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

HEPATIC FUNCTION ABNORMAL ( 11 FDA reports)
PYREXIA ( 11 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
DIARRHOEA ( 8 FDA reports)
SEPTIC SHOCK ( 8 FDA reports)
HYPERTENSION ( 7 FDA reports)
BLOOD BILIRUBIN INCREASED ( 6 FDA reports)
CARDIAC ARREST ( 6 FDA reports)
PETECHIAE ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 5 FDA reports)
BLOOD PRESSURE DECREASED ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
HYPOKALAEMIA ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
PURPURA ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
PARKINSONISM ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 3 FDA reports)
ANXIETY DISORDER ( 3 FDA reports)
ASCITES ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
CAPILLARY LEAK SYNDROME ( 3 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
CLOSTRIDIUM COLITIS ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
CYSTITIS HAEMORRHAGIC ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
ENGRAFT FAILURE ( 3 FDA reports)
FALL ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
GLAUCOMA ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
HEPATORENAL SYNDROME ( 3 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPOPROTEINAEMIA ( 3 FDA reports)
HYPOPROTHROMBINAEMIA ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
KLEBSIELLA INFECTION ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PROTEIN TOTAL DECREASED ( 3 FDA reports)
RASH ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 3 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTERIAL HAEMORRHAGE ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
DECREASED VENTRICULAR PRELOAD ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GASTRODUODENITIS ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HOARSENESS ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPHAEMA ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
LIP EROSION ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
PERICARDIAL HAEMORRHAGE ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
REFLUX OESOPHAGITIS ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
SCAB ( 2 FDA reports)
SCROTAL ULCER ( 2 FDA reports)
SKIN ATROPHY ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN EROSION ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
URATE NEPHROPATHY ( 2 FDA reports)
VARICES OESOPHAGEAL ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
WOUND ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ENDOTOXIC SHOCK ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAND DERMATITIS ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MICTURITION FREQUENCY DECREASED ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINARY NITROGEN INCREASED ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use