Gegenanzeigen · Janumet
Janumet 50 mg/850 mg film-coated tablets Janumet 50 mg/1 000 mg film-coated tablets · Abschnitt 4.3 · PDF-Seite 4
HOS-119358 · Präparat HOS-094931
- hypersensitivity to the active substances or to any of the excipients listed in section 6.1 (see sections 4.4 and 4.8); - any type of acute metabolic acidosis (such as lactic acidosis, diabetic ketoacidosis); - diabetic pre-coma; - severe renal failure (GFR< 30 mL/min) (see section 4.4); - acute conditions with the potential to alter renal function such as: - dehydration, - severe infection, - shock, - intravascular administration of iodinated contrast agents (see section 4.4); - acute or chronic disease which may cause tissue hypoxia such as: - cardiac or respiratory failure, - recent myocardial infarction, - shock; - hepatic impairment; - acute alcohol intoxication, alcoholism; - breast-feeding.
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Vollständigen Kontext in der EMA-Fachinformation lesen →Quellennachweis
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