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

BLOOD POTASSIUM DECREASED ( 12 FDA reports)
DIZZINESS POSTURAL ( 12 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 12 FDA reports)
PALPITATIONS ( 12 FDA reports)
LIVER DISORDER ( 7 FDA reports)
NAUSEA ( 7 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
HYPERTHERMIA ( 5 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
ILEUS ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
PNEUMONIA ASPIRATION ( 4 FDA reports)
STEVENS-JOHNSON SYNDROME ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
ANOREXIA NERVOSA ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 3 FDA reports)
DYSPHORIA ( 3 FDA reports)
GASTROINTESTINAL ULCER ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
MALAISE ( 3 FDA reports)
PARKINSONISM ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ANORECTAL OPERATION ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BRONCHIAL HAEMORRHAGE ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COUGH ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
FIBRINOLYSIS INCREASED ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
MELAENA ( 2 FDA reports)
PAIN ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COMA ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DEATH ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RED BLOOD CELL ANISOCYTES PRESENT ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)

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