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

CONDITION AGGRAVATED ( 78 FDA reports)
CARDIAC FAILURE ( 68 FDA reports)
INTERSTITIAL LUNG DISEASE ( 62 FDA reports)
PNEUMONIA ( 42 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 41 FDA reports)
MULTI-ORGAN FAILURE ( 41 FDA reports)
LUNG DISORDER ( 36 FDA reports)
VENTRICULAR TACHYCARDIA ( 35 FDA reports)
JAUNDICE ( 32 FDA reports)
DEATH ( 30 FDA reports)
BLOOD PRESSURE DECREASED ( 27 FDA reports)
ANAEMIA ( 26 FDA reports)
VENTRICULAR FIBRILLATION ( 26 FDA reports)
HEPATIC FAILURE ( 25 FDA reports)
DECREASED APPETITE ( 24 FDA reports)
ATRIAL FIBRILLATION ( 23 FDA reports)
PHLEBITIS ( 23 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 23 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 22 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 21 FDA reports)
BRADYCARDIA ( 21 FDA reports)
DRUG INEFFECTIVE ( 21 FDA reports)
BLOOD BILIRUBIN INCREASED ( 20 FDA reports)
LIVER DISORDER ( 20 FDA reports)
PNEUMONIA BACTERIAL ( 20 FDA reports)
RENAL FAILURE ( 20 FDA reports)
AGRANULOCYTOSIS ( 18 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 17 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 16 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 16 FDA reports)
THROMBOCYTOPENIA ( 16 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 15 FDA reports)
OEDEMA PERIPHERAL ( 15 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 15 FDA reports)
CARDIAC FAILURE CHRONIC ( 14 FDA reports)
RENAL IMPAIRMENT ( 14 FDA reports)
HEPATITIS FULMINANT ( 13 FDA reports)
NAUSEA ( 13 FDA reports)
VOMITING ( 13 FDA reports)
CARDIAC FAILURE ACUTE ( 12 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 12 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 12 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 12 FDA reports)
HYPOTHYROIDISM ( 12 FDA reports)
PLEURAL EFFUSION ( 12 FDA reports)
RESPIRATORY FAILURE ( 12 FDA reports)
BLOOD UREA INCREASED ( 11 FDA reports)
CARDIAC ARREST ( 11 FDA reports)
SHOCK ( 11 FDA reports)
ABDOMINAL PAIN ( 10 FDA reports)
MALAISE ( 10 FDA reports)
OESOPHAGEAL ULCER ( 10 FDA reports)
WEIGHT INCREASED ( 10 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 10 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 9 FDA reports)
DRUG EFFECT DECREASED ( 9 FDA reports)
GASTRIC ULCER ( 9 FDA reports)
HYPOGLYCAEMIA ( 9 FDA reports)
OEDEMA ( 9 FDA reports)
SEPSIS ( 9 FDA reports)
ARTHRALGIA ( 8 FDA reports)
ASTHENIA ( 8 FDA reports)
CHILLS ( 8 FDA reports)
DEHYDRATION ( 8 FDA reports)
DYSURIA ( 8 FDA reports)
FACE OEDEMA ( 8 FDA reports)
HEADACHE ( 8 FDA reports)
HYPERTHYROIDISM ( 8 FDA reports)
PYELONEPHRITIS ACUTE ( 8 FDA reports)
PYREXIA ( 8 FDA reports)
URINARY TRACT INFECTION ( 8 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 7 FDA reports)
BLOOD SODIUM DECREASED ( 7 FDA reports)
CARDIO-RESPIRATORY ARREST ( 7 FDA reports)
CEREBRAL INFARCTION ( 7 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 7 FDA reports)
GASTRIC NEOPLASM ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
OESOPHAGEAL NEOPLASM ( 7 FDA reports)
PROTEIN TOTAL DECREASED ( 7 FDA reports)
RENAL FAILURE ACUTE ( 7 FDA reports)
SICK SINUS SYNDROME ( 7 FDA reports)
STREPTOCOCCAL INFECTION ( 7 FDA reports)
THYROIDITIS ( 7 FDA reports)
ALOPECIA ( 6 FDA reports)
ANOREXIA ( 6 FDA reports)
ASCITES ( 6 FDA reports)
BLOOD ALBUMIN DECREASED ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
CARDIOGENIC SHOCK ( 6 FDA reports)
COUGH ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
HAEMATOCRIT DECREASED ( 6 FDA reports)
HEPATIC ENZYME INCREASED ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 6 FDA reports)
INFECTION ( 6 FDA reports)
OFF LABEL USE ( 6 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 6 FDA reports)
PLATELET COUNT DECREASED ( 6 FDA reports)
PNEUMONIA FUNGAL ( 6 FDA reports)
PNEUMONIA VIRAL ( 6 FDA reports)
THROMBOSIS IN DEVICE ( 6 FDA reports)
ANAPHYLACTIC SHOCK ( 5 FDA reports)
ASTHMA ( 5 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 5 FDA reports)
CELL MARKER INCREASED ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
DYSPNOEA EXERTIONAL ( 5 FDA reports)
EJECTION FRACTION DECREASED ( 5 FDA reports)
ENDOTRACHEAL INTUBATION ( 5 FDA reports)
FUNGAL INFECTION ( 5 FDA reports)
GENERALISED OEDEMA ( 5 FDA reports)
HYPERNATRAEMIA ( 5 FDA reports)
LUPUS-LIKE SYNDROME ( 5 FDA reports)
ORTHOPNOEA ( 5 FDA reports)
PANCREATIC ENZYME ABNORMALITY ( 5 FDA reports)
PULMONARY OEDEMA ( 5 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 5 FDA reports)
RENAL CELL CARCINOMA ( 5 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 4 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 4 FDA reports)
BONE MARROW FAILURE ( 4 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 4 FDA reports)
CARDIOMEGALY ( 4 FDA reports)
GRANULOCYTOPENIA ( 4 FDA reports)
KLEBSIELLA INFECTION ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
LIVER INJURY ( 4 FDA reports)
LONG QT SYNDROME ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PNEUMONIA ASPIRATION ( 4 FDA reports)
POST PROCEDURAL HAEMATOMA ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
SINUS ARREST ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
SUDDEN CARDIAC DEATH ( 4 FDA reports)
ACIDOSIS ( 3 FDA reports)
ASPERGILLOSIS ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HYPERBILIRUBINAEMIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 3 FDA reports)
OESOPHAGEAL CARCINOMA ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
SERRATIA INFECTION ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
TORSADE DE POINTES ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 3 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BRONCHIECTASIS ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATOCELLULAR INJURY ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
MORAXELLA INFECTION ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
NOCTURNAL DYSPNOEA ( 2 FDA reports)
NODAL RHYTHM ( 2 FDA reports)
OPPORTUNISTIC INFECTION ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PNEUMATOSIS INTESTINALIS ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ACUTE LUNG INJURY ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEFIBRILLATION THRESHOLD INCREASED ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
ENDOCARDITIS CANDIDA ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GOITRE ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIVER SCAN ABNORMAL ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POSTRENAL FAILURE ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
THYROTOXIC CRISIS ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)

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