Quest for the right Drug
איסטוריסה 1 מ"ג ISTURISA 1 MG (OSILODROSTAT AS PHOSPHATE)
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 The most frequent adverse reactions reported in the pivotal phase III study with osilodrostat were adrenal insufficiency (51%), fatigue (44%), oedema (21%), vomiting (22%), nausea (42%) and headache (34%). The most serious adverse reaction associated with the use of osilodrostat is adrenal insufficiency (see also sections 4.2 and 4.4). Tabulated list of adverse reactions Adverse drug reactions (Table 1) are listed by MedDRA system organ class. Within each system organ class, the adverse drug reactions are ranked by frequency, with the most frequent reactions first. Within each frequency grouping, adverse drug reactions are presented in order of decreasing seriousness. In addition, the corresponding frequency category for each adverse drug reaction is based on the following convention (CIOMS III): 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). Table 1 Adverse drug reactions System organ class Frequency Preferred term* category Endocrine disorders Very common Adrenal insufficiency Metabolism and nutrition disorders Very common Hypokalaemia, decreased appetite Nervous system disorders Very common Dizziness, headache Common Syncope Cardiac disorders Common Tachycardia Vascular disorders Very common Hypotension Gastrointestinal disorders Very common Vomiting, nausea, diarrhoea, abdominal pain Skin and subcutaneous tissue disorders Very common Rash Common Hirsutism**, acne** Musculoskeletal and connective tissue Very common Myalgia disorders Arthralgia General disorders and administration Very common Fatigue, oedema site conditions Common Malaise Investigations Very common Blood testosterone increased**, blood corticotrophin increased Common Electrocardiogram QT prolonged, transaminases increased * Some terms denote grouped term of two or more MedDRA preferred terms that were considered clinically similar. The term “adrenal insufficiency” includes the terms glucocorticoid deficiency, adrenocortical insufficiency acute, steroid withdrawal syndrome, urine free cortisol decreased, cortisol decreased. ** Frequency “very common” in female patients. Description of selected adverse reactions CYP11B1 inhibition by osilodrostat is associated with adrenal steroid precursor accumulation and testosterone increases. In a clinical study with osilodrostat, mean testosterone levels in female patients increased from high normal at baseline to above the upper limit of the normal range. The increases reversed when treatment was interrupted. The testosterone increase was associated with mild to moderate cases of hirsutism or acne in a subset of patients. ACTH values above 10-fold upper limit of normal were observed in some Cushing’s disease patients treated with osilodrostat in the clinical studies (see section 5.1) and may be associated with cortisol values below the lower limit of normal. 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
שימוש לפי פנקס קופ''ח כללית 1994
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תאריך הכללה מקורי בסל
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