach or duodenal ulcer
  • if you have active Crohn's disease or ulcerative colitis (diseases that produce diarrhea with or without blood and abdominal pain).
  • if you have severe kidney disease.
  • if you have severe liver disease.
  • if you have established cardiovascular disease and/or cerebrovascular disease, for example, if you have had a heart attack, stroke, mini-stroke (TIA), or blockages in the heart or brain blood vessels, or a surgery to remove an obstruction or perform a coronary bypass.
  • if you have or have had peripheral arterial disease (circulation problems).
  • if you are in the third trimester of pregnancy.
  • if you have bleeding disorders.

Ensure that your doctor knows:

  • if you smoke
  • if you have diabetes
  • if you have angina, blood clots, high blood pressure, high cholesterol, or high triglycerides

The adverse effects can be minimized by using the lowest effective dose for the shortest possible period.

Warnings and precautions

Consult your doctor or pharmacist before starting to take Voltarén Retard:

-if you have had or develop a stomach or duodenal ulcer, hemorrhage, or perforation, which may manifest as intense or persistent abdominal pain and/or black stools, even without previous warning symptoms.

This risk is higher when using high doses and prolonged treatments in patients with a history of peptic ulcer disease and in the elderly. In these cases, your doctor will consider the possibility of associating a stomach protector medication.

-if you have any of the following conditions: asthma, mild heart disease, liver disease, kidney disease, high blood pressure (hypertension), bleeding disorders, or other blood disorders, including porphyria hepatica.

-if you are taking blood pressure medications or ciclosporin, as this increases the risk of kidney damage (see "Other medications and Voltarén Retard").

  • if you take medications that alter blood coagulation or increase the risk of ulcers, such as oral anticoagulants or antiplatelet agents like acetylsalicylic acid. You should also inform your doctor about the use of other medications that may increase the risk of bleeding, such as other nonsteroidal anti-inflammatory drugs, corticosteroids, and selective serotonin reuptake inhibitors (SSRIs) (see "Other medications and Voltarén Retard").
  • if you have Crohn's disease or ulcerative colitis, as Voltarén-type medications may worsen these conditions.
  • if you have high blood pressure, high cholesterol, or triglycerides, diabetes, or are a smoker (cardiovascular risk factors), your doctor will reevaluate whether you should continue treatment with this medication, especially if you have been taking it for more than 4 weeks.
  • if you have liver insufficiency, kidney insufficiency, or bleeding disorders, you will need to have frequent blood tests during treatment. This will allow your doctor to control the functioning of your liver (transaminase levels), kidneys (creatinine levels), or blood (lymphocyte, erythrocyte, and platelet levels). Your doctor will then decide whether to interrupt or change the dose of this medication.
  • if you have recently undergone or are about to undergo surgical intervention on the stomach or intestine before taking this medication, as this medication may sometimes worsen the healing of intestinal wounds after surgery.

Patients with cardiovascular problems

Medications like Voltarén Retard may be associated with an increased risk of heart attacks or strokes, especially when used in high doses and for prolonged periods. Do not exceed the recommended dose or treatment duration.

If you have heart problems, a history of strokes, or think you may be at risk (for example, you have high blood pressure, diabetes, high cholesterol, or are a smoker) and your doctor decides to treat you with this medication, do not take more than 100 mg per day if the treatment lasts more than 4 weeks.

This type of medication may also cause fluid retention, especially in patients with heart disease and/or high blood pressure.

In general, it is very important to take the lowest effective dose of this medication for the shortest possible time to relieve pain and/or inflammation to reduce the risk of cardiovascular adverse effects.

If you experience chest pain, shortness of breath, weakness, or difficulty speaking while taking this medication, contact your doctor immediately.

Other medications and Voltarén Retard

Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any other medication.

Certain medications may interact with Voltarén Retard; in these cases, you may need to change the dose or interrupt treatment with one of them.

It is essential to inform your doctor if you are taking or have taken recently any of the following medications:

  • medications containing lithium or selective serotonin reuptake inhibitors (SSRIs) (for treating certain types of depression),
  • medications containing methotrexate (for treating rheumatoid arthritis and cancer),
  • medications containing ciclosporin, tacrolimus (after transplants),
  • medications containing trimethoprim (for preventing and treating urinary tract diseases),
  • medications for heart problems (digoxin, calcium channel blockers such as verapamil or isradipine),
  • medications used to treat diabetes, except for insulin,
  • medications for controlling blood pressure (diuretics, beta blockers, and ACE inhibitors),
  • medications for preventing blood clots,
  • medications containing quinolone or ceftriaxone (for treating infections),
  • other medications in the same group as Voltarén (nonsteroidal anti-inflammatory drugs) such as acetylsalicylic acid or ibuprofen,
  • corticosteroids (medications that reduce inflammation and immune system activity),
  • medications containing voriconazole (a medication used to treat fungal infections),
  • medications containing phenytoin (a medication used to treat seizures),
  • medications containing misoprostol (for treating stomach ulcers),
  • medications containing cholestyramine and colestipol to lower cholesterol levels in the blood),
  • medications containing pentazocine (for relieving pain),
  • antibiotic medication used to treat bacterial infections (rifampicin).

Taking Voltarén Retard with food, drinks, and alcohol

You can take this medication with or without food, as food does not affect the effect of this medication.

Consuming alcoholic beverages with this medication may increase its toxicity.

Children and adolescents

This medication is not recommended for children and adolescents.

Older adults

Older adults, especially those who are more fragile or have a low body weight, may be more sensitive to the effects of this medication than the general adult population. Therefore, it is especially important for older adults to inform their doctor immediately about any adverse effects they experience.

Pregnancy, breastfeeding, and fertility

If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medication.

Pregnancy

Do not take this medication if you are in the last 3 months of pregnancy, as it may harm the fetus or cause problems during delivery. It may cause kidney and heart problems in your fetus. It may affect your tendency and that of your baby to bleed and delay or prolong delivery more than expected. Do not take this medication during the first 6 months of pregnancy unless it is clearly necessary and as indicated by your doctor. If you need treatment during this period or while trying to become pregnant, you should take the minimum dose for the shortest possible time. If you take it for more than a few days after week 20 of pregnancy, this medication may cause kidney problems in your fetus, which may cause low amniotic fluid levels surrounding the baby (oligohydramnios) or narrowing of a blood vessel (ductus arteriosus) in the baby's heart. If you need treatment for a period longer than a few days, your doctor may recommend additional monitoring.

Breastfeeding

Small amounts of diclofenac may appear in breast milk, so you should not take this medication while breastfeeding.

Fertility

For women of childbearing age, it is essential to consider that medications like Voltarén Retard have been associated with a decrease in the ability to conceive.

Driving and operating machinery

The influence of diclofenac on the ability to drive and operate machinery is negligible or insignificant. However, patients who experience visual disturbances, dizziness, vertigo, somnolence, or other central nervous system disorders while taking Voltarén Retard should avoid driving vehicles or operating machinery.

Voltarén Retard contains saccharose and sodium.

This medication contains saccharose; if your doctor has indicated that you have an intolerance to certain sugars, consult with them before taking this medication.

This medication contains less than 23 mg of sodium (1 mmol) per tablet; it is essentially "sodium-free".

3. How to Take Voltarén Retard 100 mg

Follow exactly the administration instructions for this medication as indicated by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.

Remember to take your medication.

Use in adults

The usual dose in mild cases or in prolonged treatments is1 tablet of 100 mg per day.

In menstrual cramps, the daily dose, which should be adjusted individually, is 50-200 mg of diclofenac (1 to 2 tabletsof Voltarén Retard 100 mg).A starting dose of 50-100 mg of diclofenac (1 tabletof Voltarén Retard 100 mg) should be administered and, if necessary, increased in subsequent menstrual cycles. Treatment should begin when the first symptom appears. Depending on its intensity, it should be continued for a few days. For a 50 mg dose, the use of Voltarén 50 mg gastro-resistant tablets is recommended, and for doses of 75 and 150 mg, Voltarén Retard 75 mg tablets.

Administration form

This medication can be takenwith or without food(see section “Taking Voltarén Retard with food, drinks, and alcohol”).

The tablets should be swallowed whole with a glass of water or another liquid, without dividing or chewing them.

If you take more Voltarén Retard than you should

In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the toxicology information service. Phone 91.562.04.20.

If you forget to take Voltarén Retard

Do not take a double dose to compensate for the missed doses.

If you forget to take a dose, take it as soon as you can, except if it is almost time for the next one; then return to the usual administration schedule. If you forget several doses, consult your doctor.

If you have any other doubts about the use of this medication, consult your doctor or pharmacist.

If you interrupt treatment with VoltarénRetard

Your doctor will indicate the duration of your treatment with this medication. Do not stop treatment before.

4. Possible Adverse Effects

Like all medicines, this medicine can cause side effects, although not everyone will experience them.

Some side effects can be serious.

Stop using this medicine and immediately inform your doctor if you notice:

Mild abdominal cramps and abdominal pain to palpation that begins shortly after starting treatment with this medicine followed by rectal bleeding or bloody diarrhea observed normally within 24 hours after the onset of abdominal pain (with unknown frequency, cannot be determined from available data).

Chest pain, which can be a sign of a potentially severe allergic reaction called Kounis syndrome.

Other side effects that have been reported with the use of this medicine are:

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

Nervous system disorders

  • headache
  • dizziness

Vestibular disorders

  • vertigo

Gastrointestinal disorders

  • nausea
  • vomiting
  • diarrhea
  • heartburn
  • abdominal pain
  • gas
  • loss of appetite

Hepatobiliary disorders

  • alterations in liver function test results (elevated serum transaminases)

Skin and subcutaneous tissue disorders

  • skin rash

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

Cardiac disorders(at high doses during prolonged treatment)

  • palpitations
  • severe chest pain (symptoms of myocardial infarction or heart attack)
  • shortness of breath, difficulty breathing when lying down, swelling of feet and legs (signs of heart failure)

If these symptoms appear, consult your doctor immediately

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

Immune system disorders

  • swelling of face, eyes, or tongue, difficulty swallowing, wheezing, hives, and generalized itching, rash, fever, abdominal cramps, chest discomfort, difficulty breathing, dizziness, loss of consciousness (severe allergic reaction)

If these symptoms appear, consult your doctor immediately

Nervous system disorders

  • drowsiness

Respiratory, thoracic, and mediastinal disorders

  • asthma

Gastrointestinal disorders

  • stomach pain
  • reflux
  • bloody diarrhea
  • gastric or intestinal ulcer with or without bleeding or perforation (vomiting blood and appearance of blood in stool).If these symptoms appear, consult your doctor immediately

Hepatobiliary disorders

  • liver function alteration
  • hepatitis with or without jaundice.If these symptoms appear, consult your doctor immediately

Skin and subcutaneous tissue disorders

  • hives

General disorders and administration site conditions

  • fluid retention, with swelling (edema)

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

Blood and lymphatic system disorders

  • signs of anemia, such as fatigue, headache, shortness of breath when exercising, dizziness, paleness (anemia), frequent infections with fever, chills, sore throat, or mouth ulcers (leucopenia), bleeding or bruising more easily than normal (thrombocytopenia)

If these symptoms appear, consult your doctor immediately

Immune system disorders

  • swelling of face

Psychiatric disorders

  • disorientation
  • depression
  • insomnia
  • nightmares
  • irritability
  • psychotic reactions

Nervous system disorders

  • tingling sensation
  • memory disorders
  • seizures
  • anxiety
  • tremors
  • meningitis (inflammation of the membranes surrounding the brain) with symptoms such as fever, nausea, vomiting, headache, neck stiffness, or extreme sensitivity to bright light.If these symptoms appear, consult your doctor immediately
  • gustatory disorders
  • cerebral infarction

Eye disorders

  • blurred vision
  • double vision

Vestibular disorders

  • tinnitus

Vascular disorders

  • hypertension (high blood pressure)
  • vasculitis (inflammation of blood vessel walls)

Respiratory, thoracic, and mediastinal disorders

  • difficulty breathing, wheezing (neumonitis)

If these symptoms appear, consult your doctor immediately

Gastrointestinal disorders

  • worsening of Crohn's disease and ulcerative colitis
  • constipation
  • swelling of the tongue (glossitis)
  • inflammation of the mucous membrane of the mouth (stomatitis)
  • difficulty swallowing (esophageal alteration)
  • intense pain in the upper abdomen, nausea, vomiting, and loss of appetite (signs of pancreatitis).If these symptoms appear, consult your doctor immediately

Skin and subcutaneous tissue disorders

  • severe skin reactions with rash, redness, blisters on lips, mouth, or eyes, skin peeling, accompanied by fatigue, nausea, loss of appetite, fever, chills, headache, cough, or body pain (Stevens-Johnson syndrome or toxic epidermal necrolysis).If these symptoms appear, consult your doctor immediately
  • generalized rash (eczema)
  • redness (erythema and erythema multiforme)
  • skin peeling (dermatitis exfoliativa)
  • hair loss
  • solar allergy (photosensitivity reaction)
  • bruising
  • itching

Renal and urinary disorders

  • renal function anomalies that cause swelling in feet or legs and sudden decrease in urine output (acute renal failure, interstitial nephritis, papillary necrotic renal)
  • blood in urine (hematuria)
  • foam in urine (nephrotic syndrome)

If these symptoms appear, consult your doctor immediately

Isolated cases

Hepatobiliary disorders

  • liver function anomalies that cause yellowing of skin and eyes, fever, upper abdominal pain, and bruising (hepatic insufficiency, fulminant hepatitis, hepatic necrosis).

If these symptoms appear, consult your doctor immediately

Reporting of adverse reactions:

If you experience any type of adverse reaction, consult your doctor or pharmacist, even if it is a possible adverse reaction that does not appear in this prospectus. You can also report them directly through the Spanish System for the Pharmacovigilance of Medicines for Human Use: http://www.notificaram.es. By reporting adverse reactions, you can contribute to providing more information on the safety of this medicine.

5. Conservation of Voltarén Retard 100 mg

Keep this medication out of the sight and reach of children.

Do not store at a temperature above30°C. Store the blister pack in the outer packaging to protect it from moisture.

Do not use this medication after the expiration date that appears on the packaging after CAD. The expiration date is the last day of the month indicated.

Medications should not be disposed of through drains or in the trash.Deposit the containers and medications you no longer need at the SIGRE collection pointat the pharmacy. If in doubt, please ask your pharmacist how to dispose of the containers and medications you no longer need. By doing so, you will help protect the environment.

6. Content of the packaging and additional information

Composition of voltaren retard

  • The active ingredient is diclofenac sodium. Each tablet contains 100 mg of diclofenac sodium.
  • The other components (excipients) are sucrose, cetyl alcohol, anhydrous colloidal silica (E-551), povidone (E-1201), magnesium stearate (E-470b), hypromellose (E-464), polisorbate 80, titanium dioxide (E-171), iron oxide red (E-172), talc (E-553b), and polyethylene glycol 8000 (E-1521).

Appearance of voltaren retard and content of the packaging

Modified-release round tablets, pink in color with "CG" on one side and "CGC" on the other, in Al/PVC/PE/PVDC blisters, in packs of 20 tablets.

Holder of the marketing authorization

Novartis Farmacéutica, S.A.

Gran Via de les Corts Catalanes, 764

08013 Barcelona – Spain

Responsible for manufacturing

Novartis Farma S.p.A.

Via Provinciale Schito, 131 (Torre Annunziata)

Naples – Italy

Novartis Farmacéutica, S.A.

Gran Via de les Corts Catalanes, 764

08013 Barcelona – Spain

Novartis Pharma GmbH

Roonstrasse 25

DE-90429 Nuremberg

Germany

Last review date of this leaflet: 11/2023

The detailed and updated information on this medication is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS) http://www.aemps.gob.es/

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Cetilico, alcohol (59 mg mg), Sacarosa (119 mg mg), Sacarosa (trazas mg mg)
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