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

ASCITES INFECTION ( 6 FDA reports)
INCISIONAL HERNIA ( 6 FDA reports)
RENAL FAILURE ( 5 FDA reports)
BACK PAIN ( 4 FDA reports)
ENTEROCOCCAL INFECTION ( 4 FDA reports)
HEPATIC ARTERY STENOSIS ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
ANXIETY ( 3 FDA reports)
BILE DUCT STENOSIS ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
ENTEROBACTER INFECTION ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
POST PROCEDURAL BILE LEAK ( 3 FDA reports)
TREMOR ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
HAIR TEXTURE ABNORMAL ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
MALAISE ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
RASH ( 2 FDA reports)
TRANSFUSION REACTION ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANION GAP DECREASED ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BILIARY ANASTOMOSIS ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYST ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
FIBRINOUS BRONCHITIS ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC VEIN STENOSIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTURING ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETCHING ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCAB ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
VEILLONELLA INFECTION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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