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CEREBRAL INFARCTION ( 31 FDA reports)
CALCIPHYLAXIS ( 30 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 30 FDA reports)
PLATELET COUNT DECREASED ( 26 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 25 FDA reports)
ANAEMIA ( 21 FDA reports)
CARDIAC FAILURE ( 21 FDA reports)
BLOOD PRESSURE DECREASED ( 18 FDA reports)
URINARY TRACT INFECTION ( 18 FDA reports)
PYREXIA ( 16 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 14 FDA reports)
DYSPNOEA ( 14 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 13 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 12 FDA reports)
INFECTED SKIN ULCER ( 12 FDA reports)
PNEUMONIA ( 11 FDA reports)
VOMITING ( 11 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
BLOOD BILIRUBIN INCREASED ( 10 FDA reports)
RASH ( 10 FDA reports)
ABDOMINAL PAIN UPPER ( 9 FDA reports)
BLOOD CREATININE INCREASED ( 9 FDA reports)
BLOOD POTASSIUM INCREASED ( 9 FDA reports)
DIARRHOEA ( 9 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 9 FDA reports)
ERYTHEMA ( 9 FDA reports)
HYPOALBUMINAEMIA ( 9 FDA reports)
MULTI-ORGAN FAILURE ( 9 FDA reports)
HAEMATOCHEZIA ( 8 FDA reports)
LOSS OF CONSCIOUSNESS ( 8 FDA reports)
PERITONITIS ( 8 FDA reports)
RENAL IMPAIRMENT ( 8 FDA reports)
SMALL INTESTINAL PERFORATION ( 8 FDA reports)
TONIC CONVULSION ( 8 FDA reports)
VASCULAR PSEUDOANEURYSM ( 8 FDA reports)
ARTERIAL STENT INSERTION ( 7 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 7 FDA reports)
ENTEROSTOMY ( 7 FDA reports)
HAEMOGLOBIN DECREASED ( 7 FDA reports)
OESOPHAGOSTOMY ( 7 FDA reports)
RENAL FAILURE ( 7 FDA reports)
RENAL FAILURE ACUTE ( 7 FDA reports)
STENT REMOVAL ( 7 FDA reports)
SURGERY ( 7 FDA reports)
SURGICAL PROCEDURE REPEATED ( 7 FDA reports)
THROMBOCYTOPENIA ( 7 FDA reports)
ASCITES ( 6 FDA reports)
CEREBROVASCULAR DISORDER ( 6 FDA reports)
DECREASED APPETITE ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
FEBRILE NEUTROPENIA ( 6 FDA reports)
GLAUCOMA ( 6 FDA reports)
HAEMATURIA ( 6 FDA reports)
HEPATOSPLENOMEGALY ( 6 FDA reports)
HYPERURICAEMIA ( 6 FDA reports)
HYPOKALAEMIA ( 6 FDA reports)
NEUROLOGICAL SYMPTOM ( 6 FDA reports)
NEUTROPHIL COUNT INCREASED ( 6 FDA reports)
OESOPHAGEAL PERFORATION ( 6 FDA reports)
PLEURISY ( 6 FDA reports)
SKIN EXFOLIATION ( 6 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 6 FDA reports)
ANOREXIA ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
CORONARY ARTERY RESTENOSIS ( 5 FDA reports)
DELIRIUM ( 5 FDA reports)
DYSARTHRIA ( 5 FDA reports)
HAEMODYNAMIC INSTABILITY ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
HEMIPARESIS ( 5 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 5 FDA reports)
INTESTINAL ULCER ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
LIVER ABSCESS ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
NECROSIS ( 5 FDA reports)
PROTEIN TOTAL DECREASED ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
VISUAL FIELD DEFECT ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 4 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 4 FDA reports)
BONE MARROW FAILURE ( 4 FDA reports)
COUGH ( 4 FDA reports)
CROHN'S DISEASE ( 4 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
GENERALISED ERYTHEMA ( 4 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 4 FDA reports)
HEPATIC ENCEPHALOPATHY ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
HEPATITIS ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
ILEUS ( 4 FDA reports)
INFECTION ( 4 FDA reports)
LABORATORY TEST ABNORMAL ( 4 FDA reports)
LIP EROSION ( 4 FDA reports)
MALAISE ( 4 FDA reports)
MELAENA ( 4 FDA reports)
NIKOLSKY'S SIGN ( 4 FDA reports)
OCULAR HYPERAEMIA ( 4 FDA reports)
OEDEMA DUE TO RENAL DISEASE ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PETECHIAE ( 4 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
SCAB ( 4 FDA reports)
SCROTAL ULCER ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
SKIN ATROPHY ( 4 FDA reports)
SKIN DISCOLOURATION ( 4 FDA reports)
SKIN EROSION ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
TUMOUR LYSIS SYNDROME ( 4 FDA reports)
VENTRICULAR TACHYCARDIA ( 4 FDA reports)
WOUND ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD UREA ABNORMAL ( 3 FDA reports)
CARDIAC FAILURE ACUTE ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CARDIOVASCULAR DISORDER ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
DEATH ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
GASTROINTESTINAL OEDEMA ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
HEPATIC VEIN OCCLUSION ( 3 FDA reports)
HEPATOCELLULAR DAMAGE ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MOUTH HAEMORRHAGE ( 3 FDA reports)
MUSCLE ATROPHY ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
PERIPHERAL EMBOLISM ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 3 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
SUTURE RUPTURE ( 3 FDA reports)
THERAPEUTIC EMBOLISATION ( 3 FDA reports)
TORSADE DE POINTES ( 3 FDA reports)
TUMOUR HAEMORRHAGE ( 3 FDA reports)
TUMOUR NECROSIS ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED HEART ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
ENCEPHALITIS VIRAL ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FOETAL GROWTH RESTRICTION ( 2 FDA reports)
FUNGAEMIA ( 2 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL EXFOLIATION ( 2 FDA reports)
HAEMOBILIA ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERITONEAL HAEMORRHAGE ( 2 FDA reports)
PHLEBITIS INFECTIVE ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RETINOPATHY OF PREMATURITY ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SMALL FOR DATES BABY ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
AIRWAY PEAK PRESSURE INCREASED ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANAPHYLACTOID SHOCK ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CAPILLARY PERMEABILITY INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MUSCLE ABSCESS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERICARDITIS INFECTIVE ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SHOCK ( 1 FDA reports)
STRESS ( 1 FDA reports)
SWELLING ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VARICELLA ZOSTER VIRUS SEROLOGY POSITIVE ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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