Quest for the right Drug
ז'בלור JAVLOR (VINFLUNINE DITARTRATE)
תרופה במרשם
תרופה בסל
נרקוטיקה
ציטוטוקסיקה
צורת מתן:
תוך-ורידי : I.V
צורת מינון:
תרכיז להכנת תמיסה לאינפוזיה : CONCENTRATE FOR SOLUTION FOR INFUSION
עלון לרופא
מינוניםPosology התוויות
Indications תופעות לוואי
Adverse reactions התוויות נגד
Contraindications אינטראקציות
Interactions מינון יתר
Overdose הריון/הנקה
Pregnancy & Lactation אוכלוסיות מיוחדות
Special populations תכונות פרמקולוגיות
Pharmacological properties מידע רוקחי
Pharmaceutical particulars אזהרת שימוש
Special Warning עלון לרופא
Physicians Leaflet
Adverse reactions : תופעות לוואי
4.8 Undesirable effects Summary of the safety profile The most frequent treatment-related adverse reactions reported in the two phase II and one phase III trials in patients with transitional cell carcinoma of the urothelium (450 patients treated with vinflunine) were haematological disorders, mainly neutropenia and anaemia; gastrointestinal disorders, especially constipation, anorexia, nausea, stomatitis/mucositis, vomiting, abdominal pain and diarrhoea and general disorders such as asthenia/fatigue. Tabulated list of adverse reactions Adverse reactions are listed below by System Organ Class, frequency and grade of severity (NCI CTC version 2.0). Frequency of adverse reactions is defined using the following convention: 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 available data). Within each frequency grouping, adverse reactions are presented in order of decreasing seriousness. Table 4 Adverse reactions observed in patients with transitional cell carcinoma of the urothelium treated with vinflunine System Organ Class Frequency Adverse Reactions Worst NCI Grade per patient (%) All grades Grade 3-4 Infections and infestations Common Neutropenic infection 2.4 2.4 Infections (viral, bacterial, 7.6 3.6 fungal) Uncommon Neutropenic sepsis 0.2 0.2 Neoplasm benign, Uncommon Tumor pain 0.2 0.2 malignant and unspecified Blood and lymphatic Very common Neutropenia 79.6 54.6 system disorders Leucopenia 84.5 45.2 Anaemia 92.8 17.3 Thrombocytopenia 53.5 4.9 Common Febrile neutropenia 6.7 6.7 Immune system disorders Common Hypersensitivity 1.3 0.2 Endocrine disorders Uncommon Syndrome of Inappropriate Antidiuretic Hormone 0.4 b 0.4 b Secretion (SIADH) a Metabolism and nutrition Very common Hyponatraemia 39.8 11.7 disorders Decreased appetite 34.2 2.7 Common Dehydration 4.4 2.0 Psychiatric disorders Common Insomnia 5.1 0.2 Nervous system disorders Very Peripheral sensory 11.3 0.9 Common neuropathy Common Syncope 1.1 1.1 Headache 6.2 0.7 Dizziness 5.3 0.4 Neuralgia 4.4 0.4 Dysgeusia 3.3 0 Neuropathy 1.3 0 Uncommon Peripheral motor neuropathy 0.4 0 Rare Posterior Reversible 0.03b 0.03b Encephalopathy Syndromea Eye disorders Uncommon Visual disturbance 0.4 0 Ear and Labyrinth Common Ear pain 1.1 0 disorders Uncommon Vertigo 0.9 0.4 Tinnitus 0.9 0 Cardiac disorders Common Tachycardia 1.8 0.2 Uncommon Myocardial ischaemia 0.7 0.7 Myocardial infarction 0.2 0.2 Vascular disorders Common Hypertension 3.1 1.6 Vein thrombosis 3.6 0.4 Phlebitis 2.4 0 Hypotension 1.1 0.2 Respiratory, thoracic and Common Dyspnoea 4.2 0.4 mediastinal disorders Cough 2.2 0 Uncommon Acute respiratory distress 0.2 0.2 syndrome Pharyngolaryngeal pain 0.9 0 Gastrointestinal disorders Very common Constipation 54.9 15.1 Abdominal pain 21.6 4.7 Vomiting 27.3 2.9 Nausea 40.9 2.9 Stomatitis 27.1 2.7 Diarrhoea 12.9 0.9 Common Ileus 2.7 2.2 Dysphagia 2.0 0.4 Buccal disorders 4.0 0.2 Dyspepsia 5.1 0.2 Uncommon Odynophagia 0.4 0.2 Gastric disorders 0.8 0 Oesophagitis 0.4 0.2 Gingival disorders 0.7 0 Skin and subcutaneous Very common Alopecia 28.9 NA tissue disorders Common Rash 1.8 0 Urticaria 1.1 0 Pruritus 1.1 0 Hyperhidrosis 1.1 0 Uncommon Dry skin 0.9 0 Erythema 0.4 0 Musculoskeletal and Very common Myalgia 16.7 3.1 connective tissue Common Muscular weakness 1.8 0.7 disorders Arthralgia 7.1 0.4 Back pain 4.9 0.4 Pain in jaw 5.6 0 Pain in extremity 2.4 0 Bone pain 2.9 0 Musculoskeletal pain 2.7 0.2 Renal and urinary Uncommon Renal failure 0.2 0.2 disorders General disorders and Very common Asthenia/Fatigue 55.3 15.8 administration site Injection site reaction 26.4 0.4 conditions Pyrexia 11.7 0.4 Common Chest pain 4.7 0.9 Chills 2.2 0.2 Pain 3.1 0.2 Oedema 1.1 0 Uncommon Extravasation 0.7 0 Investigations Very common Weight decreased 24.0 0.4 Uncommon Transaminases increased 0.4 0 Weight increased 0.2 0 a adverse reactions reported from post-marketing experience b frequency calculated on the basis of non-TCCU clinical trial Adverse reactions in all indications Adverse reactions occurring in patients with transitional cell carcinoma of the urothelium and in patients with other disease than this indication and potentially severe or adverse reactions that are a class effect of the vinca alkaloids are described below: Blood and lymphatic system disorders Grade 3/4 neutropenia was observed in 43.8% of patients. Severe anaemia and thrombocytopenia were less common (respectively 8.8 and 3.1%). Febrile neutropenia defined as ANC < 1,000/mm3and fever ≥ 38.5°C of unknown origin without clinically microbiologically documented infection (NCI CTC version 2.0) was observed in 5.2% of patients. Infection with Grade 3/4 neutropenia was observed in 2.8% of patients. Overall 8 patients (0.6% of the treated population) died from infection as a complication occurring during neutropenia. Gastrointestinal disorders Constipation is a class effect of the vinca alkaloids: 11.8% of patients experienced severe constipation during treatment with vinflunine. Grade 3/4 ileus reported in 1.9% of patients was reversible when managed by medical care. Constipation is managed by medical care (see section 4.4). Nervous system disorders Sensory peripheral neuropathy is a class effect of the vinca alkaloids. Grade 3 was experienced by 0.6% patients. All resolved during the study. Rare cases of Posterior Reversible Encephalopathy Syndrome have been reported (see section 4.4). Cardiovascular disorders Cardiac effects are a known class effect of the vinca alkaloids. Myocardial infarction or ischaemia were experienced by 0.5% of the patients and most of them had a pre-existing cardiovascular disease or risk factors. One patient died after myocardial infarction and another one due to a cardiopulmonary arrest. Few QT interval prolongations have been observed after the administration of vinflunine. Respiratory, thoracic and mediastinal disorders Dyspnoea occurred in 3.2% of the patients but was rarely severe (Grade 3/4: 1.2%). Bronchospam was reported in one patient treated with vinflunine for a different setting from the indication. 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. Any suspected adverse events should be reported to the Ministry of Health according to the National Regulation by using an online form (http://forms.gov.il/globaldata/getsequence/getsequence.aspx?formType=AdversEffectM edic@moh.health.gov.il ) or by email (adr@MOH.HEALTH.GOV.IL ).
שימוש לפי פנקס קופ''ח כללית 1994
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