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

DRUG INTERACTION ( 13 FDA reports)
DIARRHOEA ( 9 FDA reports)
OEDEMA PERIPHERAL ( 8 FDA reports)
PYREXIA ( 7 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
HYPOGLYCAEMIA ( 6 FDA reports)
LEUKOPENIA ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
NEUTROPENIA ( 6 FDA reports)
DRY SKIN ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
MALAISE ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
SKIN FISSURES ( 5 FDA reports)
VENOUS THROMBOSIS LIMB ( 5 FDA reports)
ANAEMIA ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ASCITES ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DIFFICULTY IN WALKING ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
LEG AMPUTATION ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
UTERINE PROLAPSE ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ACHOLIA ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
APATHY ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BIOPSY BONE MARROW ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHOLURIA ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEATH ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIABETIC NEUROPATHY ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PERNICIOUS ANAEMIA ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPUTUM DISCOLOURED ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BRONCHIAL CARCINOMA ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
COLITIS PSEUDOMEMBRANOUS ( 1 FDA reports)
COMA ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FALL ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GASTRIC ULCER HELICOBACTER ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
MUSCLE RUPTURE ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RECTAL ULCER ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
VEIN PAIN ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VOCAL CORD NEOPLASM ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use