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

BLOOD UREA INCREASED ( 8 FDA reports)
CARDIAC FAILURE ( 8 FDA reports)
MALAISE ( 8 FDA reports)
BLOOD CREATININE INCREASED ( 7 FDA reports)
FALL ( 7 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 7 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
GAIT DISTURBANCE ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
RHABDOMYOLYSIS ( 6 FDA reports)
BACK DISORDER ( 5 FDA reports)
DELUSION ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
DYSKINESIA ( 5 FDA reports)
FIBRIN D DIMER INCREASED ( 5 FDA reports)
GASTRIC ULCER ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
IRON DEFICIENCY ANAEMIA ( 5 FDA reports)
MOUTH ULCERATION ( 5 FDA reports)
MOVEMENT DISORDER ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 5 FDA reports)
NEUROGENIC BLADDER ( 5 FDA reports)
TONGUE ULCERATION ( 5 FDA reports)
ASCITES ( 4 FDA reports)
BLOOD IRON DECREASED ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
ILEUS ( 4 FDA reports)
OSTEOARTHRITIS ( 4 FDA reports)
RASH ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 4 FDA reports)
SERUM FERRITIN DECREASED ( 4 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD URIC ACID INCREASED ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
COMA ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
GOUT ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PSYCHIATRIC SYMPTOM ( 3 FDA reports)
PULMONARY CONGESTION ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
FEAR ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 2 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
THIRST ( 2 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTIFICIAL ANUS ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
HEAT ILLNESS ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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