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

CEREBRAL INFARCTION ( 5 FDA reports)
FOLLICULITIS ( 5 FDA reports)
NASOPHARYNGITIS ( 5 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
LACUNAR INFARCTION ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
ACARODERMATITIS ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLEEDING TIME PROLONGED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
FALL ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
RASH ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
CREATININE URINE INCREASED ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIFFUSE PANBRONCHIOLITIS ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FUNGAL ENDOCARDITIS ( 1 FDA reports)
FUNGAL SEPSIS ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENINGITIS LISTERIA ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYOTHORAX ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL ISCHAEMIA ( 1 FDA reports)
REPERFUSION INJURY ( 1 FDA reports)
RESIDUAL URINE VOLUME ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SCEDOSPORIUM INFECTION ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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