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

RESPIRATORY FAILURE ( 36 FDA reports)
MULTI-ORGAN FAILURE ( 28 FDA reports)
RENAL FAILURE ( 28 FDA reports)
HYPOTENSION ( 27 FDA reports)
SEPTIC SHOCK ( 26 FDA reports)
HEPATIC FAILURE ( 23 FDA reports)
RENAL FAILURE ACUTE ( 21 FDA reports)
DEATH ( 18 FDA reports)
HYPERKALAEMIA ( 18 FDA reports)
HYPERBILIRUBINAEMIA ( 17 FDA reports)
CONVULSION ( 16 FDA reports)
BRADYCARDIA ( 14 FDA reports)
SEPSIS ( 14 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 14 FDA reports)
DRUG INEFFECTIVE ( 13 FDA reports)
INTESTINAL PERFORATION ( 12 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 12 FDA reports)
DEVICE RELATED INFECTION ( 10 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 10 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
THROMBOCYTOPENIA ( 9 FDA reports)
MUCOSAL INFLAMMATION ( 8 FDA reports)
ABSCESS ( 7 FDA reports)
DEHYDRATION ( 7 FDA reports)
DIVERTICULAR PERFORATION ( 7 FDA reports)
PULMONARY EMBOLISM ( 7 FDA reports)
ASTHENIA ( 6 FDA reports)
FEBRILE NEUTROPENIA ( 6 FDA reports)
FUNGAL INFECTION ( 6 FDA reports)
METABOLIC ACIDOSIS ( 6 FDA reports)
PNEUMONIA BACTERIAL ( 6 FDA reports)
STAPHYLOCOCCAL INFECTION ( 6 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
BLOOD CULTURE POSITIVE ( 5 FDA reports)
COAGULOPATHY ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
FLUID OVERLOAD ( 5 FDA reports)
FUNGAEMIA ( 5 FDA reports)
HYPOXIA ( 5 FDA reports)
LACTIC ACIDOSIS ( 5 FDA reports)
LIVER INJURY ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
PSEUDOMONAS INFECTION ( 5 FDA reports)
RESPIRATORY DISTRESS ( 5 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
ACUTE HEPATIC FAILURE ( 4 FDA reports)
ANTITHROMBIN III DECREASED ( 4 FDA reports)
BLOOD POTASSIUM INCREASED ( 4 FDA reports)
CATHETER RELATED INFECTION ( 4 FDA reports)
CELLULITIS GANGRENOUS ( 4 FDA reports)
COMMUNICATION DISORDER ( 4 FDA reports)
DIALYSIS ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
FIBRIN D DIMER INCREASED ( 4 FDA reports)
HYPOCOAGULABLE STATE ( 4 FDA reports)
ILEUS ( 4 FDA reports)
INFUSION RELATED REACTION ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
KLEBSIELLA BACTERAEMIA ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
PERIPHERAL ISCHAEMIA ( 4 FDA reports)
PULMONARY MYCOSIS ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
VAGINAL CELLULITIS ( 4 FDA reports)
VENTRICULAR FIBRILLATION ( 4 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
ANURIA ( 3 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 3 FDA reports)
CARDIOGENIC SHOCK ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 3 FDA reports)
EMPYEMA ( 3 FDA reports)
ESCHERICHIA TEST POSITIVE ( 3 FDA reports)
EXTREMITY NECROSIS ( 3 FDA reports)
GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
HAEMODYNAMIC INSTABILITY ( 3 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 3 FDA reports)
HEPATITIS TOXIC ( 3 FDA reports)
MEDIASTINITIS ( 3 FDA reports)
MULTI-ORGAN DISORDER ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
OESOPHAGEAL PERFORATION ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PATHOGEN RESISTANCE ( 3 FDA reports)
PERITONITIS BACTERIAL ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RECTAL OBSTRUCTION ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
SYSTEMIC CANDIDA ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ABDOMINAL SEPSIS ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CANDIDA PNEUMONIA ( 2 FDA reports)
CANDIDA TEST POSITIVE ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CRYING ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DUODENAL PERFORATION ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 2 FDA reports)
ENTEROCUTANEOUS FISTULA ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FUNGAL SEPSIS ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMATOMA INFECTION ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HERPES SIMPLEX ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIVER ABSCESS ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 2 FDA reports)
LOCALISED OEDEMA ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
MUCOSAL HAEMORRHAGE ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 2 FDA reports)
NEPHRITIC SYNDROME ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PARALYSIS FLACCID ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RASH ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN NODULE ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TROPONIN I INCREASED ( 2 FDA reports)
VAGINAL CANDIDIASIS ( 2 FDA reports)
VENOOCCLUSIVE DISEASE ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANISOCYTOSIS ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ASPERGILLUS TEST ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD LACTIC ACID ABNORMAL ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PYRUVIC ACID INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BRAIN HYPOXIA ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CATHETER CULTURE POSITIVE ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
COUGH ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENTEROBACTER TEST POSITIVE ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EUBACTERIUM INFECTION ( 1 FDA reports)
FALL ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FIBRIN D DIMER DECREASED ( 1 FDA reports)
FUNGAL PERITONITIS ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HERNIAL EVENTRATION ( 1 FDA reports)
HERPES OPHTHALMIC ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HERPES ZOSTER INFECTION NEUROLOGICAL ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HYDROPNEUMOTHORAX ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
ILEAL PERFORATION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIVER GRAFT LOSS ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SEVERE ACUTE RESPIRATORY SYNDROME ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
SYSTEMIC MYCOSIS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRICHOSPORON INFECTION ( 1 FDA reports)
UNRELATED DONOR BONE MARROW TRANSPLANTATION THERAPY ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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