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

HYPOKALAEMIA ( 295 FDA reports)
RENAL FAILURE ( 199 FDA reports)
RENAL IMPAIRMENT ( 195 FDA reports)
PYREXIA ( 192 FDA reports)
SEPSIS ( 183 FDA reports)
MULTI-ORGAN FAILURE ( 182 FDA reports)
RESPIRATORY FAILURE ( 169 FDA reports)
PNEUMONIA ( 167 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 154 FDA reports)
PLATELET COUNT DECREASED ( 154 FDA reports)
BLOOD BILIRUBIN INCREASED ( 139 FDA reports)
RENAL FAILURE ACUTE ( 136 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 135 FDA reports)
DRUG INEFFECTIVE ( 121 FDA reports)
ANAEMIA ( 117 FDA reports)
PANCYTOPENIA ( 117 FDA reports)
RHABDOMYOLYSIS ( 114 FDA reports)
DIARRHOEA ( 105 FDA reports)
BLOOD CREATININE INCREASED ( 103 FDA reports)
FEBRILE NEUTROPENIA ( 102 FDA reports)
PLEURAL EFFUSION ( 101 FDA reports)
HYPOTENSION ( 99 FDA reports)
THROMBOCYTOPENIA ( 96 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 92 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 90 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 90 FDA reports)
HAEMOGLOBIN DECREASED ( 89 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 85 FDA reports)
CONDITION AGGRAVATED ( 81 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 81 FDA reports)
DYSPNOEA ( 80 FDA reports)
SEPTIC SHOCK ( 80 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 77 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 76 FDA reports)
DEATH ( 75 FDA reports)
NAUSEA ( 74 FDA reports)
DRUG INTERACTION ( 73 FDA reports)
INFECTION ( 73 FDA reports)
BLOOD UREA INCREASED ( 72 FDA reports)
NEUTROPENIA ( 71 FDA reports)
VOMITING ( 70 FDA reports)
CARDIAC ARREST ( 68 FDA reports)
FUNGAL INFECTION ( 68 FDA reports)
BLOOD POTASSIUM DECREASED ( 67 FDA reports)
CARDIO-RESPIRATORY ARREST ( 66 FDA reports)
LIVER DISORDER ( 65 FDA reports)
CHOLESTASIS ( 64 FDA reports)
HYPERKALAEMIA ( 63 FDA reports)
HYPERBILIRUBINAEMIA ( 60 FDA reports)
ABDOMINAL PAIN ( 58 FDA reports)
CARDIAC FAILURE ( 58 FDA reports)
RASH ( 58 FDA reports)
RENAL DISORDER ( 57 FDA reports)
CONVULSION ( 56 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 54 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 52 FDA reports)
ASTHENIA ( 51 FDA reports)
TACHYCARDIA ( 51 FDA reports)
ASPERGILLOSIS ( 49 FDA reports)
SHOCK ( 45 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 44 FDA reports)
CHILLS ( 42 FDA reports)
DISEASE PROGRESSION ( 42 FDA reports)
METABOLIC ACIDOSIS ( 42 FDA reports)
GRAFT VERSUS HOST DISEASE ( 40 FDA reports)
STAPHYLOCOCCAL INFECTION ( 40 FDA reports)
BLOOD PRESSURE DECREASED ( 39 FDA reports)
NEUTROPHIL COUNT DECREASED ( 39 FDA reports)
ASCITES ( 38 FDA reports)
ERYTHEMA ( 38 FDA reports)
INTERSTITIAL LUNG DISEASE ( 38 FDA reports)
PANCREATITIS ACUTE ( 38 FDA reports)
STEM CELL TRANSPLANT ( 38 FDA reports)
HAEMATOCRIT DECREASED ( 37 FDA reports)
HEADACHE ( 37 FDA reports)
PNEUMONIA FUNGAL ( 37 FDA reports)
HAEMODIALYSIS ( 36 FDA reports)
NEPHROPATHY TOXIC ( 36 FDA reports)
PULMONARY HAEMORRHAGE ( 36 FDA reports)
BONE MARROW FAILURE ( 35 FDA reports)
HEPATIC FAILURE ( 35 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 34 FDA reports)
HYPERTENSION ( 34 FDA reports)
INFUSION RELATED REACTION ( 33 FDA reports)
MUSCULAR WEAKNESS ( 33 FDA reports)
PULMONARY OEDEMA ( 33 FDA reports)
HYPOMAGNESAEMIA ( 32 FDA reports)
MALAISE ( 32 FDA reports)
MUCOSAL INFLAMMATION ( 32 FDA reports)
PRURITUS ( 32 FDA reports)
CONFUSIONAL STATE ( 31 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 31 FDA reports)
FATIGUE ( 31 FDA reports)
HYPERGLYCAEMIA ( 31 FDA reports)
HYPONATRAEMIA ( 31 FDA reports)
JAUNDICE ( 31 FDA reports)
LEUKOPENIA ( 31 FDA reports)
PANCREATITIS ( 31 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 30 FDA reports)
CYTOLYTIC HEPATITIS ( 30 FDA reports)
HYPERSENSITIVITY ( 30 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 30 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 30 FDA reports)
DIALYSIS ( 29 FDA reports)
LUNG INFILTRATION ( 29 FDA reports)
RENAL TUBULAR DISORDER ( 29 FDA reports)
VENTRICULAR FIBRILLATION ( 29 FDA reports)
BACK PAIN ( 28 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 28 FDA reports)
OXYGEN SATURATION DECREASED ( 28 FDA reports)
HAEMOPTYSIS ( 27 FDA reports)
TORSADE DE POINTES ( 27 FDA reports)
URINE OUTPUT DECREASED ( 27 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 26 FDA reports)
HYPOALBUMINAEMIA ( 26 FDA reports)
OEDEMA ( 26 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 26 FDA reports)
ZYGOMYCOSIS ( 26 FDA reports)
LUNG DISORDER ( 25 FDA reports)
OEDEMA PERIPHERAL ( 25 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 25 FDA reports)
RESPIRATORY DISTRESS ( 25 FDA reports)
WEIGHT INCREASED ( 25 FDA reports)
HAEMOLYSIS ( 24 FDA reports)
LOSS OF CONSCIOUSNESS ( 24 FDA reports)
NO THERAPEUTIC RESPONSE ( 24 FDA reports)
PERICARDITIS ( 24 FDA reports)
PSEUDOMONAS INFECTION ( 24 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 24 FDA reports)
RENAL TUBULAR ACIDOSIS ( 24 FDA reports)
RESPIRATORY DISORDER ( 24 FDA reports)
CAPILLARY LEAK SYNDROME ( 23 FDA reports)
CHEST PAIN ( 23 FDA reports)
ENCEPHALOPATHY ( 23 FDA reports)
POLYNEUROPATHY ( 23 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 23 FDA reports)
ACUTE HEPATIC FAILURE ( 22 FDA reports)
DRUG TOXICITY ( 22 FDA reports)
HYPERNATRAEMIA ( 22 FDA reports)
HYPOCALCAEMIA ( 22 FDA reports)
HYPOXIA ( 22 FDA reports)
PROTHROMBIN TIME PROLONGED ( 22 FDA reports)
BLOOD POTASSIUM INCREASED ( 21 FDA reports)
CIRCULATORY COLLAPSE ( 21 FDA reports)
DISTURBANCE IN ATTENTION ( 21 FDA reports)
HEPATITIS CHOLESTATIC ( 21 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 21 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 20 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 20 FDA reports)
COAGULOPATHY ( 20 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 20 FDA reports)
HAEMORRHAGE ( 20 FDA reports)
PLATELET COUNT INCREASED ( 20 FDA reports)
SOMNOLENCE ( 20 FDA reports)
BACTERAEMIA ( 19 FDA reports)
BLOOD ALBUMIN DECREASED ( 19 FDA reports)
BLOOD SODIUM DECREASED ( 19 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 19 FDA reports)
MEDICATION ERROR ( 19 FDA reports)
MYALGIA ( 19 FDA reports)
NEOPLASM PROGRESSION ( 19 FDA reports)
PAIN ( 19 FDA reports)
PERICARDIAL EFFUSION ( 19 FDA reports)
SHOCK HAEMORRHAGIC ( 19 FDA reports)
SINUSITIS ( 19 FDA reports)
VIRAL INFECTION ( 19 FDA reports)
ARRHYTHMIA ( 18 FDA reports)
ATRIAL FIBRILLATION ( 18 FDA reports)
CHEST X-RAY ABNORMAL ( 18 FDA reports)
DEHYDRATION ( 18 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 18 FDA reports)
DYSPHAGIA ( 18 FDA reports)
FLUSHING ( 18 FDA reports)
FUNGAL SEPSIS ( 18 FDA reports)
HAEMATURIA ( 18 FDA reports)
HEPATOMEGALY ( 18 FDA reports)
METABOLIC DISORDER ( 18 FDA reports)
MUCORMYCOSIS ( 18 FDA reports)
NEUROPATHY PERIPHERAL ( 18 FDA reports)
SYSTEMIC CANDIDA ( 18 FDA reports)
VENTRICULAR TACHYCARDIA ( 18 FDA reports)
ABDOMINAL DISTENSION ( 17 FDA reports)
ANTITHROMBIN III DECREASED ( 17 FDA reports)
ANURIA ( 17 FDA reports)
BRADYCARDIA ( 17 FDA reports)
CAECITIS ( 17 FDA reports)
CANDIDIASIS ( 17 FDA reports)
DRUG ERUPTION ( 17 FDA reports)
FUNGAEMIA ( 17 FDA reports)
HEPATOTOXICITY ( 17 FDA reports)
HYPOVOLAEMIC SHOCK ( 17 FDA reports)
LUNG NEOPLASM ( 17 FDA reports)
NEOPLASM MALIGNANT ( 17 FDA reports)
PNEUMONIA BACTERIAL ( 17 FDA reports)
PURPURA ( 17 FDA reports)
TACHYPNOEA ( 17 FDA reports)
ABDOMINAL PAIN UPPER ( 16 FDA reports)
ACIDOSIS ( 16 FDA reports)
APLASIA ( 16 FDA reports)
B-CELL LYMPHOMA STAGE III ( 16 FDA reports)
BRAIN STEM HAEMORRHAGE ( 16 FDA reports)
COLON POLYPECTOMY ( 16 FDA reports)
GENERALISED OEDEMA ( 16 FDA reports)
HAPTOGLOBIN DECREASED ( 16 FDA reports)
LUNG INJURY ( 16 FDA reports)
MYOCARDITIS ( 16 FDA reports)
OSTEOARTHRITIS ( 16 FDA reports)
OSTEOPOROSIS ( 16 FDA reports)
PULMONARY MYCOSIS ( 16 FDA reports)
T-CELL LYMPHOMA STAGE III ( 16 FDA reports)
VARICOSE VEIN ( 16 FDA reports)
VENOUS STENT INSERTION ( 16 FDA reports)
ANAPHYLACTIC REACTION ( 15 FDA reports)
BLOOD CULTURE POSITIVE ( 15 FDA reports)
BRAIN HERNIATION ( 15 FDA reports)
CEREBRAL HAEMORRHAGE ( 15 FDA reports)
CLOSTRIDIAL INFECTION ( 15 FDA reports)
DISEASE RECURRENCE ( 15 FDA reports)
ENTEROCOCCAL INFECTION ( 15 FDA reports)
GAIT DISTURBANCE ( 15 FDA reports)
NERVOUS SYSTEM DISORDER ( 15 FDA reports)
OFF LABEL USE ( 15 FDA reports)
RESPIRATORY ARREST ( 15 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 14 FDA reports)
ANAPHYLACTIC SHOCK ( 14 FDA reports)
ANOREXIA ( 14 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 14 FDA reports)
BLOOD GLUCOSE INCREASED ( 14 FDA reports)
BLOOD URINE PRESENT ( 14 FDA reports)
CHEST DISCOMFORT ( 14 FDA reports)
CONSTIPATION ( 14 FDA reports)
DRUG RESISTANCE ( 14 FDA reports)
HEPATOCELLULAR DAMAGE ( 14 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 14 FDA reports)
HYPOACUSIS ( 14 FDA reports)
HYPOGLYCAEMIA ( 14 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 14 FDA reports)
OVERDOSE ( 14 FDA reports)
PULMONARY EMBOLISM ( 14 FDA reports)
TRANSAMINASES INCREASED ( 14 FDA reports)
TREMOR ( 14 FDA reports)
ACUTE PULMONARY OEDEMA ( 13 FDA reports)
ATELECTASIS ( 13 FDA reports)
COMA ( 13 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 13 FDA reports)
DECREASED APPETITE ( 13 FDA reports)
DISORIENTATION ( 13 FDA reports)
EJECTION FRACTION DECREASED ( 13 FDA reports)
ELECTROLYTE IMBALANCE ( 13 FDA reports)
HEART RATE INCREASED ( 13 FDA reports)
HYPERCAPNIA ( 13 FDA reports)
MYOCARDIAL INFARCTION ( 13 FDA reports)
NEUTROPENIC SEPSIS ( 13 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 13 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 13 FDA reports)
COUGH ( 12 FDA reports)
DEAFNESS ( 12 FDA reports)
DEVICE RELATED INFECTION ( 12 FDA reports)
FLUID RETENTION ( 12 FDA reports)
HYPERHIDROSIS ( 12 FDA reports)
ILEUS PARALYTIC ( 12 FDA reports)
LUNG INFECTION ( 12 FDA reports)
MENTAL STATUS CHANGES ( 12 FDA reports)
MUSCULOSKELETAL PAIN ( 12 FDA reports)
MYOCLONIC EPILEPSY ( 12 FDA reports)
MYOSITIS ( 12 FDA reports)
PNEUMONITIS ( 12 FDA reports)
SYSTEMIC MYCOSIS ( 12 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 12 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 11 FDA reports)
AGRANULOCYTOSIS ( 11 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 11 FDA reports)
ARTHRALGIA ( 11 FDA reports)
BACTERIAL INFECTION ( 11 FDA reports)
BACTERIAL SEPSIS ( 11 FDA reports)
CARDIOMYOPATHY ( 11 FDA reports)
CELLULITIS ( 11 FDA reports)
CEREBRAL FUNGAL INFECTION ( 11 FDA reports)
DIABETES MELLITUS ( 11 FDA reports)
ENDOCARDITIS ( 11 FDA reports)
HICCUPS ( 11 FDA reports)
INFLAMMATION ( 11 FDA reports)
MITRAL VALVE INCOMPETENCE ( 11 FDA reports)
MULTI-ORGAN DISORDER ( 11 FDA reports)
MYELODYSPLASTIC SYNDROME ( 11 FDA reports)
OLIGURIA ( 11 FDA reports)
RECTAL HAEMORRHAGE ( 11 FDA reports)
STEVENS-JOHNSON SYNDROME ( 11 FDA reports)
TUMOUR LYSIS SYNDROME ( 11 FDA reports)
ACUTE RESPIRATORY FAILURE ( 10 FDA reports)
AGITATION ( 10 FDA reports)
ANGIOEDEMA ( 10 FDA reports)
ATRIAL FLUTTER ( 10 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 10 FDA reports)
BLOOD PRESSURE INCREASED ( 10 FDA reports)
BONE MARROW TRANSPLANT ( 10 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 10 FDA reports)
CARDIAC TAMPONADE ( 10 FDA reports)
CEREBROVASCULAR ACCIDENT ( 10 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 10 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 10 FDA reports)
ESCHERICHIA INFECTION ( 10 FDA reports)
FUSARIUM INFECTION ( 10 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 10 FDA reports)
HEPATIC ENZYME INCREASED ( 10 FDA reports)
HYPERAMMONAEMIA ( 10 FDA reports)
MALNUTRITION ( 10 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 10 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 10 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 10 FDA reports)
RASH ERYTHEMATOUS ( 10 FDA reports)
RENAL TUBULAR NECROSIS ( 10 FDA reports)
SERUM FERRITIN INCREASED ( 10 FDA reports)
SPLENOMEGALY ( 10 FDA reports)
STOMATITIS ( 10 FDA reports)
TINNITUS ( 10 FDA reports)
TRANSFUSION ( 10 FDA reports)
UNRESPONSIVE TO STIMULI ( 10 FDA reports)
URINARY TRACT INFECTION ( 10 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 9 FDA reports)
ANTITHROMBIN III DEFICIENCY ( 9 FDA reports)
CEREBRAL INFARCTION ( 9 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 9 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 9 FDA reports)
DEEP VEIN THROMBOSIS ( 9 FDA reports)
DIPLOPIA ( 9 FDA reports)
EXOPHTHALMOS ( 9 FDA reports)
EXTRASYSTOLES ( 9 FDA reports)
HEPATIC ENCEPHALOPATHY ( 9 FDA reports)
HEPATOSPLENOMEGALY ( 9 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 9 FDA reports)
HYPERMAGNESAEMIA ( 9 FDA reports)
HYPOPHOSPHATAEMIA ( 9 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 9 FDA reports)
NEUROBLASTOMA RECURRENT ( 9 FDA reports)
NEUTROPENIC COLITIS ( 9 FDA reports)
NOCARDIOSIS ( 9 FDA reports)
PAIN IN EXTREMITY ( 9 FDA reports)
PATHOGEN RESISTANCE ( 9 FDA reports)
PETECHIAE ( 9 FDA reports)
PHOSPHENES ( 9 FDA reports)
POST PROCEDURAL COMPLICATION ( 9 FDA reports)
PROTEIN TOTAL DECREASED ( 9 FDA reports)
RASH GENERALISED ( 9 FDA reports)
SKIN LESION ( 9 FDA reports)
TREATMENT FAILURE ( 9 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 9 FDA reports)
ABDOMINAL DISCOMFORT ( 8 FDA reports)
ACCIDENTAL OVERDOSE ( 8 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 8 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 8 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 8 FDA reports)
BLOOD AMYLASE INCREASED ( 8 FDA reports)
BLOOD MAGNESIUM DECREASED ( 8 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 8 FDA reports)
BRONCHOSPASM ( 8 FDA reports)
CARDIAC FAILURE ACUTE ( 8 FDA reports)
COLITIS ( 8 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 8 FDA reports)
DERMATITIS EXFOLIATIVE ( 8 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 8 FDA reports)
DIZZINESS ( 8 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 8 FDA reports)
DYSKINESIA ( 8 FDA reports)
ENCEPHALITIS ( 8 FDA reports)
ENDOCARDITIS CANDIDA ( 8 FDA reports)
ENDOMETRIOSIS ( 8 FDA reports)
ENTEROCOCCAL SEPSIS ( 8 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 8 FDA reports)
FACIAL PALSY ( 8 FDA reports)
FLUID OVERLOAD ( 8 FDA reports)
GASTROINTESTINAL DISORDER ( 8 FDA reports)
HEART RATE DECREASED ( 8 FDA reports)
HEPATIC MASS ( 8 FDA reports)
HEPATITIS ACUTE ( 8 FDA reports)
HEPATITIS TOXIC ( 8 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 8 FDA reports)
LACTIC ACIDOSIS ( 8 FDA reports)
LAPAROSCOPIC STERILISATION ( 8 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 8 FDA reports)
MENINGITIS ( 8 FDA reports)
MOUTH HAEMORRHAGE ( 8 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 8 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 8 FDA reports)
PALPITATIONS ( 8 FDA reports)
PARAESTHESIA ( 8 FDA reports)
PROTEINURIA ( 8 FDA reports)
RESPIRATORY DEPRESSION ( 8 FDA reports)
SALPINGO-OOPHORECTOMY ( 8 FDA reports)
SPLENIC INFARCTION ( 8 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 8 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 8 FDA reports)
THYROIDECTOMY ( 8 FDA reports)
ANXIETY ( 7 FDA reports)
ASPIRATION ( 7 FDA reports)
BONE MARROW TOXICITY ( 7 FDA reports)
BRONCHITIS ( 7 FDA reports)
BRONCHOPNEUMONIA ( 7 FDA reports)
CARDIAC DISORDER ( 7 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 7 FDA reports)
CEREBRAL ASPERGILLOSIS ( 7 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 7 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 7 FDA reports)
CRYPTOCOCCOSIS ( 7 FDA reports)
CSF PROTEIN INCREASED ( 7 FDA reports)
DEAFNESS NEUROSENSORY ( 7 FDA reports)
EPISTAXIS ( 7 FDA reports)
FALL ( 7 FDA reports)
FLUID INTAKE REDUCED ( 7 FDA reports)
FUNGAL ENDOCARDITIS ( 7 FDA reports)
HAEMOLYTIC ANAEMIA ( 7 FDA reports)
HERPES SIMPLEX ( 7 FDA reports)
HYPERCALCAEMIA ( 7 FDA reports)
HYPOTHERMIA ( 7 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 7 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 7 FDA reports)
LETHARGY ( 7 FDA reports)
LEUKAEMIA ( 7 FDA reports)
LEUKOENCEPHALOPATHY ( 7 FDA reports)
MELAENA ( 7 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 7 FDA reports)
MUSCLE RIGIDITY ( 7 FDA reports)
MYDRIASIS ( 7 FDA reports)
PALLOR ( 7 FDA reports)
PNEUMONIA ASPIRATION ( 7 FDA reports)
PSEUDOMONAL SEPSIS ( 7 FDA reports)
RESTLESSNESS ( 7 FDA reports)
SINUSITIS FUNGAL ( 7 FDA reports)
THIRST ( 7 FDA reports)
TOXIC SKIN ERUPTION ( 7 FDA reports)
ABNORMAL BEHAVIOUR ( 6 FDA reports)
ALOPECIA ( 6 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 6 FDA reports)
BLINDNESS ( 6 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 6 FDA reports)
BLOOD URIC ACID INCREASED ( 6 FDA reports)
BODY TEMPERATURE INCREASED ( 6 FDA reports)
CANDIDA SEPSIS ( 6 FDA reports)
CARDIOPULMONARY FAILURE ( 6 FDA reports)
CONJUNCTIVAL OEDEMA ( 6 FDA reports)
CYANOSIS ( 6 FDA reports)
DELIRIUM ( 6 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 6 FDA reports)
ENTEROCOLITIS ( 6 FDA reports)
EYE MOVEMENT DISORDER ( 6 FDA reports)
EYE PAIN ( 6 FDA reports)
GASTRITIS ( 6 FDA reports)
HALLUCINATION ( 6 FDA reports)
HYPERPHOSPHATAEMIA ( 6 FDA reports)
ILEUS ( 6 FDA reports)
IMMUNOSUPPRESSION ( 6 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 6 FDA reports)
LYMPHOMA ( 6 FDA reports)
MUSCLE SPASMS ( 6 FDA reports)
MYOCLONUS ( 6 FDA reports)
MYOPATHY ( 6 FDA reports)
NEUROLOGICAL SYMPTOM ( 6 FDA reports)
NO ADVERSE EVENT ( 6 FDA reports)
OPHTHALMOPLEGIA ( 6 FDA reports)
PNEUMOTHORAX ( 6 FDA reports)
PULMONARY HYPERTENSION ( 6 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 6 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 6 FDA reports)
STENOTROPHOMONAS INFECTION ( 6 FDA reports)
STREPTOCOCCAL INFECTION ( 6 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 6 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 6 FDA reports)
WRONG DRUG ADMINISTERED ( 6 FDA reports)
ADENOVIRUS INFECTION ( 5 FDA reports)
ALVEOLAR PROTEINOSIS ( 5 FDA reports)
ANAPHYLACTOID REACTION ( 5 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 5 FDA reports)
BLOOD BICARBONATE DECREASED ( 5 FDA reports)
BLOOD CHLORIDE DECREASED ( 5 FDA reports)
BLOOD CREATINE INCREASED ( 5 FDA reports)
BLOOD CREATININE DECREASED ( 5 FDA reports)
BLOOD URIC ACID DECREASED ( 5 FDA reports)
BODY TEMPERATURE DECREASED ( 5 FDA reports)
BONE PAIN ( 5 FDA reports)
BRAIN ABSCESS ( 5 FDA reports)
BRAIN OEDEMA ( 5 FDA reports)
CARDIAC VALVE VEGETATION ( 5 FDA reports)
CARDIOGENIC SHOCK ( 5 FDA reports)
CELL DEATH ( 5 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 5 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 5 FDA reports)
COLD SWEAT ( 5 FDA reports)
CULTURE STOOL POSITIVE ( 5 FDA reports)
CULTURE URINE POSITIVE ( 5 FDA reports)
DIABETES INSIPIDUS ( 5 FDA reports)
DILATATION VENTRICULAR ( 5 FDA reports)
DRUG LEVEL INCREASED ( 5 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 5 FDA reports)
ERYTHEMA MULTIFORME ( 5 FDA reports)
EYE DISORDER ( 5 FDA reports)
FEBRILE BONE MARROW APLASIA ( 5 FDA reports)
GLOMERULONEPHRITIS ( 5 FDA reports)
GRAFT DYSFUNCTION ( 5 FDA reports)
HAEMATEMESIS ( 5 FDA reports)
HAEMODYNAMIC INSTABILITY ( 5 FDA reports)
HEPATIC INFARCTION ( 5 FDA reports)
HEPATORENAL FAILURE ( 5 FDA reports)
HYPERTHERMIA ( 5 FDA reports)
IMMUNE SYSTEM DISORDER ( 5 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 5 FDA reports)
ISCHAEMIA ( 5 FDA reports)
LIPIDS INCREASED ( 5 FDA reports)
MASS ( 5 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 5 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 5 FDA reports)
NEPHRITIS INTERSTITIAL ( 5 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 5 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 5 FDA reports)
ORAL HERPES ( 5 FDA reports)
PERICARDIAL HAEMORRHAGE ( 5 FDA reports)
PREMATURE DELIVERY ( 5 FDA reports)
PROTEIN URINE PRESENT ( 5 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 5 FDA reports)
RASH MACULO-PAPULAR ( 5 FDA reports)
RENAL INFARCT ( 5 FDA reports)
RESPIRATION ABNORMAL ( 5 FDA reports)
RESPIRATORY RATE INCREASED ( 5 FDA reports)
SKIN REACTION ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
TREATMENT NONCOMPLIANCE ( 5 FDA reports)
TRICHOSPORON INFECTION ( 5 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 5 FDA reports)
VASCULITIS ( 5 FDA reports)
VENOUS THROMBOSIS LIMB ( 5 FDA reports)
VENTRICULAR HYPERTROPHY ( 5 FDA reports)
VISUAL ACUITY REDUCED ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
WHEEZING ( 5 FDA reports)
ABDOMINAL TENDERNESS ( 4 FDA reports)
APALLIC SYNDROME ( 4 FDA reports)
APLASTIC ANAEMIA ( 4 FDA reports)
ASPERGILLUS TEST POSITIVE ( 4 FDA reports)
ASPHYXIA ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 4 FDA reports)
BILIARY TRACT DISORDER ( 4 FDA reports)
BLOOD GLUCOSE DECREASED ( 4 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 4 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 4 FDA reports)
BURNING SENSATION ( 4 FDA reports)
CARDIOTOXICITY ( 4 FDA reports)
CATHETER RELATED INFECTION ( 4 FDA reports)
CATHETER SITE INFECTION ( 4 FDA reports)
CEREBELLAR HAEMORRHAGE ( 4 FDA reports)
CHEMOTHERAPY ( 4 FDA reports)
CHOLECYSTITIS ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
CONJUNCTIVITIS ( 4 FDA reports)
COR PULMONALE ( 4 FDA reports)
CORYNEBACTERIUM INFECTION ( 4 FDA reports)
DELAYED ENGRAFTMENT ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 4 FDA reports)
DISCOMFORT ( 4 FDA reports)
DISEASE COMPLICATION ( 4 FDA reports)
DYSPHONIA ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 4 FDA reports)
ENGRAFTMENT SYNDROME ( 4 FDA reports)
EYELID PTOSIS ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
FEMUR FRACTURE ( 4 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 4 FDA reports)
FUNGAL SKIN INFECTION ( 4 FDA reports)
GASTROINTESTINAL NECROSIS ( 4 FDA reports)
GENERALISED ERYTHEMA ( 4 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 4 FDA reports)
GLYCOSURIA ( 4 FDA reports)
HAEMORRHAGIC DIATHESIS ( 4 FDA reports)
HAEMOSTASIS ( 4 FDA reports)
HEARING IMPAIRED ( 4 FDA reports)
HEPATITIS ( 4 FDA reports)
HEPATOCELLULAR INJURY ( 4 FDA reports)
HERPES VIRUS INFECTION ( 4 FDA reports)
HYDROCEPHALUS ( 4 FDA reports)
HYPERPYREXIA ( 4 FDA reports)
HYPERTONIA ( 4 FDA reports)
HYPERTRANSAMINASAEMIA ( 4 FDA reports)
HYPERURICAEMIA ( 4 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 4 FDA reports)
HYPOPROTEINAEMIA ( 4 FDA reports)
HYPOVOLAEMIA ( 4 FDA reports)
IGA NEPHROPATHY ( 4 FDA reports)
ILL-DEFINED DISORDER ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
INTESTINAL OBSTRUCTION ( 4 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 4 FDA reports)
LACTASE DEFICIENCY ( 4 FDA reports)
LEUKAEMIA RECURRENT ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
LUNG ABSCESS ( 4 FDA reports)
LUNG CONSOLIDATION ( 4 FDA reports)
LUNG NEOPLASM MALIGNANT ( 4 FDA reports)
MALLORY-WEISS SYNDROME ( 4 FDA reports)
METAMYELOCYTE PERCENTAGE INCREASED ( 4 FDA reports)
MYELOCYTE COUNT INCREASED ( 4 FDA reports)
MYELOCYTE PRESENT ( 4 FDA reports)
MYOPATHY TOXIC ( 4 FDA reports)
NECROSIS ( 4 FDA reports)
NEUROCRYPTOCOCCOSIS ( 4 FDA reports)
NEUROGENIC BLADDER ( 4 FDA reports)
NEUROTOXICITY ( 4 FDA reports)
NODULE ( 4 FDA reports)
OCCULT BLOOD POSITIVE ( 4 FDA reports)
ORAL PAIN ( 4 FDA reports)
ORTHOSTATIC HYPOTENSION ( 4 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 4 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 4 FDA reports)
PERSONALITY CHANGE ( 4 FDA reports)
PLEURITIC PAIN ( 4 FDA reports)
PNEUMONIA NECROTISING ( 4 FDA reports)
PULMONARY CONGESTION ( 4 FDA reports)
PULMONARY FIBROSIS ( 4 FDA reports)
PULMONARY MASS ( 4 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 4 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 4 FDA reports)
RENAL GRAFT LOSS ( 4 FDA reports)
RENAL HAEMORRHAGE ( 4 FDA reports)
RHINORRHOEA ( 4 FDA reports)
RIGHT VENTRICULAR FAILURE ( 4 FDA reports)
SCEDOSPORIUM INFECTION ( 4 FDA reports)
SEPTIC EMBOLUS ( 4 FDA reports)
SERRATIA INFECTION ( 4 FDA reports)
SKIN DISCOLOURATION ( 4 FDA reports)
SKIN NECROSIS ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
SUFFOCATION FEELING ( 4 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 4 FDA reports)
THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
THROMBOPHLEBITIS ( 4 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 4 FDA reports)
URINE OUTPUT INCREASED ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
VANISHING BILE DUCT SYNDROME ( 4 FDA reports)
VASCULAR PSEUDOANEURYSM ( 4 FDA reports)
VENOOCCLUSIVE DISEASE ( 4 FDA reports)
VENOUS THROMBOSIS ( 4 FDA reports)
VENTRICULAR DYSFUNCTION ( 4 FDA reports)
ABNORMAL SENSATION IN EYE ( 3 FDA reports)
ABSCESS ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 3 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 3 FDA reports)
ALVEOLITIS ( 3 FDA reports)
AMMONIA INCREASED ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA ( 3 FDA reports)
AORTIC RUPTURE ( 3 FDA reports)
AORTIC VALVE INCOMPETENCE ( 3 FDA reports)
APLASIA PURE RED CELL ( 3 FDA reports)
AREFLEXIA ( 3 FDA reports)
BLINDNESS UNILATERAL ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 3 FDA reports)
BLOOD LACTIC ACID INCREASED ( 3 FDA reports)
BLOOD UREA DECREASED ( 3 FDA reports)
BREAKTHROUGH PAIN ( 3 FDA reports)
BURKITT'S LYMPHOMA ( 3 FDA reports)
CANDIDA PNEUMONIA ( 3 FDA reports)
CAPILLARY PERMEABILITY INCREASED ( 3 FDA reports)
CARBON DIOXIDE INCREASED ( 3 FDA reports)
CARDIOVASCULAR DISORDER ( 3 FDA reports)
CATHETER SITE HAEMORRHAGE ( 3 FDA reports)
CELLULITIS GANGRENOUS ( 3 FDA reports)
CEREBRAL ISCHAEMIA ( 3 FDA reports)
CHLOROMA ( 3 FDA reports)
CHOLANGITIS SUPPURATIVE ( 3 FDA reports)
CHOLECYSTITIS ACUTE ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
CLONIC CONVULSION ( 3 FDA reports)
CLOSTRIDIUM COLITIS ( 3 FDA reports)
COLLAPSE OF LUNG ( 3 FDA reports)
CORYNEBACTERIUM SEPSIS ( 3 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 3 FDA reports)
DEAFNESS BILATERAL ( 3 FDA reports)
DEAFNESS UNILATERAL ( 3 FDA reports)
DRUG DISPENSING ERROR ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
DYSPLASIA ( 3 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
EYE PRURITUS ( 3 FDA reports)
FEBRILE CONVULSION ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
GASTROINTESTINAL TOXICITY ( 3 FDA reports)
GLOMERULONEPHROPATHY ( 3 FDA reports)
HAEMATOTOXICITY ( 3 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HEPATIC FIBROSIS ( 3 FDA reports)
HEPATIC NECROSIS ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HEPATITIS E ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HYDROCELE ( 3 FDA reports)
HYPERLIPIDAEMIA ( 3 FDA reports)
HYPERREFLEXIA ( 3 FDA reports)
HYPERTHYROIDISM ( 3 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 3 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 3 FDA reports)
INTESTINAL ISCHAEMIA ( 3 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 3 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 3 FDA reports)
KERATITIS ( 3 FDA reports)
LIP EROSION ( 3 FDA reports)
LIVER INJURY ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
MEDULLOBLASTOMA RECURRENT ( 3 FDA reports)
MENINGITIS BACTERIAL ( 3 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 3 FDA reports)
MICROSPORIDIA INFECTION ( 3 FDA reports)
MONOCYTE COUNT DECREASED ( 3 FDA reports)
MULTIPLE MYELOMA ( 3 FDA reports)
MYELOCYTE PERCENTAGE INCREASED ( 3 FDA reports)
MYELOPATHY ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
NEOPLASM RECURRENCE ( 3 FDA reports)
NEPHROTIC SYNDROME ( 3 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 3 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 3 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 3 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 3 FDA reports)
OESOPHAGEAL STENOSIS ( 3 FDA reports)
OSTEOMYELITIS ( 3 FDA reports)
PANCREATIC ENLARGEMENT ( 3 FDA reports)
PARAPLEGIA ( 3 FDA reports)
PARTIAL SEIZURES ( 3 FDA reports)
PEARSON'S SYNDROME ( 3 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 3 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 3 FDA reports)
PROTHROMBIN TIME SHORTENED ( 3 FDA reports)
PURULENCE ( 3 FDA reports)
QUADRIPLEGIA ( 3 FDA reports)
RALES ( 3 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 3 FDA reports)
SCAB ( 3 FDA reports)
SELF-MEDICATION ( 3 FDA reports)
SEPSIS SYNDROME ( 3 FDA reports)
SINUS DISORDER ( 3 FDA reports)
SKIN ATROPHY ( 3 FDA reports)
SKIN CANDIDA ( 3 FDA reports)
SKIN EROSION ( 3 FDA reports)
SKIN HYPERPIGMENTATION ( 3 FDA reports)
SKIN NODULE ( 3 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 3 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 3 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 3 FDA reports)
STRESS ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
SURGICAL PROCEDURE REPEATED ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
THYROID NEOPLASM ( 3 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO DECREASED ( 3 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 3 FDA reports)
VAGINAL CELLULITIS ( 3 FDA reports)
VASCULITIS CEREBRAL ( 3 FDA reports)
VASOSPASM ( 3 FDA reports)
VIRAL RASH ( 3 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
ABSCESS FUNGAL ( 2 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ACUTE SINUSITIS ( 2 FDA reports)
ADENOVIRAL HEPATITIS ( 2 FDA reports)
AIDS ENCEPHALOPATHY ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
APPENDICITIS ( 2 FDA reports)
ARGININOSUCCINATE SYNTHETASE DEFICIENCY ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 2 FDA reports)
BACTERIA STOOL IDENTIFIED ( 2 FDA reports)
BETA 2 MICROGLOBULIN DECREASED ( 2 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 2 FDA reports)
BLAST CELL COUNT INCREASED ( 2 FDA reports)
BLASTOMYCOSIS ( 2 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 2 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD MAGNESIUM INCREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BONE EROSION ( 2 FDA reports)
BREATH ODOUR ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CANDIDA TEST POSITIVE ( 2 FDA reports)
CARDIAC ENZYMES INCREASED ( 2 FDA reports)
CARDIAC FAILURE CHRONIC ( 2 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 2 FDA reports)
CEREBELLAR INFARCTION ( 2 FDA reports)
CEREBRAL DISORDER ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA TRANSFORMATION ( 2 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 2 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 2 FDA reports)
CITROBACTER SEPSIS ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CRYING ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
CYSTITIS HAEMORRHAGIC ( 2 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DEVICE INTERACTION ( 2 FDA reports)
DEVICE OCCLUSION ( 2 FDA reports)
DIABETIC KETOACIDOTIC HYPERGLYCAEMIC COMA ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG LEVEL DECREASED ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
EFFUSION ( 2 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
EMBOLIC STROKE ( 2 FDA reports)
ENCEPHALITIS FUNGAL ( 2 FDA reports)
ENCEPHALITIS HERPES ( 2 FDA reports)
ENCEPHALITIS TOXIC ( 2 FDA reports)
ENDOPHTHALMITIS ( 2 FDA reports)
ENTEROBACTER TEST POSITIVE ( 2 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 2 FDA reports)
ENTEROCOLITIS BACTERIAL ( 2 FDA reports)
ERYTHROBLAST COUNT INCREASED ( 2 FDA reports)
ESCHERICHIA BACTERAEMIA ( 2 FDA reports)
FACTOR V DEFICIENCY ( 2 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 2 FDA reports)
FULL BLOOD COUNT DECREASED ( 2 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 2 FDA reports)
GALLBLADDER POLYP ( 2 FDA reports)
GALLOP RHYTHM PRESENT ( 2 FDA reports)
GANGRENE ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE IN LIVER ( 2 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMOGLOBIN ABNORMAL ( 2 FDA reports)
HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMOGLOBINURIA ( 2 FDA reports)
HAEMORRHAGIC STROKE ( 2 FDA reports)
HEART SOUNDS ABNORMAL ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATIC ISCHAEMIA ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HIV INFECTION ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPERCHLORAEMIA ( 2 FDA reports)
HYPOAESTHESIA FACIAL ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 2 FDA reports)
IMMUNODEFICIENCY ( 2 FDA reports)
IMPATIENCE ( 2 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INFUSION SITE RASH ( 2 FDA reports)
INJECTION SITE EXTRAVASATION ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
JEJUNITIS ( 2 FDA reports)
KIDNEY ENLARGEMENT ( 2 FDA reports)
KIDNEY INFECTION ( 2 FDA reports)
KLEBSIELLA SEPSIS ( 2 FDA reports)
KLEBSIELLA TEST POSITIVE ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LABORATORY TEST INTERFERENCE ( 2 FDA reports)
LACTOBACILLUS INFECTION ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LARYNGITIS ( 2 FDA reports)
LARYNGOSPASM ( 2 FDA reports)
LEFT ATRIAL DILATATION ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LEISHMANIASIS ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
LIVER TRANSPLANT ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LOGORRHOEA ( 2 FDA reports)
LONG QT SYNDROME ( 2 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 2 FDA reports)
LUNG TRANSPLANT REJECTION ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MENINGIOMA ( 2 FDA reports)
MENINGITIS LISTERIA ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
METABOLIC ALKALOSIS ( 2 FDA reports)
METABOLIC SYNDROME ( 2 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 2 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 2 FDA reports)
MITOCHONDRIAL TOXICITY ( 2 FDA reports)
MITRAL VALVE DISEASE ( 2 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
NEONATAL DISORDER ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
OPPORTUNISTIC INFECTION ( 2 FDA reports)
OPTIC NERVE DISORDER ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
ORGAN FAILURE ( 2 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 2 FDA reports)
OSTEOMYELITIS FUNGAL ( 2 FDA reports)
OSTEOPENIA ( 2 FDA reports)
PALLANAESTHESIA ( 2 FDA reports)
PALMAR ERYTHEMA ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERITONEAL NECROSIS ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PHLEBOTHROMBOSIS ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PLEURAL INFECTION ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 2 FDA reports)
PNEUMONIA TOXOPLASMAL ( 2 FDA reports)
POSTURING ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 2 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PULMONARY VASCULAR DISORDER ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
PYELOCALIECTASIS ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
RENAL ABSCESS ( 2 FDA reports)
RESPIRATORY ALKALOSIS ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RETCHING ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
RIGHT ATRIAL DILATATION ( 2 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SARCOIDOSIS ( 2 FDA reports)
SCAR ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
SCROTAL ULCER ( 2 FDA reports)
SENSORIMOTOR DISORDER ( 2 FDA reports)
SEPTIC ENCEPHALOPATHY ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SOFT TISSUE INFECTION ( 2 FDA reports)
SPINAL DISORDER ( 2 FDA reports)
SPUTUM CULTURE POSITIVE ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 2 FDA reports)
SUBDURAL HAEMORRHAGE ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
TORTICOLLIS ( 2 FDA reports)
TRACHEAL HAEMORRHAGE ( 2 FDA reports)
TRACHEOBRONCHITIS ( 2 FDA reports)
TRANSFUSION REACTION ( 2 FDA reports)
TRANSPLANT FAILURE ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
ULCER ( 2 FDA reports)
URINARY CASTS ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
URINARY SEDIMENT ABNORMAL ( 2 FDA reports)
URINARY SEDIMENT PRESENT ( 2 FDA reports)
URINE POTASSIUM ABNORMAL ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VARICELLA ( 2 FDA reports)
VASCULAR PSEUDOANEURYSM RUPTURED ( 2 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
VITH NERVE PARALYSIS ( 2 FDA reports)
WOUND ( 2 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL SYMPTOM ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACINETOBACTER TEST POSITIVE ( 1 FDA reports)
ACOUSTIC STIMULATION TESTS ABNORMAL ( 1 FDA reports)
ACUTE BIPHENOTYPIC LEUKAEMIA ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADRENAL CORTEX NECROSIS ( 1 FDA reports)
AGITATION NEONATAL ( 1 FDA reports)
AGONAL DEATH STRUGGLE ( 1 FDA reports)
AMERICAN TRYPANOSOMIASIS ( 1 FDA reports)
AMINO ACID LEVEL INCREASED ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APNOEIC ATTACK ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
AXILLARY VEIN THROMBOSIS ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
BILE DUCT NECROSIS ( 1 FDA reports)
BILIARY CIRRHOSIS PRIMARY ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BIOPSY BRAIN ABNORMAL ( 1 FDA reports)
BK VIRUS INFECTION ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD BETA-D-GLUCAN DECREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CHOLESTEROL ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BONE MARROW OEDEMA ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRADYPNOEA ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN MASS ( 1 FDA reports)
BRAIN MIDLINE SHIFT ( 1 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BURKITT'S LEUKAEMIA ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CAMPYLOBACTER INFECTION ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CATHETER CULTURE POSITIVE ( 1 FDA reports)
CATHETER SITE ERYTHEMA ( 1 FDA reports)
CATHETER SITE INFLAMMATION ( 1 FDA reports)
CATHETER SITE PAIN ( 1 FDA reports)
CAUDA EQUINA SYNDROME ( 1 FDA reports)
CD4/CD8 RATIO INCREASED ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM VIRAL INFECTION ( 1 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLANGITIS SCLEROSING ( 1 FDA reports)
CHOLURIA ( 1 FDA reports)
CHORIOAMNIONITIS ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COCCIDIOIDOMYCOSIS ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CORONARY ARTERY ANEURYSM ( 1 FDA reports)
CORYNEBACTERIUM TEST POSITIVE ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 1 FDA reports)
CRYSTAL URINE ( 1 FDA reports)
CSF GLUCOSE DECREASED ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYTOGENETIC ABNORMALITY ( 1 FDA reports)
CYTOKINE RELEASE SYNDROME ( 1 FDA reports)
DEATH NEONATAL ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DEVICE MIGRATION ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DISSEMINATED CRYPTOCOCCOSIS ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DISTRIBUTIVE SHOCK ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENDOCRINE DISORDER ( 1 FDA reports)
ENGRAFT FAILURE ( 1 FDA reports)
ENTEROBACTER BACTERAEMIA ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE INFECTION FUNGAL ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FOAMING AT MOUTH ( 1 FDA reports)
FOETAL GROWTH RESTRICTION ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
FUNGUS CULTURE POSITIVE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL MUCOSITIS ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRANULOCYTES ABNORMAL ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMODIALYSIS-INDUCED SYMPTOM ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HELMINTHIC INFECTION ( 1 FDA reports)
HEPATIC ARTERY ANEURYSM ( 1 FDA reports)
HEPATIC HAEMATOMA ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATIC INFECTION FUNGAL ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS GRANULOMATOUS ( 1 FDA reports)
HERPES OESOPHAGITIS ( 1 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
HUMAN POLYOMAVIRUS INFECTION ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERCAPNIC ENCEPHALOPATHY ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPERVISCOSITY SYNDROME ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTONIC-HYPORESPONSIVE EPISODE ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IIIRD NERVE PARALYSIS ( 1 FDA reports)
ILEOSTOMY ( 1 FDA reports)
IMMEDIATE POST-INJECTION REACTION ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INFUSION SITE INFLAMMATION ( 1 FDA reports)
INFUSION SITE SWELLING ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INJURY ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL HAEMATOMA ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
IVTH NERVE PARALYSIS ( 1 FDA reports)
JARISCH-HERXHEIMER REACTION ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
JUVENILE ARTHRITIS ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARYNGEAL CANCER ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOSS OF PROPRIOCEPTION ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MEDIASTINUM NEOPLASM ( 1 FDA reports)
MEGACOLON ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENINGITIS FUNGAL ( 1 FDA reports)
MENINGOCOCCAL INFECTION ( 1 FDA reports)
METASTASES TO BONE MARROW ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTASES TO PERIPHERAL VASCULAR SYSTEM ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOCUTANEOUS RASH ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE MASS ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYELOID LEUKAEMIA ( 1 FDA reports)
MYOCARDIAL HAEMORRHAGE ( 1 FDA reports)
MYOPATHY STEROID ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NECROTISING RETINITIS ( 1 FDA reports)
NEONATAL MULTI-ORGAN FAILURE ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUROPATHIC PAIN ( 1 FDA reports)
NEUTROPENIC INFECTION ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OCCULT BLOOD ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OESOPHAGEAL DILATATION ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
OPTIC NERVE INFARCTION ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PAPILLOMA VIRAL INFECTION ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PELVIC INFECTION ( 1 FDA reports)
PERICARDITIS FUNGAL ( 1 FDA reports)
PERICARDITIS INFECTIVE ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 1 FDA reports)
PNEUMONIA INFLUENZAL ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PNEUMONIA PARAINFLUENZAE VIRAL ( 1 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
PNEUMOPERICARDIUM ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 1 FDA reports)
POOR PERSONAL HYGIENE ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
POSTOPERATIVE RENAL FAILURE ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROPOFOL INFUSION SYNDROME ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDOBULBAR PALSY ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY COCCIDIOIDES ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULMONARY SEPSIS ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RECALL PHENOMENON ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RENAL AMYLOIDOSIS ( 1 FDA reports)
RENAL FAILURE NEONATAL ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RETINAL INFILTRATES ( 1 FDA reports)
RETINAL INJURY ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SCROTAL PAIN ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SERRATIA SEPSIS ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN TEST NEGATIVE ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SMALL INTESTINE ULCER ( 1 FDA reports)
SPLENIC ABSCESS ( 1 FDA reports)
SPLENIC RUPTURE ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
STOMATITIS NECROTISING ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBCUTANEOUS NODULE ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TOXIC SHOCK SYNDROME ( 1 FDA reports)
TRACHEOMALACIA ( 1 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
UROBILIN URINE PRESENT ( 1 FDA reports)
VARICELLA ZOSTER VIRUS SEROLOGY POSITIVE ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VIRAL DNA TEST POSITIVE ( 1 FDA reports)
VIRUS URINE TEST POSITIVE ( 1 FDA reports)
VISCERAL LEISHMANIASIS ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITREOUS OPACITIES ( 1 FDA reports)
WALDENSTROM'S MACROGLOBULINAEMIA ( 1 FDA reports)
WEGENER'S GRANULOMATOSIS ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use