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Vipdomet
Eintrag öffnenVipdomet · 4.1 Therapeutic indications · 1
Eintrag öffnenVipdomet · 4.3 Contraindications · 1
Eintrag öffnenVipdomet · 4.3 · - Hypersensitivity to the active substances or to any of the excipients listed in section 6.1 or history of a
Eintrag öffnenVipdomet · 4.4 Special warnings and precautions for use · 1
Eintrag öffnenVipdomet · 4.5 Interaction with other medicinal products and other forms of interaction · 1
Eintrag öffnenVipdomet · 4.5 · 7 Iodinated contrast agents Vipdomet must be discontinued prior to or at the time of the imaging procedure and
Eintrag öffnenVipdomet · 4.5 · 8 In clinical studies, alogliptin had no clinically relevant effect on the pharmacokinetics of caffeine, (R)-w
Eintrag öffnenVipdomet · 4.5 · ACE inhibitors ACE inhibitors may decrease blood glucose levels. If necessary, the dose of Vipdomet should be
Eintrag öffnenVipdomet · 4.5 · Alcohol Alcohol intoxication is associated with an increased risk of lactic acidosis, particularly in case of
Eintrag öffnenVipdomet · 4.5 · Alogliptin is primarily excreted unchanged in the urine and metabolism by the cytochrome (CYP) P450 enzyme sys
Eintrag öffnenVipdomet · 4.5 · Cationic medicinal products Cationic substances that are eliminated by renal tubular secretion (e.g. cimetidin
Eintrag öffnenVipdomet · 4.5 · Co-administration of 100 mg alogliptin once daily and 1 000 mg metformin hydrochloride twice daily for 6 days
Eintrag öffnenVipdomet · 4.5 · Combination of alogliptin with other anti-diabetic medicinal products
Eintrag öffnenVipdomet · 4.5 · Combination requiring precautions for use
Eintrag öffnenVipdomet · 4.5 · Concomitant use not recommended
Eintrag öffnenVipdomet · 4.5 · Effects of alogliptin on other medicinal products
Eintrag öffnenVipdomet · 4.5 · Effects of other medicinal products on alogliptin
Eintrag öffnenVipdomet · 4.5 · In healthy subjects, alogliptin had no effect on prothrombin time or International Normalised Ratio (INR) when
Eintrag öffnenVipdomet · 4.5 · In vitro studies suggest that alogliptin does not inhibit nor induce CYP 450 isoforms at concentrations achiev
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