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

RHABDOMYOLYSIS ( 29 FDA reports)
DRUG INTERACTION ( 27 FDA reports)
CYTOLYTIC HEPATITIS ( 18 FDA reports)
PRURITUS ( 14 FDA reports)
MYALGIA ( 13 FDA reports)
RENAL FAILURE ( 13 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 12 FDA reports)
HYPERKALAEMIA ( 12 FDA reports)
PYREXIA ( 12 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
DIARRHOEA ( 11 FDA reports)
EOSINOPHILIA ( 11 FDA reports)
PULMONARY EMBOLISM ( 11 FDA reports)
ASTHENIA ( 10 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 10 FDA reports)
OEDEMA PERIPHERAL ( 10 FDA reports)
RECTAL HAEMORRHAGE ( 10 FDA reports)
RENAL FAILURE ACUTE ( 10 FDA reports)
AGITATION ( 9 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
PANCREATIC CARCINOMA ( 9 FDA reports)
ANAEMIA ( 8 FDA reports)
DEEP VEIN THROMBOSIS ( 8 FDA reports)
HEADACHE ( 8 FDA reports)
RASH ERYTHEMATOUS ( 8 FDA reports)
CHOLELITHIASIS ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
HYPONATRAEMIA ( 7 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 7 FDA reports)
PANCREATITIS ACUTE ( 7 FDA reports)
PEMPHIGOID ( 7 FDA reports)
RASH MACULO-PAPULAR ( 7 FDA reports)
THROMBOCYTOPENIA ( 7 FDA reports)
ARTHRALGIA ( 6 FDA reports)
CARDIAC FAILURE ( 6 FDA reports)
CHOLESTASIS ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 6 FDA reports)
INTERSTITIAL LUNG DISEASE ( 6 FDA reports)
MYELODYSPLASTIC SYNDROME ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
PURPURA ( 6 FDA reports)
VENTRICULAR ARRHYTHMIA ( 6 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HYPERHIDROSIS ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
MALAISE ( 5 FDA reports)
NEPHROTIC SYNDROME ( 5 FDA reports)
THROMBOSIS IN DEVICE ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 4 FDA reports)
ACUTE PULMONARY OEDEMA ( 4 FDA reports)
ANAEMIA MACROCYTIC ( 4 FDA reports)
ANGIOEDEMA ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK ( 4 FDA reports)
BILIARY DILATATION ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
COGNITIVE DISORDER ( 4 FDA reports)
COLITIS ( 4 FDA reports)
COLON CANCER RECURRENT ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DIABETIC KETOACIDOSIS ( 4 FDA reports)
DIABETIC NEPHROPATHY ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
ECZEMA ( 4 FDA reports)
ERYTHEMA NODOSUM ( 4 FDA reports)
FALL ( 4 FDA reports)
HAEMATOMA ( 4 FDA reports)
HEPATITIS ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
INTESTINAL INFARCTION ( 4 FDA reports)
LYMPHOMA ( 4 FDA reports)
MAJOR DEPRESSION ( 4 FDA reports)
MUSCLE RUPTURE ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
PERITONITIS ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
SHOCK ( 4 FDA reports)
TOXIC SKIN ERUPTION ( 4 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 4 FDA reports)
VERTIGO ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
APHASIA ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BLADDER CANCER ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CAESAREAN SECTION ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CARDIOGENIC SHOCK ( 3 FDA reports)
CARPAL TUNNEL SYNDROME ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CHILLS ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DISSOCIATION ( 3 FDA reports)
DUODENAL ULCER ( 3 FDA reports)
ERYTHEMA MULTIFORME ( 3 FDA reports)
FOETAL DISORDER ( 3 FDA reports)
FOETAL HEART RATE DECELERATION ( 3 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HEPATITIS CHOLESTATIC ( 3 FDA reports)
HYPERNATRAEMIA ( 3 FDA reports)
ILEAL PERFORATION ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
MELAENA ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
MYOGLOBIN BLOOD PRESENT ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PNEUMOPERITONEUM ( 3 FDA reports)
RASH MORBILLIFORM ( 3 FDA reports)
RENAL COLIC ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
RETINAL DETACHMENT ( 3 FDA reports)
TALIPES ( 3 FDA reports)
TENDONITIS ( 3 FDA reports)
THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ADHESION ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANURIA ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
COMA ( 2 FDA reports)
CRANIAL SUTURES WIDENING ( 2 FDA reports)
DEATH ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FIBRIN D DIMER INCREASED ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
LICHENOID KERATOSIS ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
MASTOIDITIS ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 2 FDA reports)
OLIGOHYDRAMNIOS ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
RASH ( 2 FDA reports)
RECTOSIGMOID CANCER ( 2 FDA reports)
SENSE OF OPPRESSION ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SINOATRIAL BLOCK ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TENDON RUPTURE ( 2 FDA reports)
VASCULAR PURPURA ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BRONCHIAL WALL THICKENING ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CRYOGLOBULINAEMIA ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DIVERTICULUM DUODENAL ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
EPIDURITIS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JEJUNAL ULCER ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KIDNEY MALFORMATION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MENINGORRHAGIA ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MONARTHRITIS ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOGLOBINAEMIA ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PARONYCHIA ( 1 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
PEPTIC ULCER PERFORATION ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PSEUDOLYMPHOMA ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKULL MALFORMATION ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRANSFERRIN INCREASED ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URTICARIA PAPULAR ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VIRAL PERICARDITIS ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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