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

DRUG INTERACTION ( 38 FDA reports)
PANCYTOPENIA ( 38 FDA reports)
BACTERIAL SEPSIS ( 26 FDA reports)
SEPSIS ( 23 FDA reports)
FEELING ABNORMAL ( 15 FDA reports)
DRUG LEVEL INCREASED ( 14 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 14 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 14 FDA reports)
PNEUMONIA ( 12 FDA reports)
RENAL FAILURE ACUTE ( 12 FDA reports)
DYSPNOEA ( 11 FDA reports)
NAUSEA ( 11 FDA reports)
PLATELET COUNT DECREASED ( 11 FDA reports)
VOMITING ( 11 FDA reports)
GROIN ABSCESS ( 10 FDA reports)
NEUTROPENIA ( 10 FDA reports)
PYREXIA ( 10 FDA reports)
BURKITT'S LYMPHOMA ( 8 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 8 FDA reports)
LYMPHOCYTOSIS ( 8 FDA reports)
OESOPHAGITIS ULCERATIVE ( 8 FDA reports)
SEPTIC SHOCK ( 8 FDA reports)
TENDONITIS ( 8 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 7 FDA reports)
BLOOD CULTURE POSITIVE ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
CONFUSIONAL STATE ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
APHASIA ( 5 FDA reports)
CHEST DISCOMFORT ( 5 FDA reports)
CHILLS ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
EJECTION FRACTION DECREASED ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
LETHARGY ( 5 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 5 FDA reports)
STREPTOCOCCAL INFECTION ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
EROSIVE OESOPHAGITIS ( 4 FDA reports)
ESCHERICHIA SEPSIS ( 4 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
RECTAL HAEMORRHAGE ( 4 FDA reports)
SINUS TACHYCARDIA ( 4 FDA reports)
SUBDURAL HAEMATOMA ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
TROPONIN INCREASED ( 4 FDA reports)
ACIDOSIS ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ARTERIOSCLEROSIS ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
COMA ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DIVERTICULUM ( 3 FDA reports)
EJACULATION DISORDER ( 3 FDA reports)
EPIDIDYMITIS ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INTRACARDIAC THROMBUS ( 3 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
ORCHITIS ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
RECTAL FISSURE ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
TESTICULAR PAIN ( 3 FDA reports)
TESTICULAR SWELLING ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
VENTRICULAR ARRHYTHMIA ( 3 FDA reports)
VENTRICULAR HYPOKINESIA ( 3 FDA reports)
ANAEMIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ASPIRATION PLEURAL CAVITY ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD CREATINE ABNORMAL ( 2 FDA reports)
BLOOD MAGNESIUM INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
HYDROCELE ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
PAIN ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
SKIN HYPERTROPHY ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
SPUTUM DISCOLOURED ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SYSTEMIC SCLEROSIS ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADHESION ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE LESION ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLOSED FRACTURE MANIPULATION ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLON INJURY ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FALL ( 1 FDA reports)
FIBROSARCOMA ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMOPHILUS SEPSIS ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
IRITIS ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIPOATROPHY ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)

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