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

ANAEMIA ( 6 FDA reports)
DIARRHOEA ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
HAEMATURIA ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
HYPOTENSION ( 4 FDA reports)
MALAISE ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
ANGINA PECTORIS ( 3 FDA reports)
AORTIC STENOSIS ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CLOSTRIDIUM COLITIS ( 3 FDA reports)
CORONARY ARTERY STENOSIS ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DRUG RESISTANCE ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
FALL ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
HEPATOJUGULAR REFLUX ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
STENT OCCLUSION ( 3 FDA reports)
VENTRICULAR FIBRILLATION ( 3 FDA reports)
VENTRICULAR HYPOKINESIA ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ANURIA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA RECURRENT ( 2 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE III ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BRONCHITIS CHRONIC ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
DYSHIDROSIS ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HYPOCHROMIC ANAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
INTESTINAL FISTULA INFECTION ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OPTIC NEUROPATHY ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SUPERINFECTION ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANIMAL BITE ( 1 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DEVICE INTOLERANCE ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPOCOMPLEMENTAEMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MEGAKARYOCYTES ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEITIS ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PERITONEAL FLUID ANALYSIS ABNORMAL ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHLEBITIS SUPERFICIAL ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URETHRAL PAIN ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VARICOSE ULCERATION ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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