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Libertek is a brand name for Roflumilast. The medicine, its uses, side effects and dosage are the same regardless of brand.
Used for: Libertek is indicated for maintenance treatment of severe chronic obstructive pulmonary disease (COPD) (FEV1 post-bronchodilator less than 50% predicted) associated with chronic bronchitis in adult patients with a history of frequent exacerbations as add on to bronchodilator treatment.
Verbatim from this product's EMA label. Tap a section to expand.
Posology The recommended dose is 500 micrograms (one tablet) roflumilast once daily. 1). Libertek has been studied in clinical trials for up to one year. Special populations Elderly No dose adjustment is necessary. Renal impairment No dose adjustment is necessary.
3). Paediatric population There is no relevant use of Libertek in the paediatric population (under 18 years) in the indication COPD. Method of administration For oral use. The tablet should be swallowed with water and taken at the same time every day.
The tablet can be taken with or without food.
Summary of the safety profile In clinical COPD studies, approximately 16% of patients experienced adverse reactions with roflumilast (compared to 5% in placebo). 7%). The majority of these adverse reactions were mild or moderate. These adverse reactions mainly occurred within the first weeks of therapy and mostly resolved on continued treatment.
Tabulated list of adverse reactions Within the following table, adverse reactions are ranked under the MedDRA frequency classification: Very common (≥1/10); common (≥1/100 to <1/10); uncommon (≥1/1,000 to <1/100); rare (≥1/10,000 to <1/1,000); very rare (<1/10,000), not known (cannot be estimated from the available data).
Medicinal product no longer authorised 6 Table 1. Adverse reactions with roflumilast in clinical COPD studies and post-marketing experience Frequency System Organ Class Common Uncommon Rare Immune system disorders Hypersensitivity Angioedema Endocrine disorders Gynaecomastia Metabolism and nutrition disorders Weight decreased Decreased appetite Psychiatric disorders Insomnia Anxiety Suicidal ideation and behaviour* Depression Nervousness Panic attack Nervous system disorders Headache Tremor Vertigo Dizziness Dysgeusia Cardiac disorders Palpitations Respiratory, thoracic and mediastinal disorders Respiratory tract infections (excluding Pneumonia) Gastrointestinal disorders Diarrhoea Nausea Abdominal pain Gastritis Vomiting Gastro-esophageal reflux disease Dyspepsia Haematochezia Constipation Hepatobiliary disorders Gamma-GT increased Aspartate aminotransferase (AST) increased Skin and subcutaneous tissue disorders Rash Urticaria Musculoskeletal and connective tissue disorders Muscle spasms and weakness Myalgia Back pain Blood creatine phosphokinase (CPK) increased General disorders and administration site conditions Malaise Asthenia Fatigue Description of selected adverse reactions * In clinical studies and post-marketing experience, rare instances of suicidal ideation and behaviour, including suicide, were reported.
All patients should be informed about the risks of Libertek and the precautions for safe use and should be given a patient card before starting Libertek. Rescue medicinal products Libertek is not indicated as rescue medicinal product for the relief of acute bronchospasms.
Weight decrease In 1-year studies (M2-124, M2-125), a decrease of body weight occurred more frequently in patients treated with roflumilast compared to placebo-treated patients. After discontinuation of roflumilast, the majority of patients had regained body weight after 3 months.
Body weight of underweight patients should be checked at each visit. Patients should be advised to check their body weight on a regular basis. In the event of an unexplained and clinically concerning weight decrease, the intake of roflumilast should be stopped and body weight should be further followed-up.
g. : methotrexate, azathioprine, infliximab, etanercept, or oral corticosteroids to be taken long-term; except short-term systemic corticosteroids). Experience in patients with latent infections such as tuberculosis, viral hepatitis, herpes viral infection and herpes zoster is limited.
Patients with congestive heart failure (NYHA grades 3 and 4) have not been studied and therefore treatment of these patients is not recommended. Psychiatric disorders Roflumilast is associated with an increased risk of psychiatric disorders such as insomnia, anxiety, nervousness and depression.
8). The risks and benefits of starting or continuing treatment with roflumilast should be carefully assessed if patients report previous or existing psychiatric symptoms or if concomitant treatment with other medicinal products likely to cause psychiatric events is intended.
Roflumilast is not recommended in patients with a history of depression associated with suicidal ideation or behaviour. Patients and caregivers should be instructed to notify the prescriber of anyMedicinal product no longer authorised 4 changes in behaviour or mood and of any suicidal ideation.
1. Moderate or severe hepatic impairment (Child-Pugh B or C).
Not medical advice. Always read the patient information leaflet and follow your prescriber or pharmacist.
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4). 3%). 7%). 2% in patients with a baseline body weight ≥60 kg, treated with roflumilast when compared to those treated with placebo. Concomitant treatment with long acting muscarinic antagonists (LAMA) A higher incidence of weight decrease, decreased appetite, headache and depression was observed during Study RO-2455-404-RD in patients receiving concomitant roflumilast and long-acting muscarinic antagonists (LAMA) plus concomitant inhaled corticosteroids (ICS) and long acting B2 agonists (LABA) compared to those treated only with concomitant roflumilast, ICS and LABA.
3%). Reporting of suspected adverse reactions Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the national reporting system listed in Appendix V.
If patients suffered from new or worsening psychiatric symptoms, or suicidal ideation or suicidal attempt is identified, it is recommended to discontinue treatment with roflumilast. Persistent intolerability While adverse reactions like diarrhoea, nausea, abdominal pain and headache mainly occur within the first weeks of therapy and mostly resolve on continued treatment, roflumilast treatment should be reassessed in case of persistent intolerability.
5). 8). Theophylline There are no clinical data to support the concomitant treatment with theophylline for maintenance therapy. Therefore, the concomitant treatment with theophylline is not recommended. Lactose Libertek tablets contain lactose.
Patients with rare hereditary problems of galactose intolerance, the Lapp lactase deficiency or glucose-galactose malabsorption should not take this medicinal product.