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

HEPATIC FUNCTION ABNORMAL ( 7 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
ANOREXIA ( 5 FDA reports)
LIVER DISORDER ( 5 FDA reports)
RASH ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
VIRAL INFECTION ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PHARYNGITIS ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
AMNESIA ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
ENTERITIS INFECTIOUS ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
IRON DEFICIENCY ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
VITAMIN B12 DEFICIENCY ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ZINC DEFICIENCY ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYTHRODERMIC PSORIASIS ( 1 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROENTERITIS PSEUDOMONAS ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LARGE INTESTINE CARCINOMA ( 1 FDA reports)
LEUCINE AMINOPEPTIDASE INCREASED ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATIC CARCINOMA STAGE IV ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)

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