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

PAIN ( 315 FDA reports)
ANXIETY ( 292 FDA reports)
INJURY ( 289 FDA reports)
RENAL FAILURE ( 272 FDA reports)
UNEVALUABLE EVENT ( 257 FDA reports)
FEAR ( 249 FDA reports)
RENAL INJURY ( 246 FDA reports)
EMOTIONAL DISTRESS ( 233 FDA reports)
ANHEDONIA ( 204 FDA reports)
RENAL IMPAIRMENT ( 188 FDA reports)
STRESS ( 186 FDA reports)
DEATH ( 182 FDA reports)
MULTI-ORGAN FAILURE ( 182 FDA reports)
DEPRESSION ( 96 FDA reports)
THROMBOCYTOPENIA ( 57 FDA reports)
ANAEMIA ( 55 FDA reports)
HYPOTENSION ( 50 FDA reports)
MEDICATION ERROR ( 50 FDA reports)
MYOCARDIAL INFARCTION ( 45 FDA reports)
RENAL FAILURE ACUTE ( 42 FDA reports)
PLATELET COUNT DECREASED ( 40 FDA reports)
CEREBROVASCULAR ACCIDENT ( 39 FDA reports)
HAEMORRHAGE ( 39 FDA reports)
DRUG INEFFECTIVE ( 37 FDA reports)
PYREXIA ( 37 FDA reports)
DYSPNOEA ( 34 FDA reports)
DISABILITY ( 33 FDA reports)
DRUG DISPENSING ERROR ( 33 FDA reports)
MYELODYSPLASTIC SYNDROME ( 32 FDA reports)
PNEUMONIA ( 31 FDA reports)
WEIGHT DECREASED ( 29 FDA reports)
EPISTAXIS ( 28 FDA reports)
NAUSEA ( 28 FDA reports)
DIZZINESS ( 27 FDA reports)
ASTHENIA ( 26 FDA reports)
NERVOUSNESS ( 26 FDA reports)
OEDEMA PERIPHERAL ( 26 FDA reports)
PLEURAL EFFUSION ( 25 FDA reports)
FEAR OF DEATH ( 24 FDA reports)
FATIGUE ( 22 FDA reports)
SPINAL OSTEOARTHRITIS ( 22 FDA reports)
BACK PAIN ( 21 FDA reports)
ABSCESS JAW ( 20 FDA reports)
BACK DISORDER ( 20 FDA reports)
TACHYCARDIA ( 20 FDA reports)
TOOTH EXTRACTION ( 20 FDA reports)
ARTHRALGIA ( 19 FDA reports)
CARDIAC DISORDER ( 19 FDA reports)
HEADACHE ( 19 FDA reports)
ATRIAL FIBRILLATION ( 18 FDA reports)
CARDIOMEGALY ( 17 FDA reports)
CORONARY ARTERY DISEASE ( 16 FDA reports)
DIARRHOEA ( 16 FDA reports)
EMOTIONAL DISORDER ( 16 FDA reports)
PANCYTOPENIA ( 16 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 16 FDA reports)
ANGINA PECTORIS ( 15 FDA reports)
CONTUSION ( 15 FDA reports)
HAEMATURIA ( 15 FDA reports)
PAIN IN EXTREMITY ( 15 FDA reports)
PULMONARY HAEMORRHAGE ( 15 FDA reports)
RASH ( 15 FDA reports)
RHINORRHOEA ( 15 FDA reports)
SEPSIS ( 15 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 14 FDA reports)
BONE DISORDER ( 14 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 14 FDA reports)
DEHYDRATION ( 14 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 14 FDA reports)
NEUROPATHY PERIPHERAL ( 14 FDA reports)
OSTEONECROSIS ( 14 FDA reports)
PULMONARY OEDEMA ( 14 FDA reports)
ABDOMINAL PAIN ( 13 FDA reports)
ACTINOMYCOSIS ( 13 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 13 FDA reports)
AORTIC VALVE STENOSIS ( 13 FDA reports)
ATELECTASIS ( 13 FDA reports)
BLOOD BILIRUBIN INCREASED ( 13 FDA reports)
CHEST PAIN ( 13 FDA reports)
CHOLELITHIASIS ( 13 FDA reports)
DISEASE PROGRESSION ( 13 FDA reports)
EJECTION FRACTION DECREASED ( 13 FDA reports)
FEBRILE NEUTROPENIA ( 13 FDA reports)
HYDRONEPHROSIS ( 13 FDA reports)
HYPERCHOLESTEROLAEMIA ( 13 FDA reports)
HYPERLIPIDAEMIA ( 13 FDA reports)
INFLAMMATION ( 13 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 13 FDA reports)
OESOPHAGEAL ULCER ( 13 FDA reports)
OESOPHAGITIS ( 13 FDA reports)
ORAL DISCHARGE ( 13 FDA reports)
ORAL DISCOMFORT ( 13 FDA reports)
OSTEOMYELITIS ( 13 FDA reports)
PALPITATIONS ( 13 FDA reports)
PERIODONTAL DISEASE ( 13 FDA reports)
RENAL FAILURE CHRONIC ( 13 FDA reports)
VERTIGO ( 13 FDA reports)
WOUND ( 13 FDA reports)
ABDOMINAL PAIN UPPER ( 12 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 12 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 12 FDA reports)
ASPIRATION ( 12 FDA reports)
BONE LESION ( 12 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 12 FDA reports)
DECREASED APPETITE ( 12 FDA reports)
DEFORMITY ( 12 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 12 FDA reports)
DISCOMFORT ( 12 FDA reports)
EMPHYSEMA ( 12 FDA reports)
FALL ( 12 FDA reports)
GINGIVAL ULCERATION ( 12 FDA reports)
HEPATIC STEATOSIS ( 12 FDA reports)
HIP ARTHROPLASTY ( 12 FDA reports)
HYPOPHAGIA ( 12 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 12 FDA reports)
LIFE EXPECTANCY SHORTENED ( 12 FDA reports)
LOOSE TOOTH ( 12 FDA reports)
NEPHROLITHIASIS ( 12 FDA reports)
ORAL CAVITY FISTULA ( 12 FDA reports)
ORGAN FAILURE ( 12 FDA reports)
OSTEONECROSIS OF JAW ( 12 FDA reports)
OSTEOPENIA ( 12 FDA reports)
PAPILLOMA ( 12 FDA reports)
PERIODONTITIS ( 12 FDA reports)
PNEUMOCONIOSIS ( 12 FDA reports)
PRIMARY SEQUESTRUM ( 12 FDA reports)
PSYCHOLOGICAL TRAUMA ( 12 FDA reports)
RESPIRATORY FAILURE ( 12 FDA reports)
SURGERY ( 12 FDA reports)
TOOTH REPAIR ( 12 FDA reports)
TUMOUR INVASION ( 12 FDA reports)
VENTRICULAR HYPERTROPHY ( 12 FDA reports)
WRONG DRUG ADMINISTERED ( 12 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
BLOOD UREA INCREASED ( 11 FDA reports)
CARDIAC ARREST ( 11 FDA reports)
CARDIAC FAILURE ( 11 FDA reports)
CONFUSIONAL STATE ( 11 FDA reports)
DEEP VEIN THROMBOSIS ( 11 FDA reports)
DENTAL CARE ( 11 FDA reports)
GAMMOPATHY ( 11 FDA reports)
OSTEOARTHRITIS ( 11 FDA reports)
PROTHROMBIN TIME PROLONGED ( 11 FDA reports)
ASBESTOSIS ( 10 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 10 FDA reports)
BLOOD CALCIUM DECREASED ( 10 FDA reports)
CHROMATURIA ( 10 FDA reports)
COUGH ( 10 FDA reports)
GINGIVAL BLEEDING ( 10 FDA reports)
HAEMATOMA ( 10 FDA reports)
HAEMOGLOBIN DECREASED ( 10 FDA reports)
HAEMOPTYSIS ( 10 FDA reports)
LYMPHADENOPATHY ( 10 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 10 FDA reports)
MELAENA ( 10 FDA reports)
MULTIPLE MYELOMA ( 10 FDA reports)
PLEURAL FIBROSIS ( 10 FDA reports)
PSYCHIATRIC SYMPTOM ( 10 FDA reports)
RESPIRATORY DISTRESS ( 10 FDA reports)
THROMBOSIS ( 10 FDA reports)
TINEA PEDIS ( 10 FDA reports)
BILE DUCT STONE ( 9 FDA reports)
BLOOD CREATININE DECREASED ( 9 FDA reports)
BLOOD CREATININE INCREASED ( 9 FDA reports)
BLOOD POTASSIUM DECREASED ( 9 FDA reports)
GASTRITIS EROSIVE ( 9 FDA reports)
JAUNDICE CHOLESTATIC ( 9 FDA reports)
LUNG NEOPLASM ( 9 FDA reports)
PETECHIAE ( 9 FDA reports)
PROSTATOMEGALY ( 9 FDA reports)
PULMONARY FIBROSIS ( 9 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 9 FDA reports)
TREMOR ( 9 FDA reports)
URINARY TRACT INFECTION ( 9 FDA reports)
AORTIC VALVE REPLACEMENT ( 8 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 8 FDA reports)
BLOOD GLUCOSE INCREASED ( 8 FDA reports)
BODY TINEA ( 8 FDA reports)
BRADYCARDIA ( 8 FDA reports)
CALCULUS URETHRAL ( 8 FDA reports)
CELLULITIS ( 8 FDA reports)
CHEST X-RAY ABNORMAL ( 8 FDA reports)
CONDITION AGGRAVATED ( 8 FDA reports)
CONVULSION ( 8 FDA reports)
DEBRIDEMENT ( 8 FDA reports)
DEMENTIA ( 8 FDA reports)
DERMATITIS ATOPIC ( 8 FDA reports)
FACTOR VIII INHIBITION ( 8 FDA reports)
GINGIVITIS ( 8 FDA reports)
HEPATIC CIRRHOSIS ( 8 FDA reports)
HYPOXIA ( 8 FDA reports)
INTERTRIGO ( 8 FDA reports)
LEFT ATRIAL DILATATION ( 8 FDA reports)
LITHOTRIPSY ( 8 FDA reports)
LUNG DISORDER ( 8 FDA reports)
MENTAL STATUS CHANGES ( 8 FDA reports)
SCHAMBERG'S DISEASE ( 8 FDA reports)
SPINAL DISORDER ( 8 FDA reports)
STASIS DERMATITIS ( 8 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 8 FDA reports)
URETERAL STENT INSERTION ( 8 FDA reports)
VENTRICULAR TACHYCARDIA ( 8 FDA reports)
VIRAL INFECTION ( 8 FDA reports)
ACUTE RESPIRATORY FAILURE ( 7 FDA reports)
CLOSTRIDIAL INFECTION ( 7 FDA reports)
DECUBITUS ULCER ( 7 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 7 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 7 FDA reports)
JOINT EFFUSION ( 7 FDA reports)
NEUTROPENIA ( 7 FDA reports)
NIGHT SWEATS ( 7 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 7 FDA reports)
OSTEOPOROSIS ( 7 FDA reports)
PULMONARY EMBOLISM ( 7 FDA reports)
ROTATOR CUFF SYNDROME ( 7 FDA reports)
SWELLING FACE ( 7 FDA reports)
TENOSYNOVITIS STENOSANS ( 7 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 7 FDA reports)
ABDOMINAL DISTENSION ( 6 FDA reports)
BLOOD ALBUMIN DECREASED ( 6 FDA reports)
CAECITIS ( 6 FDA reports)
CHILLS ( 6 FDA reports)
COAGULOPATHY ( 6 FDA reports)
ESCHERICHIA INFECTION ( 6 FDA reports)
GANGRENE ( 6 FDA reports)
GASTROENTERITIS ( 6 FDA reports)
HAEMATEMESIS ( 6 FDA reports)
HEART RATE INCREASED ( 6 FDA reports)
HEMIPARESIS ( 6 FDA reports)
ILEUS PARALYTIC ( 6 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 6 FDA reports)
LETHARGY ( 6 FDA reports)
LUNG INFECTION ( 6 FDA reports)
NEPHROPATHY ( 6 FDA reports)
POST PROCEDURAL COMPLICATION ( 6 FDA reports)
RENAL TUBULAR NECROSIS ( 6 FDA reports)
SALIVARY GLAND CALCULUS ( 6 FDA reports)
AMNESIA ( 5 FDA reports)
ANAPHYLACTIC REACTION ( 5 FDA reports)
ASCITES ( 5 FDA reports)
BLOOD POTASSIUM INCREASED ( 5 FDA reports)
BONE MARROW RETICULIN FIBROSIS ( 5 FDA reports)
CARDIORENAL SYNDROME ( 5 FDA reports)
CEREBRAL HAEMORRHAGE ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 5 FDA reports)
ENCEPHALOPATHY ( 5 FDA reports)
ENTEROBACTER PNEUMONIA ( 5 FDA reports)
GLOBULINS INCREASED ( 5 FDA reports)
HAEMOLYTIC ANAEMIA ( 5 FDA reports)
HAEMORRHOIDS ( 5 FDA reports)
HEPATITIS C ( 5 FDA reports)
IMPAIRED HEALING ( 5 FDA reports)
INJECTION SITE INFECTION ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
INTERCEPTED MEDICATION ERROR ( 5 FDA reports)
METABOLIC ACIDOSIS ( 5 FDA reports)
METASTASES TO BONE ( 5 FDA reports)
MUSCLE HAEMORRHAGE ( 5 FDA reports)
MUSCLE INJURY ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
MYELOFIBROSIS ( 5 FDA reports)
ORTHOSTATIC HYPOTENSION ( 5 FDA reports)
OSTEOSCLEROSIS ( 5 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 5 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 5 FDA reports)
PROSTATIC INTRAEPITHELIAL NEOPLASIA ( 5 FDA reports)
PROTEIN TOTAL DECREASED ( 5 FDA reports)
PROTEIN TOTAL INCREASED ( 5 FDA reports)
PURPURA ( 5 FDA reports)
RENAL DISORDER ( 5 FDA reports)
SINUS TACHYCARDIA ( 5 FDA reports)
SKIN ULCER ( 5 FDA reports)
SPEECH DISORDER ( 5 FDA reports)
SPINAL COMPRESSION FRACTURE ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 5 FDA reports)
TACHYPNOEA ( 5 FDA reports)
TROPONIN INCREASED ( 5 FDA reports)
UNRESPONSIVE TO STIMULI ( 5 FDA reports)
VOMITING ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
ABASIA ( 4 FDA reports)
ALOPECIA ( 4 FDA reports)
ANGINA UNSTABLE ( 4 FDA reports)
APPENDICECTOMY ( 4 FDA reports)
AUTOIMMUNE HEPATITIS ( 4 FDA reports)
BACTERIA STOOL IDENTIFIED ( 4 FDA reports)
BLINDNESS ( 4 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
BLOOD SODIUM DECREASED ( 4 FDA reports)
CARDIAC ANEURYSM ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
CARDIOGENIC SHOCK ( 4 FDA reports)
CATHETER SITE HAEMORRHAGE ( 4 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 4 FDA reports)
DENTAL OPERATION ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
DIZZINESS POSTURAL ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
DYSURIA ( 4 FDA reports)
ECCHYMOSIS ( 4 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 4 FDA reports)
FLUID RETENTION ( 4 FDA reports)
GASTRIC ULCER ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
GROIN PAIN ( 4 FDA reports)
HAEMOLYSIS ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
HIATUS HERNIA ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
INCISIONAL HERNIA, OBSTRUCTIVE ( 4 FDA reports)
INCONTINENCE ( 4 FDA reports)
INFECTION ( 4 FDA reports)
INTRACRANIAL ANEURYSM ( 4 FDA reports)
KYPHOSIS ( 4 FDA reports)
LEUKAEMIA ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
LUNG INFILTRATION ( 4 FDA reports)
MALAISE ( 4 FDA reports)
MIGRAINE ( 4 FDA reports)
MORTON'S NEUROMA ( 4 FDA reports)
NEURALGIA ( 4 FDA reports)
PANCREATITIS ACUTE ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
PNEUMONIA KLEBSIELLA ( 4 FDA reports)
PULMONARY HYPERTENSION ( 4 FDA reports)
SYSTEMIC CANDIDA ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
AORTIC VALVE REPAIR ( 3 FDA reports)
APHASIA ( 3 FDA reports)
APLASIA PURE RED CELL ( 3 FDA reports)
BLAST CELL COUNT INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BLOOD LACTIC ACID INCREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
BLOOD URINE PRESENT ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
CARDIOVASCULAR DISORDER ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
DERMATITIS BULLOUS ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 3 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
FUNGUS CULTURE POSITIVE ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
GYNAECOMASTIA ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HEAD INJURY ( 3 FDA reports)
HEART VALVE INCOMPETENCE ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HOSPITALISATION ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
LEUKAEMIA RECURRENT ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
MOUTH HAEMORRHAGE ( 3 FDA reports)
MUSCLE TIGHTNESS ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
NEUROLOGICAL SYMPTOM ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 3 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 3 FDA reports)
OPERATIVE HAEMORRHAGE ( 3 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 3 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RESTLESS LEGS SYNDROME ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
SWELLING ( 3 FDA reports)
VAGINAL HAEMORRHAGE ( 3 FDA reports)
VASCULAR GRAFT OCCLUSION ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ABSCESS INTESTINAL ( 2 FDA reports)
ACUTE LEUKAEMIA ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ANAEMIA MACROCYTIC ( 2 FDA reports)
ANAL FISSURE ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
ANORECTAL CELLULITIS ( 2 FDA reports)
ANORECTAL VARICES HAEMORRHAGE ( 2 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ASPIRATION BONE MARROW ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BACTERIAL TEST POSITIVE ( 2 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 2 FDA reports)
BLAST CELLS PRESENT ( 2 FDA reports)
BLOOD BLISTER ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD MAGNESIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOODY DISCHARGE ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BONE MARROW TRANSPLANT ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CATHETER SITE HAEMATOMA ( 2 FDA reports)
CHRONIC SINUSITIS ( 2 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 2 FDA reports)
COAGULATION FACTOR VIII LEVEL DECREASED ( 2 FDA reports)
CULTURE STOOL POSITIVE ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
ENDOCARDITIS BACTERIAL ( 2 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
EXOSTOSIS ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FAILURE TO THRIVE ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FUNGAEMIA ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GLIOBLASTOMA MULTIFORME ( 2 FDA reports)
GRAFT THROMBOSIS ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HEPATORENAL SYNDROME ( 2 FDA reports)
HODGKIN'S DISEASE ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 2 FDA reports)
INAPPROPRIATE AFFECT ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFUSION SITE SWELLING ( 2 FDA reports)
INTRACARDIAC THROMBUS ( 2 FDA reports)
JAW DISORDER ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
MARROW HYPERPLASIA ( 2 FDA reports)
MASS ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MUSCLE STRAIN ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NERVE COMPRESSION ( 2 FDA reports)
NERVE INJURY ( 2 FDA reports)
NOCTURIA ( 2 FDA reports)
NUCLEATED RED CELLS ( 2 FDA reports)
OBESITY ( 2 FDA reports)
OCCULT BLOOD POSITIVE ( 2 FDA reports)
OCULAR ICTERUS ( 2 FDA reports)
ORAL HERPES ( 2 FDA reports)
ORAL MUCOSAL PETECHIAE ( 2 FDA reports)
OVARIAN CANCER METASTATIC ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PO2 INCREASED ( 2 FDA reports)
PORTAL HYPERTENSION ( 2 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PULMONARY MASS ( 2 FDA reports)
PURULENT DISCHARGE ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
REFRACTORY ANAEMIA ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
RETICULOCYTOSIS ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
SEPTIC PHLEBITIS ( 2 FDA reports)
SINUS CONGESTION ( 2 FDA reports)
SINUS HEADACHE ( 2 FDA reports)
SKIN NODULE ( 2 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
TACHYARRHYTHMIA ( 2 FDA reports)
TELANGIECTASIA ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
URETERIC OBSTRUCTION ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VARICES OESOPHAGEAL ( 2 FDA reports)
VENA CAVA FILTER INSERTION ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VIRAL RASH ( 2 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABSCESS ORAL ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADRENAL SUPPRESSION ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPENDICITIS PERFORATED ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
BASOPHILIA ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD IRON ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRONCHOGRAM ABNORMAL ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIAC PACEMAKER REVISION ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL HAEMORRHAGE TRAUMATIC ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 1 FDA reports)
COAGULATION TIME SHORTENED ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 1 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EVANS SYNDROME ( 1 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FAECALITH ( 1 FDA reports)
FEEDING TUBE COMPLICATION ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FRACTURED COCCYX ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GASTROINTESTINAL FISTULA ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
HAEMORRHAGE URINARY TRACT ( 1 FDA reports)
HAND AMPUTATION ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART RATE ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPARIN RESISTANCE ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEREDITARY ANGIOEDEMA ( 1 FDA reports)
HEREDITARY HAEMORRHAGIC TELANGIECTASIA ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOCHROMASIA ( 1 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INHIBITING ANTIBODIES ( 1 FDA reports)
INTERCEPTED DRUG ADMINISTRATION ERROR ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
ISOIMMUNISATION ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
MALIGNANT PALATE NEOPLASM ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 1 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
MYOCARDIAL HAEMORRHAGE ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NEUTROPHIL FUNCTION DISORDER ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIOSTITIS ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULSE PRESSURE INCREASED ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RESIDUAL URINE ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
RETCHING ( 1 FDA reports)
SALIVARY GLAND CANCER ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITAMIN B12 DECREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WOUND DECOMPOSITION ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)

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