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

HYPOKALAEMIA ( 8 FDA reports)
HYPOTENSION ( 4 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BRAIN HERNIATION ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BREATH ODOUR ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CRYPTOCOCCOSIS ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 2 FDA reports)
NEUROLOGICAL SYMPTOM ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CAUDA EQUINA SYNDROME ( 1 FDA reports)
CEREBRAL FUNGAL INFECTION ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
COR PULMONALE ACUTE ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
DEATH ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
RALES ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETCHING ( 1 FDA reports)
SENSORIMOTOR DISORDER ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
VASCULITIS CEREBRAL ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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