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

ANAPHYLACTIC REACTION ( 8 FDA reports)
ANAEMIA ( 5 FDA reports)
SEPTIC SHOCK ( 5 FDA reports)
ANGIONEUROTIC OEDEMA ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
ASCITES ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CARDIOGENIC SHOCK ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
FALL ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
PANCREATIC NECROSIS ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 3 FDA reports)
SUPERINFECTION ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DEATH ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
TENOSYNOVITIS ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COUGH ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
FOREARM FRACTURE ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GUTTATE PSORIASIS ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPEROSMOLAR STATE ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEURITIS ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OVARIAN CANCER METASTATIC ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POIKILOCYTOSIS ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL HYPERTROPHY ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
VOMITING ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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