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

CARDIAC FAILURE ( 43 FDA reports)
PNEUMONIA ( 20 FDA reports)
BLOOD CREATININE INCREASED ( 18 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 16 FDA reports)
BLOOD UREA INCREASED ( 15 FDA reports)
ANAEMIA ( 14 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 14 FDA reports)
PLATELET COUNT DECREASED ( 13 FDA reports)
DIZZINESS ( 11 FDA reports)
RIGHT VENTRICULAR FAILURE ( 11 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
FALL ( 9 FDA reports)
MALAISE ( 9 FDA reports)
MULTI-ORGAN FAILURE ( 9 FDA reports)
PYREXIA ( 9 FDA reports)
RENAL FAILURE ACUTE ( 9 FDA reports)
RENAL IMPAIRMENT ( 9 FDA reports)
BLOOD PRESSURE DECREASED ( 8 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 8 FDA reports)
BRADYCARDIA ( 7 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
INFECTION ( 7 FDA reports)
INTERSTITIAL LUNG DISEASE ( 7 FDA reports)
RHABDOMYOLYSIS ( 7 FDA reports)
BLOOD POTASSIUM INCREASED ( 6 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 6 FDA reports)
COUGH ( 6 FDA reports)
DYSPNOEA EXERTIONAL ( 6 FDA reports)
EJECTION FRACTION DECREASED ( 6 FDA reports)
HYPOXIA ( 6 FDA reports)
LIVER DISORDER ( 6 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 5 FDA reports)
CEREBRAL INFARCTION ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
DEATH ( 5 FDA reports)
DECREASED APPETITE ( 5 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
ENDOTRACHEAL INTUBATION ( 5 FDA reports)
GASTROENTERITIS ( 5 FDA reports)
HYPERHIDROSIS ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 5 FDA reports)
NERVOUS SYSTEM DISORDER ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
ORTHOPNOEA ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
SPEECH DISORDER ( 5 FDA reports)
VENTRICULAR TACHYCARDIA ( 5 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
CARDIOMEGALY ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HYPERTHYROIDISM ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
MYELODYSPLASTIC SYNDROME ( 4 FDA reports)
PNEUMOTHORAX ( 4 FDA reports)
POST PROCEDURAL HAEMATOMA ( 4 FDA reports)
PULMONARY HYPERTENSION ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
VOMITING ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
ACUTE RESPIRATORY FAILURE ( 3 FDA reports)
ANGIOPATHY ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ASPHYXIA ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
BACTERAEMIA ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD URIC ACID INCREASED ( 3 FDA reports)
CARDIOGENIC SHOCK ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
DYSLALIA ( 3 FDA reports)
EPIGASTRIC DISCOMFORT ( 3 FDA reports)
FUNGAL SEPSIS ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPERPROLACTINAEMIA ( 3 FDA reports)
HYPERTENSIVE HEART DISEASE ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPOCHROMIC ANAEMIA ( 3 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
MARASMUS ( 3 FDA reports)
MOBILITY DECREASED ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 3 FDA reports)
PITUITARY TUMOUR BENIGN ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SPUTUM ABNORMAL ( 3 FDA reports)
STOMACH DISCOMFORT ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
CARDIAC FAILURE CHRONIC ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
ERYTHROPENIA ( 2 FDA reports)
FOLATE DEFICIENCY ( 2 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 2 FDA reports)
JOINT ARTHROPLASTY ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LYMPHADENITIS ( 2 FDA reports)
NERVE BLOCK ( 2 FDA reports)
NOCTURNAL DYSPNOEA ( 2 FDA reports)
PHLEBITIS INFECTIVE ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
SINUS ARREST ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
YAWNING ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY ARTERY DILATATION ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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