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

CARDIAC FAILURE ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
TREMOR ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
CRYING ( 3 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
ERUCTATION ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
PSYCHOMOTOR AGITATION ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
VOMITING ( 3 FDA reports)
AGITATION ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
GASTRITIS HAEMORRHAGIC ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT NON-RESECTABLE ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALLANAESTHESIA ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SERUM SEROTONIN INCREASED ( 1 FDA reports)
SKIN MACERATION ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENOSYNOVITIS STENOSANS ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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