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doi: 10.1016/j.tem.2018.09.001 33 KadouhHChedidVHalawiHBurtonDDClarkMMKhemaniDet al

Dulaglutides safety profile is consistent with other GLP-1 receptor agonists, with transient nausea being the most frequently reported adverse event (14.6% incidence). Dose escalation from 0.75 to 1.5 mg is recommended after at least four weeks, based on individual glycemic control needs [57]

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Using a larger needle to draw bacteriostatic water and solution from vials, then switching to your smaller injection needle preserves needle sharpness for more comfortable injections

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