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

PAIN ( 29 FDA reports)
RENAL FAILURE ( 27 FDA reports)
INJURY ( 24 FDA reports)
UNEVALUABLE EVENT ( 24 FDA reports)
ANXIETY ( 22 FDA reports)
FEAR ( 21 FDA reports)
EMOTIONAL DISTRESS ( 20 FDA reports)
RENAL INJURY ( 18 FDA reports)
ANHEDONIA ( 15 FDA reports)
STRESS ( 15 FDA reports)
MULTI-ORGAN FAILURE ( 13 FDA reports)
RENAL IMPAIRMENT ( 13 FDA reports)
CEREBROVASCULAR ACCIDENT ( 12 FDA reports)
DEPRESSION ( 11 FDA reports)
DEATH ( 8 FDA reports)
RENAL FAILURE ACUTE ( 7 FDA reports)
MYOCARDIAL INFARCTION ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
FEAR OF DEATH ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
PHLEBITIS ( 4 FDA reports)
RESPIRATORY DISTRESS ( 4 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
FUNGAEMIA ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
INFUSION SITE THROMBOSIS ( 3 FDA reports)
LOCKED-IN SYNDROME ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
ANAESTHETIC COMPLICATION ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
APNOEA ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BRAIN STEM HAEMORRHAGE ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CEREBROVASCULAR SPASM ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
MYOCLONIC EPILEPSY ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
CARBOXYHAEMOGLOBIN INCREASED ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
POISONING ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TRAUMATIC LIVER INJURY ( 1 FDA reports)
TREMOR ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VICTIM OF HOMICIDE ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use