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. 2018 Nov 30;10(1):5–19. doi: 10.1007/s13300-018-0535-9

Table 2.

Dosage and administration requirements for glucagon-like peptide-1 receptor agonists based on European Union summary of product characteristics of each agent

Drug Titration Initial dosage Recommended dosage Administration in relation to meals Missed dose
Once-daily
 Exenatide Yes 5 mcg BID for at least 1 month 5–10 mcg BIDb Should be administered within 60 min before main meals Continue with the next scheduled dose
 Liraglutide Yes 0.6 mg OD for at least 1 week 1.2–1.8 mg ODc At any time, without regard to meals

≤ 12 h: administer the dose as soon as possible

> 12 h: skip the dose

 Lixisenatide Yes 10 mcg OD for 14 days 20 mcg OD Should be administered within 60 min before any meal Administer the dose within 1 h before the next meal
Once-weekly
 Exenatide No Not applicable 2 mg once weekly At any time, without regard to meals Administer the next dose as soon as practical. Only one injection should be administered in a 24-h period
 Dulaglutide Noa Not applicable

Monotherapy: 0.75 mg once weekly

Add-on therapy: 1.5 mg once weekly

At any time, without regard to meals

≥ 3 days until the next scheduled dose: administer the dose as soon as possible

< 3 days: skip the dose, wait and administer their next regularly scheduled weekly dose

 Semaglutide Yes 0.25 mg once weekly for 4 weeks 0.5–1.0 mg once weekly (dose increase after 4 weeks if required) At any time, without regard to meals

≥ 5 days until the next scheduled dose: administer the dose as soon as possible

< 5 days: skip the dose, wait and administer their next regularly scheduled weekly dose

Data were extracted from references [1520, 30]

BID Twice a day, OD once daily

aIn elderly patients, a lower dose of 0.75 mg once weekly can be considered

bImmediate-release exenatide should be initiated at 5 mcg per dose administered BID for at least 1 month to improve tolerability; the dose can then be increased to 10 mcg BID to further improve glycemic control

cLiraglutide should be initiated at a dose of 0.6 mg daily to improve gastrointestinal tolerability; after at least 1 week, the dose should be increased to 1.2 mg and a further increase to 1.8 mg may be required to further improve glycemic control