Please choose an event type to view the corresponding MedsFacts report:

DYSPNOEA ( 17 FDA reports)
PNEUMONIA ( 14 FDA reports)
HEADACHE ( 13 FDA reports)
DIZZINESS ( 9 FDA reports)
DRUG INEFFECTIVE ( 9 FDA reports)
PAIN ( 9 FDA reports)
PYREXIA ( 8 FDA reports)
WEIGHT DECREASED ( 8 FDA reports)
EYE PAIN ( 7 FDA reports)
FATIGUE ( 7 FDA reports)
NAUSEA ( 7 FDA reports)
ARTHRALGIA ( 6 FDA reports)
COUGH ( 6 FDA reports)
DEPRESSED MOOD ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
URINARY TRACT INFECTION ( 6 FDA reports)
ASTHMA ( 5 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
GLAUCOMA ( 5 FDA reports)
HYPERHIDROSIS ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
ANAEMIA ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
BREAST CANCER ( 4 FDA reports)
BURNING SENSATION ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
DUODENAL ULCER ( 4 FDA reports)
EAR INFECTION ( 4 FDA reports)
EMPHYSEMA ( 4 FDA reports)
EYE DISORDER ( 4 FDA reports)
HIATUS HERNIA ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
LUNG INFECTION ( 4 FDA reports)
MEMORY IMPAIRMENT ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
ASTHENIA ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
DEATH ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
DYSSTASIA ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LUNG NEOPLASM ( 3 FDA reports)
MAJOR DEPRESSION ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MOTOR DYSFUNCTION ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ( 2 FDA reports)
BRADYPHRENIA ( 2 FDA reports)
BREAST CANCER FEMALE ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 2 FDA reports)
FRONTAL SINUS OPERATION ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
MELAENA ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SECRETION DISCHARGE ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
THIRST ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACNE ( 1 FDA reports)
ALLERGIC COUGH ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE LOSS ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
FALL ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OXYGEN SUPPLEMENTATION ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
ULCER ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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