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1C and D]) completed the 52-week open-label extension, with the most common reasons for the study discontinuation attributed to adverse events (study 301: 23.4%
doi: 10.25270/jic/24.00351 Villegas Katrina
Son dng kch mu mi PCD l mt trong nhng "con cng" ca thng hiu PCD
Fortalecimiento general del organismo
C.DejemliA.DelvinE.ZhangJ
The FDA-approved dose of 1.75 mg was chosen partly to balance efficacy against the nausea rate seen at higher doses in early trials
