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

CARDIAC FAILURE ( 18 FDA reports)
RENAL FAILURE ACUTE ( 15 FDA reports)
CONDITION AGGRAVATED ( 11 FDA reports)
DIARRHOEA ( 11 FDA reports)
DRUG INTERACTION ( 10 FDA reports)
RENAL FAILURE ( 9 FDA reports)
ARTHRALGIA ( 7 FDA reports)
FATIGUE ( 7 FDA reports)
HYPERTENSIVE CRISIS ( 6 FDA reports)
DIZZINESS ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
EOSINOPHILIA ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
HYPERKALAEMIA ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
RASH ( 5 FDA reports)
RENAL IMPAIRMENT ( 5 FDA reports)
ANAEMIA ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
CHOLESTASIS ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DERMATITIS BULLOUS ( 4 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
FALL ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HYPOSIDERAEMIA ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
LIVER INJURY ( 4 FDA reports)
LYMPHOPENIA ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
STEVENS-JOHNSON SYNDROME ( 4 FDA reports)
TOXIC SKIN ERUPTION ( 4 FDA reports)
ACIDOSIS ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BLINDNESS UNILATERAL ( 3 FDA reports)
BLISTER ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
CYTOLYTIC HEPATITIS ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DERMATITIS ALLERGIC ( 3 FDA reports)
EXTRASYSTOLES ( 3 FDA reports)
GOUT ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
ISCHAEMIC STROKE ( 3 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
ODYNOPHAGIA ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
PHOTOSENSITIVITY REACTION ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ACUTE PRERENAL FAILURE ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
COMA ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GOUTY ARTHRITIS ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HYPOCHROMIC ANAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
MICROCYTIC ANAEMIA ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PROSTATE CANCER RECURRENT ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
TESTICULAR PAIN ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VASCULITIS NECROTISING ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APOPTOSIS ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BILIARY POLYP ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOSCOPY ABNORMAL ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHONDROCALCINOSIS ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC VEIN DILATATION ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LIBIDO DISORDER ( 1 FDA reports)
LICHEN SCLEROSUS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MECHANICAL VENTILATION COMPLICATION ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
MICROSCOPIC POLYANGIITIS ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSTEITIS DEFORMANS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
PROSTATITIS ESCHERICHIA COLI ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RASH SCARLATINIFORM ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
REFRACTORINESS TO PLATELET TRANSFUSION ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
SEBORRHOEIC DERMATITIS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TREMOR ( 1 FDA reports)
ULCER ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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