Adverse events reported by less than 3% of the patients receiving PROVENTIL HFA Inhalation Aerosol, and by a greater proportion of PROVENTIL HFA Inhalation Aerosol patients than placebo patients, which have the potential to be related to PROVENTIL HFA Inhalation Aerosol include: dysphonia , increased sweating, dry mouth , chest pain, edema, rigors, ataxia , leg cramps, hyperkinesia, eructation , flatulence , tinnitus , diabetes mellitus , anxiety, depression, somnolence , rash. Palpitation and dizziness have also been observed with PROVENTIL HFA Inhalation Aerosol.
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Other adverse reactions occurring in the group receiving SEREVENT DISKUS that occurred at a frequency of ≥ 1% and were more common than in the placebo group were as follows: anxiety; arthralgia and articular rheumatism; bone and skeletal pain; candidiasis mouth/throat; dental discomfort and pain; dyspeptic symptoms; edema and swelling; gastrointestinal infections; hyperglycemia ; hyposalivation; keratitis and conjunctivitis ; lower respiratory signs and symptoms; migraines; muscle pain; muscle stiffness, tightness, and rigidity; musculoskeletal inflammation; pain; and skin rashes.