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

DYSPNOEA ( 18 FDA reports)
DIABETES MELLITUS ( 15 FDA reports)
PNEUMONIA ( 15 FDA reports)
ABDOMINAL PAIN ( 14 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 14 FDA reports)
BACK PAIN ( 13 FDA reports)
SEPSIS ( 13 FDA reports)
WEIGHT DECREASED ( 13 FDA reports)
ASTHENIA ( 12 FDA reports)
BLOOD GLUCOSE INCREASED ( 12 FDA reports)
KERATITIS ( 12 FDA reports)
ULCERATIVE KERATITIS ( 12 FDA reports)
ANAEMIA ( 11 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 10 FDA reports)
RENAL FAILURE ACUTE ( 10 FDA reports)
VISUAL IMPAIRMENT ( 10 FDA reports)
BLOOD CREATININE INCREASED ( 9 FDA reports)
DIZZINESS ( 9 FDA reports)
HIV INFECTION ( 9 FDA reports)
SOMNOLENCE ( 9 FDA reports)
DRUG INTERACTION ( 8 FDA reports)
MUSCULAR WEAKNESS ( 8 FDA reports)
THROMBOCYTOPENIA ( 8 FDA reports)
DEATH ( 7 FDA reports)
DIARRHOEA ( 7 FDA reports)
GASTRIC HAEMORRHAGE ( 7 FDA reports)
GASTRIC ULCER ( 7 FDA reports)
HAEMATEMESIS ( 7 FDA reports)
HELICOBACTER TEST POSITIVE ( 7 FDA reports)
INFECTION ( 7 FDA reports)
MYOCARDIAL INFARCTION ( 7 FDA reports)
OEDEMA ( 7 FDA reports)
PULMONARY OEDEMA ( 7 FDA reports)
URINARY TRACT INFECTION ( 7 FDA reports)
VOMITING ( 7 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 6 FDA reports)
BALANCE DISORDER ( 6 FDA reports)
BRADYCARDIA ( 6 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 6 FDA reports)
COAGULOPATHY ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
HEART RATE IRREGULAR ( 6 FDA reports)
HYPERGLYCAEMIA ( 6 FDA reports)
JOINT STIFFNESS ( 6 FDA reports)
LIPASE INCREASED ( 6 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 6 FDA reports)
MOBILITY DECREASED ( 6 FDA reports)
MOUTH HAEMORRHAGE ( 6 FDA reports)
NEUROPATHY PERIPHERAL ( 6 FDA reports)
NEUTROPENIA ( 6 FDA reports)
PIGMENTATION DISORDER ( 6 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 6 FDA reports)
RENAL IMPAIRMENT ( 6 FDA reports)
VARICOSE VEIN ( 6 FDA reports)
BACTERAEMIA ( 5 FDA reports)
CARDIAC FAILURE ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
HAEMOGLOBIN ( 5 FDA reports)
HYPERURICAEMIA ( 5 FDA reports)
HYPOACUSIS ( 5 FDA reports)
MELAENA ( 5 FDA reports)
PAIN ( 5 FDA reports)
PULMONARY CONGESTION ( 5 FDA reports)
TRANSPLANT REJECTION ( 5 FDA reports)
WOUND ( 5 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 4 FDA reports)
COLITIS ( 4 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 4 FDA reports)
HAEMODYNAMIC INSTABILITY ( 4 FDA reports)
JAUNDICE ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
MUCOSAL INFLAMMATION ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
PARKINSONISM ( 4 FDA reports)
POLYDIPSIA ( 4 FDA reports)
PYELONEPHRITIS ( 4 FDA reports)
TOOTH LOSS ( 4 FDA reports)
URETERAL STENT INSERTION ( 4 FDA reports)
BILE DUCT STENOSIS ( 3 FDA reports)
BILIARY ISCHAEMIA ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
LEFT VENTRICULAR FAILURE ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
SHOCK HYPOGLYCAEMIC ( 3 FDA reports)
SUPERINFECTION ( 3 FDA reports)
SWELLING ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABDOMINAL HERNIA ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ARTERIAL CATHETERISATION ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ASCITES ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BRONCHITIS ACUTE ( 2 FDA reports)
BRONCHITIS CHRONIC ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC FAILURE CHRONIC ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CATARACT SUBCAPSULAR ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
ENTEROCOLITIS BACTERIAL ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTROSTOMY TUBE INSERTION ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
INTESTINAL PROLAPSE ( 2 FDA reports)
LARYNGITIS ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LYMPHOCELE ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
NEPHROANGIOSCLEROSIS ( 2 FDA reports)
NEPHROGENIC ANAEMIA ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SUTURE RUPTURE ( 2 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ALCOHOLIC PSYCHOSIS ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CAUDA EQUINA SYNDROME ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DEVICE MIGRATION ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
FALL ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GROIN ABSCESS ( 1 FDA reports)
GROUP B STREPTOCOCCUS NEONATAL SEPSIS ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS ALCOHOLIC ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE THROMBOSIS ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL OPERATION ( 1 FDA reports)
JAW OPERATION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIPODYSTROPHY ACQUIRED ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
ROTAVIRUS TEST POSITIVE ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TUBO-OVARIAN ABSCESS ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
ULCER ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URTICARIA PAPULAR ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use