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To view a copy of this licence, visit About this article Cite this article Abd Elkader, HT.A.E., Hussein, M.M., Mohammed, N.A
An open-label study of the long-term safety of pirfenidone in patients with idiopathic pulmonary fibrosis (RECAP)
Patients should be informed that gastrointestinal symptoms are dose dependent, common during treatment initiation and escalation, usually transient, influenced by the starting dose, and speed of titration ( Adjunctive dietary and behavioral measures may aid during treatment initiation and dose escalation
Eli Lilly is the parent company of exenatide, the first GLP-1 RA
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However, in the exenatide treatment group, the primary outcome rate was 61.2% (n=170), compared to 56.7% in the standard treatment group (n=171), with an adjusted ratio of 1.22 [95% CI, 0.79-1.88] (P=0.38)., which meant that the proportion of subjects who achieved the desired effect in exenatide treatment group was higher (110)
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