Elements for a Public Summary. [Product Name] 40 mg/ml oral suspension. VI.2.1 Overview of disease epidemiology

Similar documents
Elements for a Public Summary

Etoricoxib STADA 30 mg, 60 mg, 90 mg and 120 mg film-coated tablets , Version V1.2 PUBLIC SUMMARY OF THE RISK MANAGEMENT PLAN

Package leaflet: Information for the user. Noxafil 40 mg/ml oral suspension posaconazole

Summary of the risk management plan (RMP) for Voriconazole Hospira (voriconazole)

Elements for a Public Summary

Voriconazole 200 mg powder for solution for infusion 03 Jun version 3.0 PUBLIC SUMMARY OF THE RISK MANAGEMENT PLAN

PUBLIC SUMMARY OF RISK MANAGEMENT PLAN VORICONAZOLE ORION 200 MG FILM-COATED TABLETS

VI.2 Elements for a Public Summary DULOXETINE Pharmalex 30 mg hard gastro-resistant capsules DULOXETINE Pharmalex 60 mg hard gastro-resistant capsules

RISK MANAGEMENT PLAN (RMP) PUBLIC SUMMARY ETORICOXIB ORION (ETORICOXIB) 30 MG, 60 MG, 90 MG & 120 MG FILM-COATED TABLET DATE: , VERSION 1.

Elements for a Public Summary. Overview of disease epidemiology

Itraconazole DIGICON. Composition: MOLECULAR INTRODUCTION

Elements for a Public Summary

Risk What is known Preventability Known hypersensitivity to macrolide antibiotic drugs or to any of its excipients.

VI.2 Elements for a public summary

PUBLIC SUMMARY OF RISK MANAGEMENT PLAN (RMP) CANDESARTAN/HYDROCHLOROTHIAZIDE ORION 8 MG/12.5 MG, 16 MG/12.5 MG, 32 MG/12.5 MG, 32 MG/25 MG ORION

Elements for a Public Summary

Voriconazole October 2015 Risk Management Plan. Voriconazole

Summary of the risk management plan (RMP) for Kyprolis (carfilzomib)

PUBLIC SUMMARY OF RISK MANAGEMENT PLAN (RMP) CIPROFLOXACIN ORION 750 MG FILM-COATED TABLETS ORION OYJ DATE: , VERSION 1.

Supplementary Appendix

Nocturnal polyuria has been linked to abnormalities of the daily rhythm of (circadian rhythmic) release of naturally occurring antidiuretic hormone.

Elements for a public summary

Eplerenon Medical Valley + Eplerenon Stada

Summary of the risk management plan (RMP) for Lenvima (lenvatinib)

London New Drugs Group APC/DTC Briefing

Summary of the risk management plan (RMP) for Ristempa (pegfilgrastim)

Package leaflet: Information for the patient Tranexamic acid 100 mg/ml Solution for Injection tranexamic acid

Risk Management Plan

Elements for a Public Summary

PUBLIC SUMMARY OF THE RISK MANAGEMENT PLAN

Elements for a Public Summary Overview of disease epidemiology

VI.2 Elements for a public summary

Elements for a public summary. VI.2.1 Overview of disease epidemiology

Summary of the Risk Management Plan (RMP) V. 1.6, July 2017 for BAVENCIO. Avelumab 200 mg/10 ml. Concentrate for Solution for Infusion

Summary of the risk management plan (RMP) for Portrazza (necitumumab)

Summary of the risk management plan (RMP) for Clopidogrel/Acetylsalicylic acid Teva (clopidogrel / acetylsalicylic acid)

Cigna Drug and Biologic Coverage Policy

Pregabalin Aristo Version: RMP-Pregabalin0

Summary of the risk management plan (RMP) for Cresemba (isavuconazole)

Mycamine Micafungin (as sodium)

Elements for a Public Summary

PART VI: SUMMARY OF THE RISK MANAGEMENT PLAN

Overview of disease epidemiology

Management of fungal infection

Summary of the risk management plan (RMP) for Zerbaxa (ceftolozane / tazobactam)

METHYLDOPA 250 mg Film-coated Tablets

Elements for a Public Summary

Hyperandrogenism and polycystic ovary syndrome are clear casual factors (trends) which result in hirsuitism and acne.

Risk Management Plan Summary

RABEPRAZOL 10mg and 20mg Gastro-resistant Tablets

Piazza G, Creager M. Thromboangiitis Obliterans. Circulation Apr 27; 121(16):

Flukonazol 50mg Capsules, 150mg Capsules

Important safety information to minimise the risk of immune-related adverse reactions

Summary of the risk management plan (RMP) for Neofordex (dexamethasone)

srmp Atorvastatin Medical Valley

Elements for a public summary

VI.2 Elements for a public summary. VI.2.1 Overview of disease epidemiology

PART III: CONSUMER INFORMATION. POSANOL (posaconazole)

Ezetimib Stada 10 mg tablets

PACKAGE LEAFLET: INFORMATION FOR THE USER. Fibrovein 3%, 1%, 0.5% and 0.2% Solution for Injection Sodium tetradecyl sulphate

Package leaflet: Information for the patient. Tranexamic Acid 100 mg/ml, Solution for Injection tranexamic acid

Part VI: Summary of the risk management plan by product

Antifungal Agents - Cresemba (isavuconazonium), Vfend. Prior Authorization Program Summary

Summary of the risk management plan (RMP) for Spectrila (asparaginase)

Part VI: Summary of the risk management plan by product

Epidemiology and ecology of fungal diseases

A study conducted in Norway found the combined estimate for panic and generalized anxiety disorder was 1.10 per 1,000 person-years.

EU-Risk Management Plan for Emtricitabine/Tenofovir (NL/H/3635/001/DC and NL/H/3636/001/DC) V1.3

Summary of the risk management plan (RMP) for Oncaspar (pegaspargase)

Summary of the risk management plan (RMP) for Budesonide/Formoterol Teva (budesonide / formoterol)

Elements for a Public Summary

Package leaflet: Information for the user. Cefixime ABR 100 mg/5 ml powder for oral suspension Cefixime

Elements for a Public Summary

Package leaflet: Information for the user Cyklokapron 500 mg Solution for Injection tranexamic acid

PATIENT INFORMATION LEAFLET

Vancomycin Orion , Version 2 Public Summary of the Risk Management Plan

Elements for a Public Summary

Bloodborne Pathogens. Introduction to Fungi. Next >> COURSE 2 MODULE 4

PATIENT INFORMATION LEAFLET POLLENTYME S AND TABS

Zerlinda (MRP DK/H/2265/001)

Summary of the risk management plan (RMP) for Vylaer Spiromax (budesonide / formoterol)

Elements for a Public Summary

PATIENT INFORMATION LEAFLET DYNARB RANGE

Annex I. Scientific conclusions and grounds for the variation to the terms of the Marketing Authorisation(s)

SYNACTHEN DEPOT i.m. tetracosactide hexaacetate

Elements for a Public Summary Overview of disease epidemiology

7.2 Part VI.2 Elements for a Public Summary

VI.2 Elements for a Public Summary

Summary of the risk management plan (RMP) for DuoResp Spiromax (budesonide / formoterol)

srmp DK/H/2377/ /DC Gliclazid Sigillata

Cabometyx 20/40/60 mg. Film-coated tablets. Elements for a Public Summary Summary of the Safety Risk Management Plan (RMP)

Discussing TECENTRIQ (atezolizumab) with your healthcare team

Elements for a public summary

Elements for a public summary

Summary of the risk management plan (RMP) for Kengrexal (cangrelor)

Pathogens with Intermediate Virulence Dermatophytes opportunistic Pathogens

Fungi are eukaryotic With rigid cell walls composed largely of chitin rather than peptidoglycan (a characteristic component of most bacterial cell

(sunitinib malate) for Kidney Cancer

INFORMATION FOR THE CONSUMER IMPORTANT INFORMATION YOU SHOULD KNOW ABOUT

Transcription:

VI.2 Elements for a Public Summary [Product Name] 40 mg/ml oral suspension VI.2.1 Overview of disease epidemiology Fungi (yeasts) are small organisms that feed by breaking down tissue. In humans, fungi typically attack skin, hair and nails. Fungal spores can be spread through human-to-human contact, but also through contact with infected animals, objects (e.g. towels) or soil. In general, elderly patients, those with supressed immune system, with type 1 diabetes, who are overweight and who have poor circulation are at a higher risk of fungal infections. Invasive aspergillosis STADA Arzneimittel AG Page 41 of 76

Aspergillosis is an infection caused by mold Aspergillus. The symptoms resulting from aspergillosis infection usually affect the breathing system (such as lungs). In some people, Aspergillus triggers an allergic reaction. The most serious form of aspergillosis, invasive aspergillosis, occurs when the infection spreads to blood vessels and to other body parts. Fusariosis Fusarioisis is caused by fungi of the Fusarium family and typically affects the skin. It is common in cancer patients who are immunocompromised due to anti-cancer medication. Chromoblastomycosis and mycetoma Mycetoma typically affects the skin; feet are the most common site of infection. It is typically chronic and may, in severe cases, result in amputation of the infected body part. It is typically found in India, Mexico, Saudi Arabia, Venezuela and Sub-Saharan Africa. Mycetoma is seen most frequently in men between the ages of 20 and 40 years and is found in farmers and workers in rural areas. Chromoblastomycosis is also a skin infection. It is usually chronic, slowly progressive and localised, most frequent in the foot. Crusted lesions typically appear at the infection site. It is more common in tropical regions (e.g. Madagascar). Coccidioidomycosis Also known as valley fever, coccidioidomycosis is caused by fungus Coccidioides, found in the soil in North and South America. The infection may cause fever, chest pain and coughing. Oropharyngeal candidiasis Candidiasis (thrush) is an infection caused by Candida species (most often Candida albicans). Symptoms include white spots in the mouth, redness in the mouth and taste loss / unpleasant feeling in the mouth. Candida species are the most common cause of fungal infections in the patients having an impaired immune system. Candidal infections are also one of the most common infections acquired in hospital. VI.2.2 Summary of treatment benefits [Product Νame] contains a medicine called posaconazole. This belongs to a group of medicines called antifungals. It is used to prevent and treat many different fungal infections. This medicine works by killing or stopping the growth of some types of fungi that can cause infections. [Product Νame] can be used in adults to treat the following types of fungal infections when other antifungal medicines have not worked or you have had to stop taking them: infections caused by fungi of the Aspergillus family that have not improved during treatment with the anti-fungal medicines amphotericin B or itraconazole or when these medicines have had to be stopped; infections caused by fungi of the Fusarium family that have not improved during treatment with amphotericin B or when amphotericin B has had to be stopped; infections caused by fungi that cause the conditions known as chromoblastomycosis and mycetoma that have not improved during treatment with itraconazole or when itraconazole has had to be stopped; infections caused by a fungus called Coccidioides that have not improved during treatment with one or more of amphotericin B, itraconazole or fluconazole or when these medicines have had to be stopped. Infections in the mouth or throat area (known as thrush ) caused by fungi called Candida, which were not previously treated. STADA Arzneimittel AG Page 42 of 76

This medicine can also be used to prevent fungal infections in adults who are at high risk of getting a fungal infection, such as: patients who have a weak immune system due to having chemotherapy for acute myelogenous leukemia (AML) or myelodysplastic syndromes (MDS) patients having high-dose immunosuppressive therapy after hematopoietic stem cell transplant (HSCT). VI.2.3 Unknowns relating to treatment benefits The safety and efficacy of posaconazole in children aged below 18 years have not been established. VI.2.4 Summary of safety concerns Important identified risks Risk What is known Preventability Liver problems Various liver problems may occur in patients treated with (Hepatic events elevated posaconazole. Elevated liver liver enzymes, hepatotoxicity, function tests were generally hepatic failure, hepatitis) reversible on discontinuation of therapy and in some instances these tests normalised without interruption of therapy. Rarely, more severe liver reactions have been reported. Posaconazole should be used with caution in patients with liver impairment due to limited clinical experience and the possibility that posaconazole plasma levels may be higher in these patients. Blood coagulation disorder and haemolytic uraemic syndrome (when red blood cells breakup, which may happen with or without kidney failure) (Blood - thrombotic thrombocytopenic purpura, haemolytic uraemic syndrome) Blood coagulation disorder (thrombotic thrombocytopenic purpura) and haemolytic uraemic syndrome (when red blood cells breakup, which may happen with or without kidney failure) may occur in up to 1 in 1000 patients treated with posaconazole. Your dcotor may need to perform liver function tests before and during therapy with posaconazole. The dose of posaconazole may need to be adjusted by your doctor based on these tests. Tell your doctor if you have or have ever had any blood problems. Inform your doctor if you notice any of the following symptoms: fatigue bruising urination problems abdominal pain and/or diarrhoea STADA Arzneimittel AG Page 43 of 76

Abnormal heart rhytm (Cardiac Torsades de pointes) Interactions with other drugs (General drug interaction) Torsades de pointes, an abnormal heart rhytm that can lead to serious heart problems, may occur when posaconazole is taken together with terfenadine, astemizole, cisapride, pimozide, halofantrine or quinidine. Multiple drug interactions are known for posaconazole. These may affect the level of posaconazole in your body and the effect it has on the treating disease. The risk of side effects may be increased in some cases. Tell your doctor if you are taking any other drigs at the same time as [Product Name]. [Product Name] should not be co-administered with terfenadine, astemizole, cisapride, pimozide, halofantrine or quinidine. Tell your doctor if you are taking any other drigs at the same time as [Product Name]. Your doctor may decide to adjust the dosage of [Product Name] or of other medicines so as to minimise the chance of adverse events. Important potential risks Risk Blood Agranulocytosis, aplastic anaemia Cardiac QTc prolongation, heart failure, myocardial infarction Psychiatric depression, suicide Endocrine adrenal insufficiency CNS convulsions, cerebral ischaemia, cerebral hemorrhage Respiratory pulmonary haemorrhage Vascular hypertension, venous thrombosis, arterial thrombosis What is known (Including reason why it is considered a potential risk) Patients treated with posaconazole may be at an increased risk of developing aplastic anaemia (deficiency in all blood cell types). No further data is available. No clinical data are available for the risk agranulocytosis. Various heart problems may occur with posaconazole therapy. Posaconazole therapy may lead to depression in up to 1 in 1000 patients treated with posaconazole. No further data is available. No clinical data are available for the risk suicide. Posaconazole therapy may lead to adrenal insufficiency (adrenal glands not producing adequate amounts of steroid hormones) in up to 1 in 1000 patients treated with posaconazole. No further data is available. Various central nervous system problems, such as seizures, may occur with posaconazole therapy. Patients treated with posaconazole may be at an increased risk of developing bleeding from the lung. No further data is available. Various vascular problems (high blood pressure) may occur with posaconazole therapy. STADA Arzneimittel AG Page 44 of 76

Metabolism hypokalaemia Visual photopsia, visual brightness, visual disturbances Neoplasms Occurrence of any neoplasm/malignancy, especially: Hepatic adenoma; Hepatic neoplasm; Adrenal adenoma; Adrenal neoplasm; Phaeochromocytoma Infections Fungal infections Low potassium levels may occur in up to 1 in 10 patients treated with posaconazole. Visual disturbances may occur with posaconazole therapy. No evidence of an increased risk of neoplasms in patients using posaconazole has been established. Patients who have severe diarrhoea or vomiting should be monitored closely for breakthrough fungal infections. Missing information Risk Experience in children What is known The safety and efficacy of posaconazole in children aged below 18 years have not been established VI.2.5 Summary of risk minimisation measures by safety concern All medicines have a Summary of Product Characteristics (SPC) which provides physicians, pharmacists and other health care professionals with details on how to use the medicine, the risks and recommendations for minimising them. An abbreviated version of this in lay language is provided in the form of the package leaflet (PL). The measures in these documents are known as routine risk minimisation measures. This medicine has no additional risk minimisation measures. VI.2.6 Planned post authorisation development plan No post-authorisation studies have been imposed or are planned. VI.2.7 Summary of changes to the Risk Management Plan over time Not applicable. STADA Arzneimittel AG Page 45 of 76