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

GASTROINTESTINAL HAEMORRHAGE ( 9 FDA reports)
DRUG INTERACTION ( 7 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
OESOPHAGEAL ULCER ( 5 FDA reports)
FALL ( 4 FDA reports)
REFLUX OESOPHAGITIS ( 4 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
HAEMOLYSIS ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
CHOREA ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DIVERTICULAR PERFORATION ( 2 FDA reports)
DUODENAL ULCER PERFORATION ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
METABOLIC ALKALOSIS ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GOITRE ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HORNER'S SYNDROME ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERSEXUALITY ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MELAENA ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PELVIC FLOOR REPAIR ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL HYPERTENSION ( 1 FDA reports)
RENAL ISCHAEMIA ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPONDYLITIS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use