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

ARTHRALGIA ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
DIFFICULTY IN WALKING ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FALL ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CYSTITIS INTERSTITIAL ( 2 FDA reports)
COMMINUTED FRACTURE ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CHEST PAIN ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
INJURY ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
MYOPATHY TOXIC ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
GOUT ( 1 FDA reports)

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