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

DIARRHOEA ( 23 FDA reports)
COLITIS ULCERATIVE ( 11 FDA reports)
DECREASED APPETITE ( 10 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 10 FDA reports)
PLATELET COUNT DECREASED ( 10 FDA reports)
PNEUMONIA ( 10 FDA reports)
PYREXIA ( 10 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 9 FDA reports)
COUGH ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
LIVER DISORDER ( 7 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
SEPSIS ( 6 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 6 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
ILEUS PARALYTIC ( 5 FDA reports)
MALAISE ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
ENTERITIS INFECTIOUS ( 4 FDA reports)
HYPOCALCAEMIA ( 4 FDA reports)
NEOPLASM PROGRESSION ( 4 FDA reports)
NEUTROPHIL COUNT DECREASED ( 4 FDA reports)
PANCREATITIS ACUTE ( 4 FDA reports)
PARONYCHIA ( 4 FDA reports)
SHOCK ( 4 FDA reports)
VIRAL INFECTION ( 4 FDA reports)
ANOREXIA ( 3 FDA reports)
AORTIC DISSECTION ( 3 FDA reports)
ASCITES ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
EYELID OEDEMA ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
HYPOMAGNESAEMIA ( 3 FDA reports)
LARGE INTESTINE PERFORATION ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SUBILEUS ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BIOPSY ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 2 FDA reports)
COLITIS COLLAGENOUS ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
ILEUS ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
PAIN ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
RASH ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TETANY ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TREMOR ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BED REST ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTASES TO RETROPERITONEUM ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OCCULT BLOOD ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RECTAL CANCER METASTATIC ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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