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

VOMITING ( 126 FDA reports)
ANAEMIA ( 107 FDA reports)
DEHYDRATION ( 82 FDA reports)
DYSPNOEA ( 73 FDA reports)
HYPOKALAEMIA ( 67 FDA reports)
DECREASED APPETITE ( 66 FDA reports)
PULMONARY EMBOLISM ( 65 FDA reports)
DISEASE PROGRESSION ( 63 FDA reports)
PYREXIA ( 62 FDA reports)
NAUSEA ( 57 FDA reports)
DIARRHOEA ( 52 FDA reports)
FATIGUE ( 52 FDA reports)
BACK PAIN ( 49 FDA reports)
PNEUMONIA ( 43 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 39 FDA reports)
BONE PAIN ( 38 FDA reports)
PLEURAL EFFUSION ( 38 FDA reports)
PROSTATE CANCER ( 36 FDA reports)
BREAST CANCER METASTATIC ( 35 FDA reports)
HYPOTENSION ( 35 FDA reports)
LETHARGY ( 34 FDA reports)
SEPSIS ( 33 FDA reports)
RENAL FAILURE ( 32 FDA reports)
PROSTATE CANCER METASTATIC ( 31 FDA reports)
THROMBOCYTOPENIA ( 31 FDA reports)
URINARY TRACT INFECTION ( 29 FDA reports)
ASTHENIA ( 28 FDA reports)
CONFUSIONAL STATE ( 28 FDA reports)
DEEP VEIN THROMBOSIS ( 28 FDA reports)
DEATH ( 27 FDA reports)
MUSCULAR WEAKNESS ( 27 FDA reports)
JAUNDICE ( 26 FDA reports)
PAIN ( 26 FDA reports)
RENAL FAILURE ACUTE ( 25 FDA reports)
DRUG INEFFECTIVE ( 23 FDA reports)
HAEMATURIA ( 23 FDA reports)
CONSTIPATION ( 22 FDA reports)
HYPERURICAEMIA ( 22 FDA reports)
HYPERKALAEMIA ( 21 FDA reports)
ABDOMINAL PAIN ( 20 FDA reports)
ATRIAL FIBRILLATION ( 20 FDA reports)
DRUG INTERACTION ( 20 FDA reports)
FEBRILE NEUTROPENIA ( 20 FDA reports)
MALAISE ( 20 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 20 FDA reports)
SPINAL FRACTURE ( 20 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 19 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 18 FDA reports)
GASTROENTERITIS ( 18 FDA reports)
LIPASE INCREASED ( 18 FDA reports)
LUNG INFECTION ( 18 FDA reports)
BLOOD CREATININE INCREASED ( 17 FDA reports)
PANCREATITIS ACUTE ( 17 FDA reports)
RHABDOMYOLYSIS ( 17 FDA reports)
ABDOMINAL PAIN UPPER ( 16 FDA reports)
DIZZINESS ( 16 FDA reports)
HEPATIC ENZYME INCREASED ( 16 FDA reports)
NERVE ROOT COMPRESSION ( 16 FDA reports)
PNEUMOTHORAX ( 16 FDA reports)
ANGINA UNSTABLE ( 15 FDA reports)
BLOOD URIC ACID INCREASED ( 14 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 14 FDA reports)
NEOPLASM PROGRESSION ( 14 FDA reports)
PNEUMONITIS ( 14 FDA reports)
PANCYTOPENIA ( 13 FDA reports)
PLATELET COUNT DECREASED ( 13 FDA reports)
RESPIRATORY FAILURE ( 13 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 13 FDA reports)
FAILURE TO THRIVE ( 12 FDA reports)
OEDEMA PERIPHERAL ( 12 FDA reports)
UROSEPSIS ( 12 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 12 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 11 FDA reports)
URINARY RETENTION ( 11 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 10 FDA reports)
CEREBRAL ISCHAEMIA ( 10 FDA reports)
CHEST DISCOMFORT ( 10 FDA reports)
HEADACHE ( 10 FDA reports)
HEPATITIS ( 10 FDA reports)
HYPOGLYCAEMIA ( 10 FDA reports)
HYPOPHOSPHATAEMIA ( 10 FDA reports)
OSTEOSCLEROSIS ( 10 FDA reports)
SEPTIC SHOCK ( 10 FDA reports)
TUMOUR FLARE ( 10 FDA reports)
COORDINATION ABNORMAL ( 9 FDA reports)
ERYTHEMA MULTIFORME ( 9 FDA reports)
HYPONATRAEMIA ( 9 FDA reports)
SPINAL CORD COMPRESSION ( 9 FDA reports)
ARTHRALGIA ( 8 FDA reports)
CEREBROVASCULAR ACCIDENT ( 8 FDA reports)
DRUG ADMINISTRATION ERROR ( 8 FDA reports)
DRUG-INDUCED LIVER INJURY ( 8 FDA reports)
HAEMOGLOBIN DECREASED ( 8 FDA reports)
HEMIPARESIS ( 8 FDA reports)
HYPERTENSION ( 8 FDA reports)
MYOCARDIAL INFARCTION ( 8 FDA reports)
NEUTROPENIA ( 8 FDA reports)
PAIN IN EXTREMITY ( 8 FDA reports)
RASH ( 8 FDA reports)
RECTAL HAEMORRHAGE ( 8 FDA reports)
RETINAL ISCHAEMIA ( 8 FDA reports)
SUDDEN DEATH ( 8 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 8 FDA reports)
TUMOUR PAIN ( 8 FDA reports)
VASCULITIS ( 8 FDA reports)
CHEST PAIN ( 7 FDA reports)
MUSCULOSKELETAL PAIN ( 7 FDA reports)
ACUTE CORONARY SYNDROME ( 6 FDA reports)
ACUTE RESPIRATORY FAILURE ( 6 FDA reports)
AGITATION ( 6 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 6 FDA reports)
CARDIAC ARREST ( 6 FDA reports)
CARDIAC FAILURE ( 6 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 6 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 6 FDA reports)
DYSURIA ( 6 FDA reports)
ELECTROLYTE IMBALANCE ( 6 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 6 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 6 FDA reports)
GROIN PAIN ( 6 FDA reports)
HEPATIC FAILURE ( 6 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 6 FDA reports)
MEMORY IMPAIRMENT ( 6 FDA reports)
MYOCARDIAL ISCHAEMIA ( 6 FDA reports)
PULMONARY OEDEMA ( 6 FDA reports)
RESPIRATORY DISTRESS ( 6 FDA reports)
SOMNOLENCE ( 6 FDA reports)
STAPHYLOCOCCAL INFECTION ( 6 FDA reports)
STEVENS-JOHNSON SYNDROME ( 6 FDA reports)
SUICIDAL IDEATION ( 6 FDA reports)
TACHYCARDIA ( 6 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 6 FDA reports)
AMNESIA ( 5 FDA reports)
BRADYKINESIA ( 5 FDA reports)
DIZZINESS EXERTIONAL ( 5 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 5 FDA reports)
METASTASES TO LIVER ( 5 FDA reports)
MUSCLE RIGIDITY ( 5 FDA reports)
ABASIA ( 4 FDA reports)
ABDOMINAL PAIN LOWER ( 4 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 4 FDA reports)
ARTHRITIS BACTERIAL ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
COMA ( 4 FDA reports)
CONCUSSION ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 4 FDA reports)
DERMATITIS BULLOUS ( 4 FDA reports)
DEVICE LEAKAGE ( 4 FDA reports)
DISTURBANCE IN ATTENTION ( 4 FDA reports)
DRUG DOSE OMISSION ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
EASTERN COOPERATIVE ONCOLOGY GROUP PERFORMANCE STATUS WORSENED ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
FALL ( 4 FDA reports)
FEELING COLD ( 4 FDA reports)
GASTROENTERITIS VIRAL ( 4 FDA reports)
GASTROINTESTINAL INFECTION ( 4 FDA reports)
HAEMATOMA ( 4 FDA reports)
HEPATITIS TOXIC ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
HYPOALDOSTERONISM ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
INTESTINAL ISCHAEMIA ( 4 FDA reports)
LONG QT SYNDROME ( 4 FDA reports)
LYMPHOPENIA ( 4 FDA reports)
METASTASES TO BONE ( 4 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 4 FDA reports)
METASTASES TO SPINE ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
MYELODYSPLASTIC SYNDROME ( 4 FDA reports)
MYOPATHY ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
PARAPARESIS ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 4 FDA reports)
SOFT TISSUE INFECTION ( 4 FDA reports)
SPONDYLOLISTHESIS ( 4 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 4 FDA reports)
SUBDURAL HAEMORRHAGE ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
TRANSAMINASES INCREASED ( 4 FDA reports)
VENOUS THROMBOSIS ( 4 FDA reports)
ACUTE HEPATIC FAILURE ( 3 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
OSTEOPOROTIC FRACTURE ( 3 FDA reports)
STRESS FRACTURE ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 2 FDA reports)
AORTIC STENOSIS ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
B-CELL TYPE ACUTE LEUKAEMIA ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
CANCER PAIN ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CHRONIC HEPATIC FAILURE ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CREPITATIONS ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 2 FDA reports)
ESCHERICHIA TEST POSITIVE ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROINTESTINAL NECROSIS ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 2 FDA reports)
INFECTED SKIN ULCER ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INFECTIOUS PERITONITIS ( 2 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
INGUINAL HERNIA STRANGULATED ( 2 FDA reports)
INTESTINAL INFARCTION ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
MANIA ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
MYASTHENIA GRAVIS ( 2 FDA reports)
NEPHRECTOMY ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 2 FDA reports)
PATHOLOGICAL FRACTURE ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 2 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPINAL COLUMN STENOSIS ( 2 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
TACHYARRHYTHMIA ( 2 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
URETERIC STENOSIS ( 2 FDA reports)
URETHRAL STENOSIS ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
WOUND COMPLICATION ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RETCHING ( 1 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 1 FDA reports)
URTICARIA ( 1 FDA reports)

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