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

DIARRHOEA ( 9 FDA reports)
FALL ( 9 FDA reports)
RENAL FAILURE ( 8 FDA reports)
DRUG INTERACTION ( 7 FDA reports)
FATIGUE ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
TOXIC SKIN ERUPTION ( 6 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
ECZEMA ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
VOMITING ( 5 FDA reports)
ANAEMIA ( 4 FDA reports)
ASCITES ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
AZOTAEMIA ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DIFFICULTY IN WALKING ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
HAEMOLYSIS ( 3 FDA reports)
HAEMOLYTIC ANAEMIA ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HEPATITIS TOXIC ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
JOINT DISLOCATION ( 3 FDA reports)
LACTIC ACIDOSIS ( 3 FDA reports)
MUSCLE CRAMP ( 3 FDA reports)
MYOPATHY ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SENSATION OF HEAVINESS ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
APATHY ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
COLITIS ( 2 FDA reports)
COMA ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DISINHIBITION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 2 FDA reports)
ENCEPHALITIS HERPES ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
FANCONI SYNDROME ( 2 FDA reports)
FEAR ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GASTRIC NEOPLASM ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
NEPHRITIS INTERSTITIAL ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RENAL PAIN ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RETROPERITONEAL FIBROSIS ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
STRESS ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
THROMBOCYTHAEMIA ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TRIGEMINAL NEURALGIA ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ACANTHOMA ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACTINIC KERATOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BENIGN COLONIC POLYP ( 1 FDA reports)
BLADDER CALCULUS REMOVAL ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE 0 ( 1 FDA reports)
BLEEDING VARICOSE VEIN ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
CALCULUS BLADDER ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHOLINERGIC SYNDROME ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR X LEVEL DECREASED ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CYSTIC FIBROSIS PANCREATIC ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
ERYTHRODERMIC PSORIASIS ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING GUILTY ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
FRACTURED COCCYX ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GENITAL PAIN ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT NON-RESECTABLE ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HYPERADRENOCORTICISM ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOPROTHROMBINAEMIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCTOCOLITIS ( 1 FDA reports)
PROTEUS TEST POSITIVE ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PYELONEPHRITIS CHRONIC ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 1 FDA reports)
RETINAL ARTERY EMBOLISM ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SKIN STRIAE ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
VARICOSE VEIN RUPTURED ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WOUND ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use