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

VOMITING ( 53 FDA reports)
DEHYDRATION ( 42 FDA reports)
DIARRHOEA ( 33 FDA reports)
ABDOMINAL PAIN ( 30 FDA reports)
FATIGUE ( 28 FDA reports)
HYPERTENSION ( 27 FDA reports)
PYREXIA ( 26 FDA reports)
DEATH ( 22 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 20 FDA reports)
CIRCULATORY COLLAPSE ( 18 FDA reports)
ABDOMINAL DISTENSION ( 17 FDA reports)
ENTEROCOLITIS ( 17 FDA reports)
EXTRADURAL ABSCESS ( 17 FDA reports)
ASTHENIA ( 16 FDA reports)
OESOPHAGITIS ( 16 FDA reports)
DYSPNOEA ( 15 FDA reports)
CONSTIPATION ( 14 FDA reports)
HYPONATRAEMIA ( 14 FDA reports)
RENAL FAILURE ACUTE ( 14 FDA reports)
GASTRITIS ( 13 FDA reports)
BACK PAIN ( 12 FDA reports)
BRADYCARDIA ( 12 FDA reports)
CEREBRAL ISCHAEMIA ( 12 FDA reports)
DELIRIUM ( 12 FDA reports)
HEPATIC ENCEPHALOPATHY ( 12 FDA reports)
HYPERKALAEMIA ( 12 FDA reports)
HYPOTENSION ( 12 FDA reports)
HYPOTHYROIDISM ( 12 FDA reports)
NAUSEA ( 12 FDA reports)
THROMBOCYTOPENIA ( 11 FDA reports)
CARDIO-RESPIRATORY ARREST ( 10 FDA reports)
DECREASED APPETITE ( 10 FDA reports)
DISEASE PROGRESSION ( 10 FDA reports)
ENCEPHALOPATHY ( 10 FDA reports)
PULMONARY EMBOLISM ( 10 FDA reports)
ANAEMIA ( 9 FDA reports)
PNEUMONIA ( 9 FDA reports)
SOMNOLENCE ( 9 FDA reports)
CHOLECYSTITIS ( 8 FDA reports)
HYPOVOLAEMIA ( 8 FDA reports)
ILEUS ( 8 FDA reports)
LEUKOPENIA ( 8 FDA reports)
NEUTROPENIA ( 8 FDA reports)
URINARY TRACT INFECTION ( 8 FDA reports)
VAGINAL HAEMORRHAGE ( 8 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 8 FDA reports)
ANGINA PECTORIS ( 7 FDA reports)
ATRIAL FIBRILLATION ( 7 FDA reports)
CHEST PAIN ( 7 FDA reports)
GASTROINTESTINAL PERFORATION ( 7 FDA reports)
HAEMOGLOBIN DECREASED ( 7 FDA reports)
MYOCARDIAL ISCHAEMIA ( 7 FDA reports)
NERVOUS SYSTEM DISORDER ( 7 FDA reports)
OTOSALPINGITIS ( 7 FDA reports)
SEPSIS ( 7 FDA reports)
STOMATITIS ( 7 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 6 FDA reports)
CONFUSIONAL STATE ( 6 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 6 FDA reports)
GINGIVITIS ( 6 FDA reports)
HYPERBILIRUBINAEMIA ( 6 FDA reports)
LIPOMA ( 6 FDA reports)
MENTAL STATUS CHANGES ( 6 FDA reports)
OSTEOMYELITIS ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
RHEUMATOID ARTHRITIS ( 6 FDA reports)
STAPHYLOCOCCAL INFECTION ( 6 FDA reports)
SUBILEUS ( 6 FDA reports)
WEIGHT DECREASED ( 6 FDA reports)
ATAXIA ( 5 FDA reports)
BLOOD CREATININE INCREASED ( 5 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 5 FDA reports)
CYANOSIS ( 5 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 5 FDA reports)
FALL ( 5 FDA reports)
ISCHAEMIA ( 5 FDA reports)
ISCHAEMIC STROKE ( 5 FDA reports)
NEOPLASM MALIGNANT ( 5 FDA reports)
ORTHOSTATIC HYPOTENSION ( 5 FDA reports)
PNEUMOTHORAX ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
VENTRICULAR TACHYCARDIA ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
CHOLANGITIS ( 4 FDA reports)
COGNITIVE DISORDER ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
HAEMATOMA ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
INTESTINAL ISCHAEMIA ( 4 FDA reports)
MALAISE ( 4 FDA reports)
MUSCLE TIGHTNESS ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 4 FDA reports)
POLYCYTHAEMIA ( 4 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 4 FDA reports)
RECTAL HAEMORRHAGE ( 4 FDA reports)
SINUS BRADYCARDIA ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 4 FDA reports)
SUDDEN DEATH ( 4 FDA reports)
THROAT TIGHTNESS ( 4 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 4 FDA reports)
ANXIETY ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
COMA HEPATIC ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
FEMORAL ARTERY OCCLUSION ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
MELAENA ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PERITONITIS BACTERIAL ( 3 FDA reports)
PRESYNCOPE ( 3 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 3 FDA reports)
SMALL INTESTINE ULCER ( 3 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL MASS ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
ANAL INFLAMMATION ( 2 FDA reports)
ANOXIA ( 2 FDA reports)
AORTIC ANEURYSM RUPTURE ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
BACTERIAL SEPSIS ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CANDIDA PNEUMONIA ( 2 FDA reports)
CARDIAC ENZYMES INCREASED ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTESTINAL FISTULA ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
OCULAR ICTERUS ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 2 FDA reports)
RENAL ARTERY DISSECTION ( 2 FDA reports)
RENAL ARTERY OCCLUSION ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC ILEUS ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMOCONCENTRATION ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYOPNEUMOTHORAX ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
SCROTAL OEDEMA ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TUMOUR ASSOCIATED FEVER ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)

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