Serious adverse reactions that occurred in placebo-controlled studies in more than 1 subject and in greater percentage of subjects treated with placebo (n included (3 subjects vs. 0 The subjects experienced studies Malignancy were discontinued from the clinical 3 who (5.1)] (. 0.6% and also occurred more commonly in patients and Precautions 0.3%, respectively) / see treated with CINQAIR than placebo and Precautions 5.3) 1 Adverse reactions that occurred at greater than or equal to 2% incidence and more commonly than in the placebo group included. 1 event: oropharyngeal pain (2.6% vs. 2.2%).