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

RENAL FAILURE ACUTE ( 13 FDA reports)
RENAL FAILURE ( 12 FDA reports)
BLOOD CREATININE INCREASED ( 11 FDA reports)
PRURITUS ( 10 FDA reports)
PYREXIA ( 10 FDA reports)
ASTHENIA ( 8 FDA reports)
DIARRHOEA ( 8 FDA reports)
FALL ( 8 FDA reports)
CHROMATURIA ( 7 FDA reports)
COGNITIVE DISORDER ( 7 FDA reports)
HAEMOGLOBIN DECREASED ( 7 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
ANOREXIA ( 6 FDA reports)
HEPATITIS CHOLESTATIC ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
LEUKOCYTOSIS ( 6 FDA reports)
RASH PUSTULAR ( 6 FDA reports)
TOXIC SKIN ERUPTION ( 6 FDA reports)
VISION BLURRED ( 6 FDA reports)
VOMITING ( 6 FDA reports)
DYSPNOEA ( 5 FDA reports)
HEPATOMEGALY ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
NEUTROPHIL COUNT INCREASED ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
OSTEONECROSIS ( 5 FDA reports)
PAIN ( 5 FDA reports)
PANCREATITIS ACUTE ( 5 FDA reports)
PUSTULAR PSORIASIS ( 5 FDA reports)
RASH ERYTHEMATOUS ( 5 FDA reports)
SUDDEN DEATH ( 5 FDA reports)
VISUAL ACUITY REDUCED ( 5 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 4 FDA reports)
BRAIN HERNIATION ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
COUGH ( 4 FDA reports)
CYTOLYTIC HEPATITIS ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 4 FDA reports)
FAECES DISCOLOURED ( 4 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
HEPATIC FIBROSIS ( 4 FDA reports)
JAUNDICE ( 4 FDA reports)
MITRAL VALVE DISEASE ( 4 FDA reports)
MITRAL VALVE INCOMPETENCE ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
RASH MACULO-PAPULAR ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
SKIN REACTION ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
SPUTUM DISCOLOURED ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ANURIA ( 3 FDA reports)
APHASIA ( 3 FDA reports)
ASCITES ( 3 FDA reports)
BONE FISSURE ( 3 FDA reports)
BONE LESION ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
DENTAL IMPLANTATION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
MYDRIASIS ( 3 FDA reports)
PANCREATITIS NECROTISING ( 3 FDA reports)
PRIMARY SEQUESTRUM ( 3 FDA reports)
STOMATITIS NECROTISING ( 3 FDA reports)
TOOTH EXTRACTION ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
ATRIAL THROMBOSIS ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BILE DUCT CANCER ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CEREBELLAR HAEMATOMA ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FOREIGN BODY ( 2 FDA reports)
FOREIGN BODY ASPIRATION ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GLOSSITIS ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEART TRANSPLANT REJECTION ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATOJUGULAR REFLUX ( 2 FDA reports)
HIGH FREQUENCY ABLATION ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PEMPHIGOID ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RENAL COLIC ( 2 FDA reports)
RETINAL ARTERY OCCLUSION ( 2 FDA reports)
RETROPERITONEAL HAEMATOMA ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
RIGHT ATRIAL DILATATION ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
TREMOR ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VENOUS INSUFFICIENCY ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACCOMMODATION DISORDER ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
AORTIC BRUIT ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APATHY ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
AUTOIMMUNE PANCYTOPENIA ( 1 FDA reports)
BICYTOPENIA ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COMA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENTEROCOLONIC FISTULA ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLAMMATORY PAIN ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRACRANIAL HAEMATOMA ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PELVIC FLUID COLLECTION ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
RASH ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
SEIZURE ANOXIC ( 1 FDA reports)
SEQUESTRECTOMY ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STENOTROPHOMONAS SEPSIS ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TENDON OPERATION ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TONGUE CANCER METASTATIC ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VENTRICULAR FAILURE ( 1 FDA reports)
VITREOUS OPACITIES ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use