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

NAUSEA ( 20 FDA reports)
DIARRHOEA ( 17 FDA reports)
VOMITING ( 14 FDA reports)
DEHYDRATION ( 13 FDA reports)
ABDOMINAL PAIN ( 11 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
ASTHENIA ( 10 FDA reports)
DYSPNOEA ( 10 FDA reports)
PANCYTOPENIA ( 10 FDA reports)
PYREXIA ( 10 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
HAEMOGLOBIN DECREASED ( 9 FDA reports)
PLEURAL EFFUSION ( 9 FDA reports)
DIZZINESS ( 8 FDA reports)
HYPOTENSION ( 8 FDA reports)
HAEMATOCRIT DECREASED ( 7 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 7 FDA reports)
ANAEMIA ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
FEBRILE NEUTROPENIA ( 6 FDA reports)
MULTI-ORGAN FAILURE ( 6 FDA reports)
RASH ( 6 FDA reports)
SEPSIS ( 6 FDA reports)
ASCITES ( 5 FDA reports)
BACK PAIN ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
COMA ( 5 FDA reports)
HYPOKALAEMIA ( 5 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
PLATELET COUNT INCREASED ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
VOMITING PROJECTILE ( 5 FDA reports)
ANOREXIA ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 4 FDA reports)
PROTHROMBIN TIME PROLONGED ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
AGITATION ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPERNATRAEMIA ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
TOOTH EXTRACTION ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
APNOEA ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
ATHEROSCLEROSIS ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHILLS ( 2 FDA reports)
COLON CANCER METASTATIC ( 2 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 2 FDA reports)
ENTERITIS ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
MESOTHELIOMA MALIGNANT ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
OSTEOMYELITIS ACUTE ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
SPUTUM CULTURE POSITIVE ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BASE EXCESS POSITIVE ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE DEBRIDEMENT ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BREAST CELLULITIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CLOSTRIDIUM BACTERAEMIA ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLON CANCER STAGE IV ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
ECTROPION ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FALL ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INCISIONAL HERNIA ( 1 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL SURGERY ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
OSTEOLYSIS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
POST PROCEDURAL DIARRHOEA ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
RADIATION SKIN INJURY ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SURGERY ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITH NERVE PARALYSIS ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)

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