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

HYPOTENSION ( 16 FDA reports)
RENAL FAILURE ACUTE ( 13 FDA reports)
PLEURAL EFFUSION ( 10 FDA reports)
ACUTE RESPIRATORY FAILURE ( 9 FDA reports)
CONFUSIONAL STATE ( 9 FDA reports)
PULMONARY OEDEMA ( 9 FDA reports)
PNEUMONIA ( 8 FDA reports)
SEPSIS ( 8 FDA reports)
BONE MARROW FAILURE ( 7 FDA reports)
HYPOXIA ( 7 FDA reports)
LUNG INFECTION ( 7 FDA reports)
PLATELET COUNT DECREASED ( 7 FDA reports)
AGGRESSION ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
DELIRIUM ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
RESPIRATORY DISTRESS ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
TACHYCARDIA ( 6 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 5 FDA reports)
BACK PAIN ( 5 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
CHOLELITHIASIS ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
PARANOIA ( 5 FDA reports)
SEPTIC SHOCK ( 5 FDA reports)
SHOCK ( 5 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
CULTURE URINE POSITIVE ( 4 FDA reports)
DIALYSIS ( 4 FDA reports)
DYSURIA ( 4 FDA reports)
ESCHERICHIA BACTERAEMIA ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DIVERTICULAR PERFORATION ( 3 FDA reports)
DIVERTICULITIS ( 3 FDA reports)
ENTEROCOCCAL INFECTION ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HALLUCINATIONS, MIXED ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
ILEUS ( 3 FDA reports)
INFECTION ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
LUNG NEOPLASM ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
PERSECUTORY DELUSION ( 3 FDA reports)
RASH MACULO-PAPULAR ( 3 FDA reports)
SKIN WARM ( 3 FDA reports)
STEM CELL TRANSPLANT ( 3 FDA reports)
STRABISMUS ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABDOMINAL ADHESIONS ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANGIOSCLEROSIS ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ARTERIAL THROMBOSIS ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 2 FDA reports)
COLON CANCER STAGE IV ( 2 FDA reports)
COMA ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FALL ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HELICOBACTER INFECTION ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC HAEMORRHAGE ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
INTESTINAL DILATATION ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
INTESTINAL STOMA COMPLICATION ( 2 FDA reports)
LABORATORY TEST INTERFERENCE ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MELANOSIS COLI ( 2 FDA reports)
MENORRHAGIA ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 2 FDA reports)
OBESITY ( 2 FDA reports)
OVARIAN ENLARGEMENT ( 2 FDA reports)
PAIN ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 2 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PNEUMONIA FUNGAL ( 2 FDA reports)
PNEUMONIA VIRAL ( 2 FDA reports)
POSTOPERATIVE HERNIA ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RASH ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
SWELLING ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
URINARY TRACT OBSTRUCTION ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACCIDENT AT HOME ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
ANTICHOLINERGIC SYNDROME ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
APLASIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATABOLIC STATE ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CLEFT LIP AND PALATE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISSEMINATED CRYPTOCOCCOSIS ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENTEROBACTER BACTERAEMIA ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROINTESTINAL DISORDER POSTOPERATIVE ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
KERATITIS HERPETIC ( 1 FDA reports)
LACTOBACILLUS INFECTION ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MICROTIA ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONIA ESCHERICHIA ( 1 FDA reports)
PNEUMONIA PARAINFLUENZAE VIRAL ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL VESSEL DISORDER ( 1 FDA reports)
REPERFUSION INJURY ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SMALL INTESTINE ULCER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
VASCULAR INSUFFICIENCY ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)

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