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

MYELOFIBROSIS ( 25 FDA reports)
DRUG INTERACTION ( 13 FDA reports)
RENAL FAILURE ( 13 FDA reports)
PLATELET COUNT INCREASED ( 12 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 11 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 10 FDA reports)
TACHYCARDIA ( 9 FDA reports)
ANAEMIA ( 8 FDA reports)
CARDIAC FAILURE ( 8 FDA reports)
ACUTE CORONARY SYNDROME ( 7 FDA reports)
ATRIAL FIBRILLATION ( 7 FDA reports)
ARRHYTHMIA ( 6 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
HAEMATEMESIS ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
MYELODYSPLASTIC SYNDROME ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 5 FDA reports)
MALLORY-WEISS SYNDROME ( 5 FDA reports)
PANCYTOPENIA ( 5 FDA reports)
SKIN ULCER ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BLADDER CANCER ( 4 FDA reports)
CEREBRAL HAEMORRHAGE ( 4 FDA reports)
HAEMATURIA ( 4 FDA reports)
MALAISE ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 4 FDA reports)
VERTIGO ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
FALL ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HIATUS HERNIA ( 3 FDA reports)
MELAENA ( 3 FDA reports)
MUCOUS STOOLS ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PULMONARY HYPERTENSION ( 3 FDA reports)
SUBDURAL HAEMORRHAGE ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
ARTERITIS CORONARY ( 2 FDA reports)
ATRIAL THROMBOSIS ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CHORDAE TENDINAE RUPTURE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
GASTRIC ULCER HELICOBACTER ( 2 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
GASTROINTESTINAL ULCER ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
NEOPLASM PROSTATE ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SCAB ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
TORSADE DE POINTES ( 2 FDA reports)
VITILIGO ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CAUDA EQUINA SYNDROME ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
COMA ( 1 FDA reports)
CONGENITAL ABSENCE OF VERTEBRA ( 1 FDA reports)
COUGH ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CRYOGLOBULINAEMIA ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
INJURY ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MEGAKARYOCYTES ABNORMAL ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHROANGIOSCLEROSIS ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROSTATE CANCER RECURRENT ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETROPERITONEAL FIBROSIS ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SPONTANEOUS HAEMATOMA ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
TONGUE NEOPLASM ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
TRICUSPID VALVE DISEASE ( 1 FDA reports)
ULCER ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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