Quest for the right Drug
קטוקונזול HRA 200 מ"ג KETOCONAZOLE HRA 200 MG (KETOCONAZOLE)
תרופה במרשם
תרופה בסל
נרקוטיקה
ציטוטוקסיקה
צורת מתן:
פומי : PER OS
צורת מינון:
טבליה : 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
Contraindications : התוויות נגד
4.3 Contraindications - Hypersensitivity to the active substance or to any of the excipients listed in section 6.1 - Hypersensitivity to any imidazole antifungal medication product; - Acute or chronic liver disease and/or if pre-treatment liver enzymes levels are above 2 times the upper limit of normal (see sections 4.2 and 4.4) - Pregnancy (see section 4.6) - Breastfeeding (see section 4.6) - Congenital or documented acquired QTc prolongation - Concomitant therapy with any of the following medicinal products which may interact and result in potentially life-threatening adverse reactions (see section 4.5): o CYP3A4 metabolised HMG-CoA reductase inhibitors (e.g. simvastatin, atorvastatin and lovastatin) due to an increased risk of skeletal muscle toxicity including rhabdomyolysis o eplerenone due to an increased risk of hyperkalemia and hypotension o substances that may have their plasma concentrations increased and have QT prolonging potential : methadone, disopyramide, quinidine, dronedarone, pimozide, sertindole, saquinavir (saquinavir/ritonavir 1000/100 mg bid), ranolazine, mizolastine, halofantrine o dabigatran due to an increased bleeding risk o triazolam, oral midazolam and alprazolam due to potential for prolonged or increased sedation and respiratory depression o ergot alkaloids (e.g. dihydroergotamine, ergometrine (ergonovine), ergotamine and methylergometrine (methylergonovine) due to an increased risk of ergotism and other serious vasospastic adverse reactions o lurasidone o quetiapine due to an increased risk of toxicity o telithromycin and clarithromycin in patients with severe renal impairment due to an increased risk of hepatotoxicity and QT interval prolongation o felodipine, nisoldipine due to an increased risk of oedema and congestive heart failure o colchicine in patients with renal impairment due to an increased risk of severe adverse reactions o irinotecan due to an alteration of the metabolism of this medicinal product o everolimus, sirolimus (also known as rapamycin) due to an increase of the plasma concentrations of these medicinal products o vardenafil in men older than 75-years due to increased risk of adverse reactions o paritaprevir/ombitasvir (ritonavir) due to increased risk of adverse reactions o fesoterodine and solifenacin in patients with renal impairment o tolvaptan used for a specific disease called “syndrome of inappropriate antidiuretic hormone secretion”. The list above is not an inclusive list of compounds that may interact with ketoconazole and result in potentially life-threatening reactions.
שימוש לפי פנקס קופ''ח כללית 1994
לא צוין
תאריך הכללה מקורי בסל
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הגבלות
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מידע נוסף