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

ANOREXIA ( 8 FDA reports)
FATIGUE ( 7 FDA reports)
HICCUPS ( 7 FDA reports)
PLATELET COUNT DECREASED ( 6 FDA reports)
DECREASED APPETITE ( 5 FDA reports)
ABNORMAL BEHAVIOUR ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
DELUSION ( 4 FDA reports)
HYPERTENSION ( 3 FDA reports)
MALAISE ( 3 FDA reports)
ACUTE PHOSPHATE NEPHROPATHY ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
SHOCK ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABULIA ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
FALL ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
METASTASES TO KIDNEY ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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