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

ATRIAL FIBRILLATION ( 14 FDA reports)
DRUG INTERACTION ( 12 FDA reports)
DIARRHOEA ( 10 FDA reports)
DYSPNOEA ( 10 FDA reports)
CONDITION AGGRAVATED ( 9 FDA reports)
HYPOTENSION ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 8 FDA reports)
TORSADE DE POINTES ( 8 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
FALL ( 7 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
PLEURAL EFFUSION ( 7 FDA reports)
RENAL FAILURE ACUTE ( 7 FDA reports)
ABDOMINAL DISTENSION ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ASTHENIA ( 6 FDA reports)
BRADYCARDIA ( 6 FDA reports)
HAEMOGLOBIN DECREASED ( 6 FDA reports)
MULTI-ORGAN FAILURE ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
CARDIAC FAILURE ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ACUTE RESPIRATORY FAILURE ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 4 FDA reports)
DRY THROAT ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
ASCITES ( 3 FDA reports)
BK VIRUS INFECTION ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
CYSTITIS HAEMORRHAGIC ( 3 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
FAECALOMA ( 3 FDA reports)
HAEMODYNAMIC INSTABILITY ( 3 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 3 FDA reports)
HYPERBILIRUBINAEMIA ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RENAL PAIN ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
TACHYPNOEA ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
VENTRICULAR TACHYCARDIA ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
APNOEA ( 2 FDA reports)
APPENDICITIS PERFORATED ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ENTEROCOCCAL SEPSIS ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HYPERMAGNESAEMIA ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INJURY ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
METABOLIC DISORDER ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
PAIN ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
POST PROCEDURAL PNEUMONIA ( 2 FDA reports)
PROCTALGIA ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RASH ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VIRAEMIA ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
AMYLOIDOSIS ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APPENDICEAL ABSCESS ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ABNORMAL ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLUBBING ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 1 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYSTITIS VIRAL ( 1 FDA reports)
CYTOLOGY ABNORMAL ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
FUNGAL ENDOCARDITIS ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GOUT ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMATOMA INFECTION ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC HAEMATOMA ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INTELLIGENCE TEST ABNORMAL ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
JOINT ARTHROPLASTY ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIMB CRUSHING INJURY ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MECHANICAL VENTILATION COMPLICATION ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO SPINE ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PATELLA FRACTURE ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
ROTAVIRUS INFECTION ( 1 FDA reports)
SCAB ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SEROSITIS ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN FIBROSIS ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SPIDER NAEVUS ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STAPHYLOCOCCUS TEST NEGATIVE ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TENSION ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WOUND EVISCERATION ( 1 FDA reports)

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