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

HYPERTENSION ( 35 FDA reports)
RENAL FAILURE ( 33 FDA reports)
ANAEMIA ( 29 FDA reports)
PYREXIA ( 28 FDA reports)
DIARRHOEA ( 23 FDA reports)
HYPERKALAEMIA ( 23 FDA reports)
RENAL IMPAIRMENT ( 22 FDA reports)
CARDIAC FAILURE ( 21 FDA reports)
RENAL FAILURE ACUTE ( 20 FDA reports)
HAEMOGLOBIN DECREASED ( 18 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 18 FDA reports)
PLATELET COUNT DECREASED ( 18 FDA reports)
RENAL FAILURE CHRONIC ( 18 FDA reports)
DECREASED APPETITE ( 17 FDA reports)
THROMBOCYTOPENIA ( 17 FDA reports)
INSOMNIA ( 16 FDA reports)
VOMITING ( 16 FDA reports)
BLOOD PRESSURE DECREASED ( 15 FDA reports)
DELIRIUM ( 15 FDA reports)
PLEURAL EFFUSION ( 15 FDA reports)
COUGH ( 13 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 13 FDA reports)
HYPOTHYROIDISM ( 13 FDA reports)
MALAISE ( 13 FDA reports)
DYSPEPSIA ( 12 FDA reports)
FATIGUE ( 12 FDA reports)
FEBRILE NEUTROPENIA ( 12 FDA reports)
HYPOGLYCAEMIA ( 12 FDA reports)
NAUSEA ( 12 FDA reports)
AGRANULOCYTOSIS ( 11 FDA reports)
CEREBRAL INFARCTION ( 11 FDA reports)
CONSTIPATION ( 11 FDA reports)
DIALYSIS ( 11 FDA reports)
PNEUMONIA ( 11 FDA reports)
SEPSIS ( 11 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 10 FDA reports)
BLOOD CREATININE INCREASED ( 10 FDA reports)
HYPERGLYCAEMIA ( 10 FDA reports)
HYPOALBUMINAEMIA ( 10 FDA reports)
HYPOCALCAEMIA ( 10 FDA reports)
NEUTROPENIA ( 10 FDA reports)
RESPIRATORY FAILURE ( 10 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 9 FDA reports)
DYSPNOEA ( 9 FDA reports)
HYPERURICAEMIA ( 9 FDA reports)
HYPOPHOSPHATAEMIA ( 9 FDA reports)
INTERSTITIAL LUNG DISEASE ( 9 FDA reports)
STOMATITIS ( 9 FDA reports)
COMA ( 8 FDA reports)
CONVULSION ( 8 FDA reports)
DEHYDRATION ( 8 FDA reports)
DIZZINESS ( 8 FDA reports)
HALLUCINATION ( 8 FDA reports)
HYPOKALAEMIA ( 8 FDA reports)
ILEUS ( 8 FDA reports)
NEUTROPHIL COUNT DECREASED ( 8 FDA reports)
RHABDOMYOLYSIS ( 8 FDA reports)
BLOOD POTASSIUM INCREASED ( 7 FDA reports)
BLOOD PRESSURE INCREASED ( 7 FDA reports)
BRADYCARDIA ( 7 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
INFECTION ( 7 FDA reports)
INTESTINAL OBSTRUCTION ( 7 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 7 FDA reports)
RENAL CELL CARCINOMA ( 7 FDA reports)
SKIN ULCER ( 7 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 6 FDA reports)
ARRHYTHMIA ( 6 FDA reports)
ATRIAL FIBRILLATION ( 6 FDA reports)
BLOOD AMYLASE INCREASED ( 6 FDA reports)
DEATH ( 6 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 6 FDA reports)
DRUG ERUPTION ( 6 FDA reports)
DUODENAL ULCER ( 6 FDA reports)
DYSARTHRIA ( 6 FDA reports)
ENCEPHALOPATHY ( 6 FDA reports)
HYPONATRAEMIA ( 6 FDA reports)
LIPASE INCREASED ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
MEMORY IMPAIRMENT ( 6 FDA reports)
RASH ( 6 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 6 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
CHOLANGITIS ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
DISORIENTATION ( 5 FDA reports)
DYSLALIA ( 5 FDA reports)
ENTERITIS INFECTIOUS ( 5 FDA reports)
ENTEROCOLITIS ( 5 FDA reports)
FALL ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
GASTRIC ULCER ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 5 FDA reports)
LIVER DISORDER ( 5 FDA reports)
OVERDOSE ( 5 FDA reports)
SEPTIC SHOCK ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
VISUAL IMPAIRMENT ( 5 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
BLOOD SODIUM DECREASED ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
BLOOD URIC ACID INCREASED ( 4 FDA reports)
BONE MARROW FAILURE ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
HAEMATURIA ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
HYPERAMMONAEMIA ( 4 FDA reports)
OVARIAN CANCER RECURRENT ( 4 FDA reports)
PROTHROMBIN TIME PROLONGED ( 4 FDA reports)
PURPURA ( 4 FDA reports)
RECTAL ULCER ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
SHOCK ( 4 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
X-RAY ABNORMAL ( 4 FDA reports)
AGITATION ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ANTI-INSULIN ANTIBODY INCREASED ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
DIFFICULTY IN WALKING ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
GRANULOCYTOPENIA ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HEMIPLEGIA ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HYPERPHOSPHATAEMIA ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 3 FDA reports)
LOGORRHOEA ( 3 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 3 FDA reports)
METABOLIC ENCEPHALOPATHY ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PROSTATE CANCER STAGE IV ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BILIRUBINURIA ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CEREBELLAR ATAXIA ( 2 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DERMATITIS ACNEIFORM ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 2 FDA reports)
FRACTURE ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 2 FDA reports)
GASTROINTESTINAL OEDEMA ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
INTRACARDIAC THROMBUS ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 2 FDA reports)
LARGE INTESTINE CARCINOMA ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
PHARYNGEAL STENOSIS ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL HAEMATOMA ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SHUNT OCCLUSION ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ACNE ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
ANAL HAEMORRHAGE ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BILIARY TRACT INFECTION ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMAL CYST ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENTEROCOLITIS BACTERIAL ( 1 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GOITRE ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HYPERAMYLASAEMIA ( 1 FDA reports)
HYPERCHLORAEMIA ( 1 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOALDOSTERONISM ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PERIPHERAL NERVE PALSY ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERITONEAL ADHESIONS ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULSE PRESSURE DECREASED ( 1 FDA reports)
PUS IN STOOL ( 1 FDA reports)
PYURIA ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
SHUNT MALFUNCTION ( 1 FDA reports)
SHUNT STENOSIS ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)

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