MedsFacts Reports covering ADVAIR DISKUS (SERETIDE MITE)
Directory listing ordered by most common adverse events for ADVAIR DISKUS (SERETIDE MITE)
Please choose an event type to view the corresponding MedsFacts report:
PNEUMONIA ( 8 FDA reports)
PULMONARY EMBOLISM ( 7 FDA reports)
DYSPNOEA ( 6 FDA reports)
FALL ( 6 FDA reports)
ASTHENIA ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
ANAEMIA ( 4 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 4 FDA reports)
COUGH ( 4 FDA reports)
EJECTION FRACTION DECREASED ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
BACK PAIN ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PAIN ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
TROPONIN INCREASED ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BUNDLE BRANCH BLOCK ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
FACIAL BONES FRACTURE ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VENOUS OCCLUSION ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACNE ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CYST ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPENDENCE ON RESPIRATOR ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DIVERTICULAR FISTULA ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROINTESTINAL FISTULA ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PELVIC HAEMATOMA ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHARYNGEAL INJURY ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYELOCALIECTASIS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VENOUS STASIS ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WOUND ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
PULMONARY EMBOLISM ( 7 FDA reports)
DYSPNOEA ( 6 FDA reports)
FALL ( 6 FDA reports)
ASTHENIA ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
ANAEMIA ( 4 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 4 FDA reports)
COUGH ( 4 FDA reports)
EJECTION FRACTION DECREASED ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
BACK PAIN ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PAIN ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
TROPONIN INCREASED ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BUNDLE BRANCH BLOCK ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
FACIAL BONES FRACTURE ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VENOUS OCCLUSION ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACNE ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CYST ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPENDENCE ON RESPIRATOR ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DIVERTICULAR FISTULA ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBROUS DYSPLASIA OF BONE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROINTESTINAL FISTULA ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PELVIC HAEMATOMA ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHARYNGEAL INJURY ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYELOCALIECTASIS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VENOUS STASIS ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WOUND ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)