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

FALL ( 14 FDA reports)
DRUG INTERACTION ( 12 FDA reports)
RENAL FAILURE ACUTE ( 12 FDA reports)
INTERSTITIAL LUNG DISEASE ( 8 FDA reports)
PYREXIA ( 8 FDA reports)
RENAL FAILURE ( 8 FDA reports)
PERICARDIAL EFFUSION ( 7 FDA reports)
RHABDOMYOLYSIS ( 7 FDA reports)
HYPONATRAEMIA ( 6 FDA reports)
PANCYTOPENIA ( 6 FDA reports)
VOMITING ( 6 FDA reports)
ANAEMIA ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
DERMATITIS EXFOLIATIVE ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
CORONARY ARTERY DISEASE ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
INTESTINAL ISCHAEMIA ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
SKIN NECROSIS ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
TOXIC SKIN ERUPTION ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
BLISTER ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
DEATH ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PROTEINURIA ( 3 FDA reports)
PURPURA ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ANKYLOSING SPONDYLITIS ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
COUGH ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
EPICONDYLITIS ( 2 FDA reports)
GALACTORRHOEA ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
PRURIGO ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SKIN HAEMORRHAGE ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
BACTERIAL PYELONEPHRITIS ( 1 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 1 FDA reports)
BIOPSY BRONCHUS NORMAL ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CORTICOTROPHIN ABNORMAL ( 1 FDA reports)
BLOOD CREATINE ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BODY FAT DISORDER ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRIEF PSYCHOTIC DISORDER WITH MARKED STRESSORS ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMO-HYPODERMITIS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTERCOSTAL RETRACTION ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MIXED LIVER INJURY ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUCOSA VESICLE ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
OXYGEN SUPPLEMENTATION ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARANEOPLASTIC PEMPHIGUS ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PULMONARY EOSINOPHILIA ( 1 FDA reports)
PURPURA NON-THROMBOCYTOPENIC ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
TENSION ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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