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סלספט 500 מ"ג CELLCEPT 500 MG (MYCOPHENOLATE MOFETIL)
תרופה במרשם
תרופה בסל
נרקוטיקה
ציטוטוקסיקה
צורת מתן:
פומי : PER OS
צורת מינון:
טבליות מצופות פילם : FILM COATED TABLETS
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 Diarrhoea (up to 52.6%), leukopenia (up to 45.8%), bacterial infections (up to 39.9%) and vomiting (up to 39.1%) were among the most common and/or serious adverse reactions associated with the administration of CellCept in combination with ciclosporin and corticosteroids. There is also evidence of a higher frequency of certain types of infections (see section 4.4). Tabulated list of adverse reactions The adverse reactions from clinical trials and post-marketing experience are listed in Table 1, by MedDRA system organ class (SOC) along with their frequencies. The corresponding frequency category for each adverse reaction is based on 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) and very rare (<1/10,000). Due to the large differences observed in the frequency of certain adverse reactions across the different transplant indications, the frequency is presented separately for renal, hepatic and cardiac transplant patients. Table 1 Adverse reactions Adverse reaction (MedDRA) Renal Hepatic Cardiac transplant transplant transplant System Organ Class Frequency Frequency Frequency Infections and infestations Bacterial infections Very Common Very Common Very Common Fungal infections Common Very Common Very Common Protozoal infections Uncommon Uncommon Uncommon Viral infections Very Common Very Common Very Common Neoplasms benign, malignant and unspecified (including cysts and polyps) Benign neoplasm of skin Common Common Common Lymphoma Uncommon Uncommon Uncommon Lymphoproliferative disorder Uncommon Uncommon Uncommon Neoplasm Common Common Common Skin cancer Common Uncommon Common Blood and lymphatic system disorders Anemia Very Common Very Common Very Common Aplasia pure red cell Uncommon Uncommon Uncommon Bone marrow failure Uncommon Uncommon Uncommon Ecchymosis Common Common Very Common Leukocytosis Common Very Common Very Common Leukopenia Very Common Very Common Very Common Pancytopenia Common Common Uncommon Pseudolymphoma Uncommon Uncommon Common Thrombocytopenia Common Very Common Very Common Metabolism and nutrition disorders Acidosis Common Common Very Common Hypercholesterolemia Very Common Common Very Common Hyperglycemia Common Very Common Very Common Hyperkalemia Common Very Common Very Common Hyperlipidemia Common Common Very Common Hypocalcemia Common Very Common Common Hypokalemia Common Very Common Very Common Hypomagnesemia Common Very Common Very Common Hypophosphatemia Very Common Very Common Common Hyperuricaemia Common Common Very Common Gout Common Common Very Common Weight decreased Common Common Common Psychiatric disorders Confusional state Common Very Common Very Common Depression Common Very Common Very Common Insomnia Common Very Common Very Common Agitation Uncommon Common Very Common Anxiety Common Very Common Very Common Thinking abnormal Uncommon Common Common Nervous system disorders Dizziness Common Very Common Very Common Headache Very Common Very Common Very Common Hypertonia Common Common Very Common Paresthesia Common Very Common Very Common Somnolence Common Common Very Common Tremor Common Very Common Very Common Convulsion Common Common Common Dysgeusia Uncommon Uncommon Common Cardiac disorders Tachycardia Common Very Common Very Common Vascular disorders Hypertension Very Common Very Common Very Common Hypotension Common Very Common Very Common Lymphocele Uncommon Uncommon Uncommon Venous thrombosis Common Common Common Vasodilatation Common Common Very Common Respiratory, thoracic and mediastinal disorders Bronchiectasis Uncommon Uncommon Uncommon Cough Very Common Very Common Very Common Dyspnea Very Common Very Common Very Common Interstitial lung disease Uncommon Very Rare Very Rare Pleural effusion Common Very Common Very Common Pulmonary fibrosis Very Rare Uncommon Uncommon Gastrointestinal disorders Abdominal distension Common Very Common Common Abdominal pain Very Common Very Common Very Common Colitis Common Common Common Constipation Very Common Very Common Very Common Decreased appetite Common Very Common Very Common Diarrhea Very Common Very Common Very Common Dyspepsia Very Common Very Common Very Common Esophagitis Common Common Common Eructation Uncommon Uncommon Common Flatulence Common Very Common Very Common Gastritis Common Common Common Gastrointestinal hemorrhage Common Common Common Gastrointestinal ulcer Common Common Common Gingival hyperplasia Common Common Common Ileus Common Common Common Mouth ulceration Common Common Common Nausea Very Common Very Common Very Common Pancreatitis Uncommon Common Uncommon Stomatitis Common Common Common Vomiting Very Common Very Common Very Common Immune system disorders Hypersenstivity Uncommon Common Common Hypogammaglobulinaemia Uncommon Very Rare Very Rare Hepatobiliary disorders Blood alkaline phosphatase increased Common Common Common Blood lactate dehydrogenase increased Common Uncommon Very Common Hepatic enzyme increased Common Very Common Very Common Hepatitis Common Very Common Uncommon Hyperbilirubinaemia Common Very Common Very Common Jaundice Uncommon Common Common Skin and subcutaneous tissue disorders Acne Common Common Very Common Alopecia Common Common Common Rash Common Very Common Very Common Skin hypertrophy Common Common Very Common Musculoskeletal and connective tissue disorders Arthralgia Common Common Very Common Muscular weakness Common Common Very Common Renal and urinary disorders Blood creatinine increased Common Very Common Very Common Blood urea increased Uncommon Very Common Very Common Hematuria Very Common Common Common Renal impairment Common Very Common Very Common General disorders and administration site conditions Asthenia Very Common Very Common Very Common Chills Common Very Common Very Common Oedema Very Common Very Common Very Common Hernia Common Very Common Very Common Malaise Common Common Common Pain Common Very Common Very Common Pyrexia Very Common Very Common Very Common De novo purine synthesis Uncommon Uncommon Uncommon inhibitors associated acute inflammatory syndrome Description of selected adverse reactions Malignancies Patients receiving immunosuppressive regimens involving combinations of medicinal products, including CellCept, are at increased risk of developing lymphomas and other malignancies, particularly of the skin (see section 4.4). Three-year safety data in renal and cardiac transplant patients did not reveal any unexpected changes in incidence of malignancy compared to the 1-year data. Hepatic transplant patients were followed for at least 1 year, but less than 3 years. Infections All patients treated with immunosuppressants are at increased risk of bacterial, viral and fungal infections (some of which may lead to a fatal outcome), including those caused by opportunistic agents and latent viral reactivation. The risk increases with total immunosuppressive load (see section 4.4). The most serious infections were sepsis, peritonitis, meningitis, endocarditis, tuberculosis and atypical mycobacterial infection. The most common opportunistic infections in patients receiving CellCept (2 g or 3 g daily) with other immunosuppressants in controlled clinical trials in renal, cardiac and hepatic transplant patients followed for at least 1 year were candida mucocutaneous, CMV viraemia/syndrome and Herpes simplex. The proportion of patients with CMV viraemia/syndrome was 13.5%. Cases of BK virus associated nephropathy, as well as cases of JC virus associated progressive multifocal leukoencephalopathy (PML), have been reported in patients treated with immunosuppressants, including CellCept. Blood and lymphatic disorders Cytopenias, including leukopenia, anemia, thrombocytopenia and pancytopenia, are known risks associated with mycophenolate mofetil and may lead or contribute to the occurrence of infections and hemorrhages (see section 4.4). Agranulocytosis and neutropenia have been reported; therefore, regular monitoring of patients taking CellCept is advised (see section 4.4). There have been reports of aplastic anaemia and bone marrow failure in patients treated with CellCept, some of which have been fatal. Cases of pure red cell aplasia (PRCA) have been reported in patients treated with CellCept (see section 4.4). Isolated cases of abnormal neutrophil morphology, including the acquired Pelger-Huet anomaly, have been observed in patients treated with CellCept. These changes are not associated with impaired neutrophil function. These changes may suggest a ‘left shift’ in the maturity of neutrophils in haematological investigations, which may be mistakenly interpreted as a sign of infection in immunosuppressed patients such as those that receive CellCept. Gastrointestinal disorders The most serious gastrointestinal disorders were ulceration and hemorrhage which are known risks associated with mycophenolate mofetil. Mouth, esophageal, gastric, duodenal, and intestinal ulcers often complicated by hemorrhage, as well as hematemesis, melena, and hemorrhagic forms of gastritis and colitis were commonly reported during the pivotal clinical trials. The most common gastrointestinal disorders, however, were diarrhoea, nausea and vomiting. Endoscopic investigation of patients with CellCept-related diarrhoea have revealed isolated cases of intestinal villous atrophy (see section 4.4). Hypersensitivity Hypersensitivity reactions, including angioneurotic oedema and anaphylactic reaction, have been reported. Pregnancy, puerperium and perinatal conditions Cases of spontaneous abortion have been reported in patients exposed to mycophenolate mofetil, mainly in the first trimester, see section 4.6. Congenital disorders Congenital malformations have been observed post-marketing in children of patients exposed to CellCept in combination with other immunosuppressants, see section 4.6. Respiratory, thoracic and mediastinal disorders There have been isolated reports of interstitial lung disease and pulmonary fibrosis in patients treated with CellCept in combination with other immunosuppressants, some of which have been fatal. There have also been reports of bronchiectasis in children and adults. Immune system disorders Hypogammaglobulinaemia has been reported in patients receiving CellCept in combination with other immunosuppressants. General disorders and administration site conditions Oedema, including peripheral, face and scrotal oedema, was reported very commonly during the pivotal trials. Musculoskeletal pain such as myalgia, and neck and back pain were also very commonly reported. De novo purine synthesis inhibitors associated acute inflammatory syndrome has been described from post-marketing experience as a paradoxical proinflammatory reaction associated with mycophenolate mofetil and mycophenolic acid, characterised by fever, arthralgia, arthritis, muscle pain and elevated inflammatory markers. Literature case reports showed rapid improvement following discontinuation of the medicinal product. Special populations Paediatric population The type and frequency of adverse reactions in a clinical study, which recruited 92 paediatric patients aged 2 to 18 years who were given 600 mg/m2 mycophenolate mofetil orally twice daily, were generally similar to those observed in adult patients given 1 g CellCept twice daily. However, the following treatment-related adverse events were more frequent in the paediatric population, particularly in children under 6 years of age, when compared to adults: diarrhoea, sepsis, leucopenia, anaemia and infection. Elderly Elderly patients (≥ 65 years) may generally be at increased risk of adverse reactions due to immunosuppression. Elderly patients receiving CellCept as part of a combination immunosuppressive regimen may be at increased risk of certain infections (including cytomegalovirus tissue invasive disease) and possibly gastrointestinal haemorrhage and pulmonary oedema, compared to younger individuals. 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 /https://sideeffects.health.gov.il
פרטי מסגרת הכללה בסל
1. התרופה תינתן לטיפול במקרים האלה: א. מושתלי כליה. ב. מושתלי כבד ג. מושתלי לב. ד. מושתלי ריאה. ה. לופוס נפריטיס פעילה (מוכחת בביופסיה) בחולים לאחר כשלון טיפול בסטרואידים, בהם אין פגיעה במערכות חיוניות (כגון לב ומערכת העצבים המרכזית). 2. הטיפול בתרופה לגבי פסקת משנה 1(א) עד (ד) ייעשה לפי מרשם של רופא מומחה באימונולוגיה קלינית או רופא מומחה העוסק בתחום ההשתלות. (3) הטיפול בתרופה לגבי פסקת משנה 1(ה) ייעשה לפי מרשם של רופא מומחה בראומטולוגיה או רופא מומחה בנפרולוגיה.
מסגרת הכללה בסל
התוויות הכלולות במסגרת הסל
התוויה | תאריך הכללה | תחום קליני | Class Effect | מצב מחלה |
---|---|---|---|---|
לופוס נפריטיס פעילה (מוכחת בביופסיה) בחולים לאחר כשלון טיפול בסטרואידים, בהם אין פגיעה במערכות חיוניות (כגון לב ומערכת העצבים המרכזית). | ||||
מושתלי ריאה. | ||||
מושתלי לב | ||||
מושתלי כבד | ||||
מושתלי כליה |
שימוש לפי פנקס קופ''ח כללית 1994
לא צוין
תאריך הכללה מקורי בסל
09/03/1999
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סלספט 500 מ"ג