Dacortin 30 mg comprimidos

Dacortín 30 mg tablets

Prednisone

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

-Keep this leaflet, as you may need to read it again.

-If you have any questions, consult your doctor or pharmacist.

-This medicine has been prescribed for you only. Do not give it to others, even if they have the same symptoms as you, as it may harm them.

-If you experience any side effects, consult your doctor or pharmacist, even if they are not listed in this leaflet.See section 4.

1. What Dacortín 30 mg is and what it is used for

2. What you need to know before you start taking Dacortín 30 mg

3. How to take Dacortín 30 mg

4. Possible side effects

5. Storage of Dacortín 30 mg

6. Contents of the pack and additional information

The prednisone contained in Dacortín 30 mg is a corticosteroid (glucocorticoid).

Dacortín 30 mg is used for the treatment of substitution in adrenal insufficiency including among others Addison's disease.

Due to its anti-inflammatory and immunosuppressive action, Dacortín 30 mg is used in the treatment of:

• rheumatic diseases, such as rheumatoid arthritis
• autoimmune diseases of collagen and blood vessels, such as systemic lupus erythematosus
• bronchial and pulmonary diseases such as asthma
• skin diseases, such as acute and severe urticaria and pemphigus
• blood diseases, such as acquired hemolytic anemia, thrombocytopenic purpura and others with tumor involvement, such as leukemia
• along with chemotherapy or radiation therapy
• gastrointestinal diseases, such as ulcerative colitis and Crohn's disease
• liver diseases, such as chronic active autoimmune hepatitis
• kidney diseases, such as nephrotic syndrome
• some inflammatory eye diseases, such as allergic conjunctivitis, keratitis, optic neuritis among others.

Do not take Dacortín 30 mg tablets:

• if you are allergic to prednisone, other glucocorticoids, or any of the other components of this medication (listed in section 6)
• if you have a stomach ulcer, gastritis, esophagitis (digestive system diseases)
• if you have viral infections (such as herpes simplex eye infection, chickenpox), before or after receiving a vaccine

Your doctor may have recommended taking Dacortín despite having one of the following conditions and requiring regular monitoring:

• if you have osteomalacia and osteoporosis (bone diseases)
• if you have severe diabetes
• if you have uncontrolled psychosis (mental disorder)
• if you have untreated tuberculosis
• if you have bacterial, fungal, amoebic, or systemic fungal infections
• if you have lymphomas (a type of lymphatic system tumor) that appeared after a tuberculosis vaccination
• if you have any psychiatric disorder. Consult your doctor about the suitability of using this medication
• if you have severe high blood pressure

• if you have asystole (heart disease) with pulmonary edema and uremia (a syndrome characterized by an excess of nitrogenous substances in the blood)
• if you have severe myasthenia (muscular disease)

• if you have renal insufficiency

Warnings and precautions

Consult your doctor or pharmacist before starting to take Dacortín 30 mg.

Treatment with Dacortín 30 mg may increase the risk of infections as it may decrease your body's defenses, leading to new infections or reactivating existing ones (e.g., tuberculosis or hepatitis B). In severe infections or in the case of tuberculosis, Dacortín should only be used in conjunction with treatment for the infection.

Inform your doctor if you experience any type of infection and if you have been vaccinated or plan to be vaccinated. If symptoms of acute diseases such as infectious diseases, digestive disorders, or mental alterations appear during treatment, consult your doctor.

Avoid contact with people who have chickenpox or measles. If you are exposed to these infections during treatment with Dacortín, contact a doctor immediately, even if you do not show any symptoms.

This medication should be administered with caution in people with stomach ulcers, ulcerative colitis (intestinal disease), diverticulitis (intestinal disease), or anastomosis (after surgery) or mental disorders.

If you have osteoporosis, your doctor may recommend taking additional calcium and vitamin D.

Inform your doctor if you have any heart disease and require high doses of prednisone.

If you are diabetic, or have heart failure and very high blood pressure or glaucoma, your doctor will perform regular checks.

If you are taking fluoroquinolones (e.g., ciprofloxacin), the risk of tendon ruptures and tendinitis increases.

Your doctor may increase the dose if you experience any stressful situation (infections, surgery, trauma, etc.).

In long-term treatments, your doctor will perform regular checks to prevent complications in the eyes, blood tests, growth control (in children and adolescents), and will monitor your hypothalamic-pituitary-adrenal axis function.

Contact your doctor if you experience blurred vision or other visual disturbances.

In prolonged treatments with Dacortín, your doctor may prescribe potassium supplements and reduce your sodium (salt) intake.

Consult your doctor before starting to take Dacortín if you have scleroderma (also known as systemic sclerosis, an autoimmune disorder), as daily doses of 15 mg or more may increase the risk of a severe complication called scleroderma renal crisis. Signs of scleroderma renal crisis include high blood pressure and decreased urine production. Your doctor may advise you to monitor your blood pressure and urine production regularly.

Careful consideration should be given to administering Dacortín to children, and if administered, it should be an intermittent or alternating treatment.

When administered to elderly patients, your doctor will monitor the patient regularly. Elderly patients should avoid long-term treatment with this medication.

Taking Dacortín may produce false results in skin tests for allergy tests (tuberculin test, allergy patches, etc.).

Use in athletes

This medication contains prednisone, which may produce a positive result in doping control tests.

Treatment should not be stopped abruptly but rather tapered off gradually. Do not stop taking this medication without consulting your doctor (see section 3 "How to take Dacortín").

Taking Dacortín 30 mg with other medications

Inform your doctor if you are taking or have recently taken other medications, including those purchased without a prescription.

Some medications may increase the effects of Dacortín, so your doctor will perform thorough checks if you are taking these medications (including some for HIV: ritonavir, cobicistat).

Dacortín may interact with the following medications:

• Nonsteroidal anti-inflammatory drugs (e.g., indomethacin, salicylates)
• Antidiabetic medications
• Enzyme inducers:
• • carbamazepine, phenytoin, phenobarbital, or primidone (medications used to treat epilepsy)
  • rifampicin, rifabutin (antibiotics)
• Enzyme inhibitors such as ketoconazole (used to treat fungal infections)
• ephedrine
• oral anticoagulants (e.g., Sintrom)
• estrogens (medications used to treat hormonal imbalances), oral contraceptives
• atropine
• cardiac glycosides (medications used to treat heart disease)
• diuretics that eliminate potassium (medications used to eliminate water) and laxatives
• praziquantel (antiparasitic medication)
• some medications used to treat high blood pressure
• some medications used to treat malaria
• immunosuppressive substances (medications used to prevent rejection)
• non-depolarizing neuromuscular blockers (medications used mainly in ICUs or operating rooms)
• growth hormone
• protirelin (medication that stimulates the thyroid)
• fluoroquinolones: may increase the risk of tendon damage.
• antacids
• salicylates (medications like aspirin)

Interference with laboratory tests: allergy tests may be suppressed.

Pregnancy and breastfeeding

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

Dacortín, like most medications, should not be administered during pregnancy or breastfeeding, unless your doctor considers it essential. You should inform your doctor as soon as possible if you become pregnant during treatment.

Dacortín passes into breast milk, so it is recommended to avoid breastfeeding during treatment, especially in long-term treatments and when high doses are used.

Driving and operating machinery

It should be noted that in long-term treatments, visual acuity may decrease. This may negatively affect your ability to drive and operate machinery.

Dacortín 30 mg contains lactose

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

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

As a general rule, the daily dose should be divided into several doses after meals and at bedtime. In some cases, it may be taken as a single dose in the morning, every day or on alternate days, with sufficient liquid.

As soon as a satisfactory response is obtained, you should take the general maintenance dose. Both doses will be determined by your doctor.

The dose depends on the type and severity of the disease and the individual response of the patient, and in prolonged treatments, the maintenance dose should be as low as possible.

The initial dose will be 20 to 90 mg per day in adults and 0.5 to 2 mg per day per kg of body weight in children.

The general maintenance dose will be 5 to 10 mg per day in adults and 0.25 to 0.5 mg per day per kg of body weight in children. When used in children as an anti-inflammatory and immunosuppressant, doses of 0.05 to 2 mg per day per kg of body weight are recommended.

To discontinue treatment, your doctor will indicate how to do it. For long treatments, a gradual reduction will be made: in general, the dose should be reduced by 10% every 8-15 days. For short treatments (less than 10 days), it is not necessary to make a gradual reduction in the dose.

In the elderly, the same posology as in adults will be applied, taking into account the recommendations mentioned in section 2 "Warnings and precautions".

If you take more Dacortín 30 mg than you should

In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicological Information Service, phone 91 562 0420, indicating the medication and the amount ingested.

If you forgot to take Dacortín 30 mg

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

If you interrupt the treatment with Dacortín 30 mg

Do not stop using this medication without consulting your doctor.

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

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

The observed side effects are, according to their frequency of presentation: very frequent (may affect more than 1 in 10 patients); frequent (may affect up to 1 in 10 patients); infrequent (may affect up to 1 in 100 patients); rare (may affect up to 1 in 1,000 patients); very rare (may affect up to 1 in 10,000 patients); unknown frequency (cannot be estimated from available data).

Most of the time, adverse reactions occur especially when used at high doses and in long treatments, and are detailed below:

Blood and lymphatic system disorders:leucocytosis (increase in white blood cells in the blood), lymphopenia (decrease in lymphocytes in the blood), eosinopenia (decrease in eosinophils in the blood), polycythemia (increase in red blood cells in the blood).

Endocrine disorders:signs of hyperadrenal activity (Cushing's syndrome, a disease caused by the increase in production of a hormone called cortisol); in prolonged treatments, adrenocortical insufficiency (a disease characterized by weakness, feeling of fatigue all the time, loss of appetite and weight).

Eye disorders:glaucoma and cataracts. Blurred vision.

Gastrointestinal disorders:gastric ulcer, intestinal bleeding, pancreatitis (inflammation of the pancreas).

General disorders and administration site conditions:delayed wound healing.

Immune system disorders:severe allergic reactions, including arrhythmias, bronchospasm, decrease or increase in blood pressure, circulatory insufficiency, heart attack.

Infections and infestations: lexisting infections may worsen and new infections may appear that are difficult to diagnose.

Metabolism and nutrition disorders: retention of fluids (edema), loss of potassium (which may cause alterations in heart rhythm), weight gain, increase in blood sugar, diabetes mellitus, increase in blood cholesterol and triglycerides, increase in appetite, delayed growth in children.

Cardiac disorders (unknown frequency):decreased heart rate.

Musculoskeletal and connective tissue disorders:muscle diseases and muscle weakness, tendon alterations, tendinitis, tendon ruptures, loss of calcium in bones, osteoporosis, delayed growth in children.

Nervous system disorders:increased intracranial pressure (especially in children), increased spasms in epileptic patients or appearance of epilepsy.

Psychiatric disorders:psychosis, mania, depression, hallucinations, emotional instability, irritability, increased activity, euphoria, anxiety, sleep disturbances, suicidal thoughts.

Reproductive and breast disorders: menstruation irregularities or absence of menstruation, hirsutism (excessive hair growth).

Skin and subcutaneous tissue disorders: acné or other skin problems (allergy, bruises, striae), edemas, changes in skin color, dermatitis around the mouth.

Vascular disorders:high blood pressure, increased risk of arteriosclerosis (narrowing and hardening of the arteries) and thrombosis (formation of blood clots), vasculitis, capillary fragility.

Renal and urinary disorders: crisis renal esclerodérmica in patients who already have scleroderma (an autoimmune disorder). The signs of a renal crisis are increased blood pressure and decreased urine production.

Reducing the dose rapidly after a long treatment may cause muscle and joint pain.

If you consider that any of the side effects you are experiencing is severe or if you notice any side effect not mentioned in this leaflet, inform your doctor or pharmacist.

Reporting of side effects:

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

No special storage conditions are required.

Keep Dacortín 30 mg tablets out of sight and reach of children.

Do not use Dacortín 30 mg tablets after the expiration date shown on the packaging after CAD. The expiration date is the last day of the month indicated.

Medicines should not be disposed of through drains or in the trash. Dispose of the packaging and unused medicines at the SIGRE collection point at the pharmacy. If in doubt, ask your pharmacist how to dispose of the packaging and unused medicines. By doing so, you will help protect the environment.

Composition of Dacortín 30 mg

• The active ingredient is prednisone. Each tablet contains30mg of prednisone.
• The other components are lactose monohydrate, cornstarch, povidone, carboxymethylcellulose sodium, talc, magnesium stearate, and purified water.

Appearance of the product and contents of the packaging

Dacortín 30 mg is presented in the form of white, oblong tablets. The upper face has a transverse groove with the number “15” engraved on either side of the groove. The lower face contains two grooves that divide the tablet into three parts; each part has the number “10” engraved on it. The tablet can be divided into 2 or 3 equal parts.

Dacortín 30 mg is presented in packaging of 30 or 500 tablets in blister packs.

Holder of the marketing authorization

Laboratorios ERN, S.A.

Perú, 228

08020 Barcelona, Spain

Responsible for manufacturing

Merck, S.L.

Merck Industrial Estate

08100 Mollet del Vallés (Barcelona), Spain

or

CYNDEA PHARMA, S.L.

Emiliano Revilla Sanz Industrial Estate

Avenida de Ágreda, 31 - 42110 Ólvega (Soria)

or

LABORATORIOS ERN, S.A.

Gorgs Lladó, 188

08210 Barberá del Vallés, Barcelona. Spain

Last review date of this leaflet: 09/2017

For detailed and updated information on this medication, please visit the website of the Spanish Agency for Medicines and Medical Devices (AEMPS)http://www.aemps.gob.es/.