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

WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
CLOSTRIDIUM COLITIS ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PROTEIN TOTAL DECREASED ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
ASTHENIA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PITTING OEDEMA ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE SARCOMA ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
FISTULA ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFUSION SITE INFLAMMATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
LACTOBACILLUS TEST POSITIVE ( 1 FDA reports)
MELAENA ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OSTEOPOROTIC FRACTURE ( 1 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
RADIATION SKIN INJURY ( 1 FDA reports)
RASH ( 1 FDA reports)
RECURRENT CANCER ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SPINDLE CELL SARCOMA ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
UTERINE CANCER ( 1 FDA reports)
VANISHING BILE DUCT SYNDROME ( 1 FDA reports)

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