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

RENAL FAILURE ( 10 FDA reports)
DIARRHOEA ( 9 FDA reports)
NAUSEA ( 8 FDA reports)
VOMITING ( 6 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
RHABDOMYOLYSIS ( 5 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
OSTEONECROSIS ( 4 FDA reports)
TRANSAMINASES INCREASED ( 4 FDA reports)
TREMOR ( 4 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 3 FDA reports)
HEPATORENAL SYNDROME ( 3 FDA reports)
ICTERUS INDEX INCREASED ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
PALLOR ( 3 FDA reports)
RASH ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
AGITATION ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CHILLS ( 2 FDA reports)
COUGH ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ENTERITIS ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HYDROTHORAX ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
ULCER HAEMORRHAGE ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
DEATH ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
GASTRIC OPERATION ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
MESOTHELIOMA MALIGNANT ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
SCLEROTHERAPY ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)

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