Quest for the right Drug
זומקטון 10 מ"ג ZOMACTON 10 MG (SOMATROPIN)
תרופה במרשם
תרופה בסל
נרקוטיקה
ציטוטוקסיקה
צורת מתן:
תת-עורי : S.C
צורת מינון:
אבקה וממס להכנת תמיסה להזרקה : POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
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 The subcutaneous administration of growth hormone may lead to loss or increase of adipose tissue as well as punctual haemorrhage and bruising at the injection site. System Organ Very Common Common Uncommon Rare Very rare Class (> 1/10) (>1/100, <1/10) (>1/100. <1/1,000) (>1/1,000, (<1/10,000) <1/10,000) Blood and anemia lymphatic system disorders Cardiac tachycardia, (adult) (children) disorders hypertension hypertension Ear and vertigo labyrinth disorders Endocrine hypothyroidism disorders Eye disorders papilloedema, diplopia Gastrointestinal vomiting, abdominal diarrhea disorders pain, flatulence, nausea General (adults) (children) weakness, injection disorders and oedema, (adults) oedema, site atrophy, injection administration peripheral (children) site hemorrhage, site conditions oedema peripheral injection site mass, oedema, hypertrophy injection site reactions, asthenia Immune system antibody disorders building Investigations renal function test abnormal Metabolism and (adult) mild (children) hypoglycemia, diabetes nutrition hyperglycemia glucose hyperphosphatemia mellitus type disorders tolerance II impaired Musculoskeletal (adults) (children) muscle atrophy, bone and connective arthralgia; arthralgia pain, carpal tunnel tissue disorders (adults) myalgia (children) syndrome myalgia (children) Stiffness in (adults) the extremities Stiffness in the extremities Neoplasms neoplasm malignant, (children) benign, neoplasm leukaemia malignant and unspecified Nervous system (adult) headache, somnolence, neuropathy, disorders headache, hypertonia, nystagmus intracranial (adult) (adult) insomnia pressure paresthesia increased, (children) insomnia, (children) paresthesia Psychiatric personality disorders disorders Renal and urinary incontinence, urinary disorders haematuria, polyuria, urine frequency/pollakiuria, urine abnormality Reproductive genital discharge, (children) system and breast (adult) gynecomastia gynecomastia disorders Skin and lipodystrophy, skin subcutaneous atrophy, dermatitis tissue disorders exfoliative, urticaria, hirsutism, skin hypertrophy Pancreatitis has been reported post-marketing during GH therapy (frequency unknown).Antibodies anti-somatropin: the protein somatropin may give rise to the formation of antibodies. Depending on the concerned product, these antibodies have been identified in a definite percentage of the treated population. Their binding capacity and their titers are generally low with no clinical consequence. However, testing for antibodies to somatropin should be performed in case of absence of response to somatropin therapy. Leukaemia: cases of leukaemia (very rare) have been reported in children with a GH deficiency, some of them being treated with somatropin and included in the post-marketing experience. However, there is no evidence of an increased risk of leukaemia without predisposition factors. Slipped capital femoral epiphysis and Legg-Calve-Perthes disease have been reported in children treated with GH. Slipped capital femoral epiphysis occurs more frequently in case of endocrine disorders and Legg-Calve-Perthes is more frequent in case of short stature. But, it is unknown if these 2 pathologies are more frequent or not while treated with somatropin. A discomfort, a pain in the hip and/or the knee must evocate their diagnosis. Other adverse drug reactions may be considered as class effect, as the hyperglycaemia due to the decrease in insulin-sensitivity, the decrease of free thyroxin level and the possible development of a benign intra-cranial hypertension. 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
א. התרופה האמורה תינתן לטיפול בכל אחד מאלה: (1) קומה נמוכה על רקע של כשל בהפרשה או הפרשה לא מתאימה של הורמון גדילה היפופיזרי (2) קומה נמוכה על רקע של תסמונת טרנר (3) קומה נמוכה עם אי ספיקה כליתית. ב. התרופה תינתן בהתאם לאישור ועדת ההיגוי לטיפול בהורמון גדילה של משרד הבריאות.
שימוש לפי פנקס קופ''ח כללית 1994
יירשם לפי אישור ועדת ההיגוי של משרד הבריאות
תאריך הכללה מקורי בסל
01/01/1995
הגבלות
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מידע נוסף