MedsFacts Reports covering ADVAIR (FLUTICASONE PROPIONATE, SALMETEROL XINAFOATE) INHALER
Directory listing ordered by most common adverse events for ADVAIR (FLUTICASONE PROPIONATE, SALMETEROL XINAFOATE) INHALER
Please choose an event type to view the corresponding MedsFacts report:
HEADACHE ( 5 FDA reports)
MALAISE ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
DIZZINESS ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DELUSION ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA LEGIONELLA ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN DISCOMFORT ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MALAISE ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
DIZZINESS ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DELUSION ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA LEGIONELLA ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN DISCOMFORT ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)