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CONDITION AGGRAVATED ( 7 FDA reports)
CARDIAC FAILURE ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
CARDIAC FAILURE ACUTE ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 3 FDA reports)
HEPATIC ENCEPHALOPATHY ( 3 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PULMONARY TUBERCULOSIS ( 3 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ARTHRITIS BACTERIAL ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
DYSPHORIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
OSTEOMYELITIS BACTERIAL ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
TONIC CONVULSION ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 1 FDA reports)
FALL ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FUNGAL ENDOCARDITIS ( 1 FDA reports)
FUNGAL SEPSIS ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IRON BINDING CAPACITY UNSATURATED DECREASED ( 1 FDA reports)
JOINT CONTRACTURE ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENINGITIS LISTERIA ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OVARIAN GERM CELL TERATOMA BENIGN ( 1 FDA reports)
PAIN ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PLACENTAL INSUFFICIENCY ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SCEDOSPORIUM INFECTION ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SHUNT OCCLUSION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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