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

DEPRESSED LEVEL OF CONSCIOUSNESS ( 10 FDA reports)
HAEMOGLOBIN DECREASED ( 10 FDA reports)
INTERSTITIAL LUNG DISEASE ( 10 FDA reports)
PLATELET COUNT DECREASED ( 10 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 10 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 9 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 8 FDA reports)
RHABDOMYOLYSIS ( 8 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
CARDIAC FAILURE ( 7 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 6 FDA reports)
HAEMODIALYSIS ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 5 FDA reports)
BLOOD POTASSIUM INCREASED ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
HAEMATOCRIT DECREASED ( 5 FDA reports)
HEPATITIS FULMINANT ( 5 FDA reports)
HYPERGLYCAEMIA ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
BLOOD SODIUM DECREASED ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 4 FDA reports)
MALAISE ( 4 FDA reports)
PNEUMONIA ASPIRATION ( 4 FDA reports)
SHOCK ( 4 FDA reports)
SINUS ARREST ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HYPOCOAGULABLE STATE ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 3 FDA reports)
MELAENA ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
POLYURIA ( 3 FDA reports)
RASH ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
STRIDOR ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
AFFECTIVE DISORDER ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CEREBRAL THROMBOSIS ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
COMMUNICATION DISORDER ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
EXTRADURAL HAEMATOMA ( 2 FDA reports)
FALL ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTRODUODENAL ULCER ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC INFARCTION ( 2 FDA reports)
HYPOALDOSTERONISM ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 2 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 2 FDA reports)
METABOLIC ALKALOSIS ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PARAPLEGIA ( 2 FDA reports)
PLATELET COUNT ABNORMAL ( 2 FDA reports)
POLYDIPSIA ( 2 FDA reports)
POSTURE ABNORMAL ( 2 FDA reports)
PSEUDO-BARTTER SYNDROME ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
STARING ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY INCREASED ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BASOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD THROMBIN DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BLUE TOE SYNDROME ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
COMA ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
COUGH ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYCLIC NEUTROPENIA ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAT EMBOLISM ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GINGIVAL HYPERTROPHY ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LAXATIVE ABUSE ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST NEGATIVE ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
POLYP ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RETINOPATHY HYPERTENSIVE ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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