Voorbeelden van het gebruik van Onglyza in het Engels en hun vertalingen in het Nederlands
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Saxagliptin has been authorised in the EU as Onglyza since 2009.
It is not known if Onglyza passes into human breast milk.
The other ingredients are What Onglyza looks like and contents of the pack.
Onglyza 2.5 mg film-coated tablets are pale yellow to light yellow, biconvex, round.
If you are having haemodialysis then Onglyza is not recommended for you. if you have moderate
The safety and efficacy of Onglyza in children aged birth to< 18 years have not yet been established.
the event rates for Onglyza and placebo did not diverge notably over time.
Table 2 Key efficacy results of Onglyza 5 mg per day in placebo-controlled monotherapy trials
The SAVOR trial included 8240 patients treated with Onglyza 5 mg or 2.5 mg once daily and 8173 patients on placebo.
The overall incidence of adverse events in patients treated with Onglyza in this trial was similar to placebo 72.5% versus 72.2%, respectively.
Onglyza must not be used in patients who have had any serious hypersensitivity reaction to a dipeptidyl peptidase-4(DPP4) inhibitor see section 4.3.
The company also provided studies that were used in the authorisation of Forxiga and Onglyza where saxagliptin
was 17.1% in subjects treated with Onglyza and 14.8% among patients treated with placebo.
add-on combination therapy with metformin plus sulphonylurea, the overall incidence of reported hypoglycemia was 10.1% for Onglyza 5 mg and 6.3% for placebo.
the overall incidence of reported hypoglycaemia was 18.4% for Onglyza 5 mg and 19.9% for placebo.
Onglyza 5 mg tablets are pink,
When Onglyza is used in combination with insulin
Onglyza 2.5 mg tablets are pale yellow to light yellow,
Caution is warranted if Onglyza is used in patients who have known risk factors for hospitalization for heart failure,
including 3,021 patients treated with Onglyza, randomised in six double-blind,