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

PYREXIA ( 87 FDA reports)
NEUTROPENIA ( 83 FDA reports)
RENAL IMPAIRMENT ( 63 FDA reports)
MULTI-ORGAN FAILURE ( 59 FDA reports)
SEPSIS ( 59 FDA reports)
PNEUMONIA ( 52 FDA reports)
FEBRILE NEUTROPENIA ( 50 FDA reports)
SEPTIC SHOCK ( 49 FDA reports)
DYSPNOEA ( 46 FDA reports)
HYPOTENSION ( 45 FDA reports)
PANCYTOPENIA ( 45 FDA reports)
THROMBOCYTOPENIA ( 45 FDA reports)
METABOLIC ACIDOSIS ( 35 FDA reports)
RENAL FAILURE ACUTE ( 31 FDA reports)
ATRIAL FIBRILLATION ( 28 FDA reports)
DIARRHOEA ( 28 FDA reports)
HEADACHE ( 28 FDA reports)
INFECTION ( 28 FDA reports)
PERICARDITIS ( 28 FDA reports)
NAUSEA ( 26 FDA reports)
VOMITING ( 26 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 24 FDA reports)
BONE MARROW FAILURE ( 24 FDA reports)
PLATELET COUNT DECREASED ( 24 FDA reports)
DEATH ( 23 FDA reports)
NEUTROPENIC SEPSIS ( 23 FDA reports)
CARDIAC ARREST ( 22 FDA reports)
RESPIRATORY FAILURE ( 22 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 21 FDA reports)
DISEASE PROGRESSION ( 21 FDA reports)
CEREBRAL HAEMORRHAGE ( 20 FDA reports)
RENAL FAILURE ( 20 FDA reports)
ANAEMIA ( 19 FDA reports)
FATIGUE ( 19 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 17 FDA reports)
GRAFT VERSUS HOST DISEASE ( 17 FDA reports)
HYPOPHOSPHATAEMIA ( 17 FDA reports)
ABDOMINAL PAIN ( 16 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 16 FDA reports)
CARDIAC FAILURE ( 16 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 16 FDA reports)
DRUG TOXICITY ( 15 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 15 FDA reports)
BACTERAEMIA ( 14 FDA reports)
CHILLS ( 14 FDA reports)
DRUG INTERACTION ( 14 FDA reports)
HYPOXIA ( 14 FDA reports)
TUMOUR LYSIS SYNDROME ( 14 FDA reports)
CAECITIS ( 13 FDA reports)
STAPHYLOCOCCAL INFECTION ( 13 FDA reports)
TACHYCARDIA ( 13 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 12 FDA reports)
ASTHENIA ( 12 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 12 FDA reports)
COUGH ( 12 FDA reports)
DEHYDRATION ( 12 FDA reports)
FUNGAL INFECTION ( 12 FDA reports)
HAEMOGLOBIN DECREASED ( 12 FDA reports)
HYPOALBUMINAEMIA ( 12 FDA reports)
RASH ( 12 FDA reports)
ACUTE RESPIRATORY FAILURE ( 11 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
CHEST PAIN ( 11 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 11 FDA reports)
MYOCARDIAL INFARCTION ( 11 FDA reports)
PULMONARY HAEMORRHAGE ( 11 FDA reports)
RESPIRATORY DISTRESS ( 11 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 11 FDA reports)
DRUG INEFFECTIVE ( 10 FDA reports)
HYPOCALCAEMIA ( 10 FDA reports)
JAUNDICE ( 10 FDA reports)
MYELODYSPLASTIC SYNDROME ( 10 FDA reports)
PAIN ( 10 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 10 FDA reports)
SOMNOLENCE ( 10 FDA reports)
URINARY INCONTINENCE ( 10 FDA reports)
ENCEPHALITIS ( 9 FDA reports)
HEPATIC ENZYME INCREASED ( 9 FDA reports)
HEPATIC FAILURE ( 9 FDA reports)
INTERSTITIAL LUNG DISEASE ( 9 FDA reports)
INTRACRANIAL HYPOTENSION ( 9 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 9 FDA reports)
LUNG DISORDER ( 9 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 9 FDA reports)
MALAISE ( 9 FDA reports)
PULMONARY OEDEMA ( 9 FDA reports)
TACHYPNOEA ( 9 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 9 FDA reports)
TRANSAMINASES INCREASED ( 9 FDA reports)
ABDOMINAL DISTENSION ( 8 FDA reports)
ACIDOSIS ( 8 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 8 FDA reports)
ALANINE AMINOTRANSFERASE ( 8 FDA reports)
ALKALOSIS ( 8 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 8 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 8 FDA reports)
BLOOD BILIRUBIN ( 8 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 8 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 8 FDA reports)
ENCEPHALOPATHY ( 8 FDA reports)
EPISTAXIS ( 8 FDA reports)
LEUKOPENIA ( 8 FDA reports)
LOSS OF CONSCIOUSNESS ( 8 FDA reports)
LUNG INFECTION ( 8 FDA reports)
LUNG INFILTRATION ( 8 FDA reports)
MYELOBLAST COUNT INCREASED ( 8 FDA reports)
OEDEMA PERIPHERAL ( 8 FDA reports)
ORAL HERPES ( 8 FDA reports)
PARAPLEGIA ( 8 FDA reports)
STOMATITIS ( 8 FDA reports)
URINARY TRACT INFECTION ( 8 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 7 FDA reports)
ASPERGILLOSIS ( 7 FDA reports)
BLOOD POTASSIUM DECREASED ( 7 FDA reports)
CONDITION AGGRAVATED ( 7 FDA reports)
CONVULSION ( 7 FDA reports)
DYSARTHRIA ( 7 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 7 FDA reports)
ERYTHEMA MULTIFORME ( 7 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 7 FDA reports)
HAEMOLYSIS ( 7 FDA reports)
HEPATOTOXICITY ( 7 FDA reports)
HYPERBILIRUBINAEMIA ( 7 FDA reports)
MUCOSAL INFLAMMATION ( 7 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
NEUROTOXICITY ( 7 FDA reports)
OXYGEN SATURATION DECREASED ( 7 FDA reports)
PARAPARESIS ( 7 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 7 FDA reports)
STEM CELL TRANSPLANT ( 7 FDA reports)
SUBDURAL HAEMATOMA ( 7 FDA reports)
URINE OUTPUT DECREASED ( 7 FDA reports)
WEIGHT DECREASED ( 7 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 6 FDA reports)
APLASIA PURE RED CELL ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 6 FDA reports)
BLAST CELL COUNT DECREASED ( 6 FDA reports)
BLOOD IRON INCREASED ( 6 FDA reports)
BONE MARROW TRANSPLANT ( 6 FDA reports)
BRONCHOPNEUMONIA ( 6 FDA reports)
CELLULITIS ORBITAL ( 6 FDA reports)
CLOSTRIDIAL INFECTION ( 6 FDA reports)
CONFUSIONAL STATE ( 6 FDA reports)
DRUG RESISTANCE ( 6 FDA reports)
FULL BLOOD COUNT DECREASED ( 6 FDA reports)
HEPATIC VEIN OCCLUSION ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
LEUKOCYTOSIS ( 6 FDA reports)
MELAENA ( 6 FDA reports)
ORAL DISORDER ( 6 FDA reports)
PANCREATITIS ACUTE ( 6 FDA reports)
PNEUMONIA BACTERIAL ( 6 FDA reports)
RHABDOMYOLYSIS ( 6 FDA reports)
SHOCK ( 6 FDA reports)
SINUS CONGESTION ( 6 FDA reports)
SINUS DISORDER ( 6 FDA reports)
WERNICKE'S ENCEPHALOPATHY ( 6 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 5 FDA reports)
BLOOD CULTURE POSITIVE ( 5 FDA reports)
BONE MARROW DEPRESSION ( 5 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 5 FDA reports)
CEREBELLAR ATAXIA ( 5 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 5 FDA reports)
COLOSTOMY ( 5 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 5 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 5 FDA reports)
DYSPEPSIA ( 5 FDA reports)
ENTEROCOCCAL SEPSIS ( 5 FDA reports)
FALL ( 5 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 5 FDA reports)
FLUID OVERLOAD ( 5 FDA reports)
GUILLAIN-BARRE SYNDROME ( 5 FDA reports)
HERPES SIMPLEX ( 5 FDA reports)
IDIOPATHIC PNEUMONIA SYNDROME ( 5 FDA reports)
ISCHAEMIC STROKE ( 5 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 5 FDA reports)
LOCALISED OEDEMA ( 5 FDA reports)
LYMPHADENOPATHY ( 5 FDA reports)
MUCORMYCOSIS ( 5 FDA reports)
MYDRIASIS ( 5 FDA reports)
NEUTROPHIL COUNT DECREASED ( 5 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
PURPURA ( 5 FDA reports)
RECTAL ABSCESS ( 5 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
TENOSYNOVITIS ( 5 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 5 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 4 FDA reports)
ANAL ABSCESS ( 4 FDA reports)
ANURIA ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
BACTERIAL INFECTION ( 4 FDA reports)
BLOOD ALBUMIN DECREASED ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
CATARACT ( 4 FDA reports)
CEREBELLAR SYNDROME ( 4 FDA reports)
CEREBRAL ISCHAEMIA ( 4 FDA reports)
CHOLESTASIS ( 4 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
COAGULOPATHY ( 4 FDA reports)
CYTOGENETIC ABNORMALITY ( 4 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DERMATITIS EXFOLIATIVE ( 4 FDA reports)
DEVICE RELATED INFECTION ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
ENTEROCOCCAL INFECTION ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
HEPATOMEGALY ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 4 FDA reports)
INFUSION RELATED REACTION ( 4 FDA reports)
INTESTINAL HAEMORRHAGE ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
LOBAR PNEUMONIA ( 4 FDA reports)
MEDICAL DEVICE COMPLICATION ( 4 FDA reports)
MUSCLE DISORDER ( 4 FDA reports)
MYELOPATHY ( 4 FDA reports)
NOCARDIOSIS ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
POST PROCEDURAL COMPLICATION ( 4 FDA reports)
PULMONARY TOXICITY ( 4 FDA reports)
RESPIRATORY TRACT INFECTION ( 4 FDA reports)
SUBDURAL HAEMORRHAGE ( 4 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 4 FDA reports)
URINARY RETENTION ( 4 FDA reports)
VAGINAL DISCHARGE ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
AGITATION ( 3 FDA reports)
ALLOGENIC BONE MARROW TRANSPLANTATION THERAPY ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ASCITES ( 3 FDA reports)
ASPERGILLOMA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BACTERIA STOOL IDENTIFIED ( 3 FDA reports)
BACTERIAL DIARRHOEA ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
BRAIN HERNIATION ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
BREATH SOUNDS ABNORMAL ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CARDIAC TAMPONADE ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CHEMOTHERAPEUTIC DRUG LEVEL INCREASED ( 3 FDA reports)
COLITIS ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
CREPITATIONS ( 3 FDA reports)
CYTOGENETIC ANALYSIS ABNORMAL ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DIASTOLIC DYSFUNCTION ( 3 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 3 FDA reports)
DISEASE RECURRENCE ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 3 FDA reports)
DYSAESTHESIA ( 3 FDA reports)
ENTEROBACTER BACTERAEMIA ( 3 FDA reports)
FUNGUS CULTURE POSITIVE ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
GINGIVAL BLEEDING ( 3 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
HYPERPYREXIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
KLEBSIELLA INFECTION ( 3 FDA reports)
LEUKAEMIA ( 3 FDA reports)
LEUKAEMIC INFILTRATION BRAIN ( 3 FDA reports)
LUNG CONSOLIDATION ( 3 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 3 FDA reports)
MAJOR DEPRESSION ( 3 FDA reports)
MARROW HYPERPLASIA ( 3 FDA reports)
MONOPLEGIA ( 3 FDA reports)
MYELOCYTOSIS ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 3 FDA reports)
PNEUMONIA FUNGAL ( 3 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 3 FDA reports)
PNEUMOTHORAX ( 3 FDA reports)
PROCEDURAL COMPLICATION ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
PULMONARY SEQUESTRATION ( 3 FDA reports)
PULSE ABSENT ( 3 FDA reports)
PUPILS UNEQUAL ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
SPLENOMEGALY ( 3 FDA reports)
T-CELL LYMPHOMA ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
TOXIC ENCEPHALOPATHY ( 3 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 3 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 3 FDA reports)
VENOOCCLUSIVE DISEASE ( 3 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 3 FDA reports)
VENTRICULAR DYSFUNCTION ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
WOUND INFECTION ( 3 FDA reports)
ACTINOMYCOTIC PULMONARY INFECTION ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE BIPHENOTYPIC LEUKAEMIA ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 2 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
APLASIA ( 2 FDA reports)
APNOEA ( 2 FDA reports)
APPENDICITIS ( 2 FDA reports)
APRAXIA ( 2 FDA reports)
ATRIAL TACHYCARDIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
AV DISSOCIATION ( 2 FDA reports)
B-LYMPHOCYTE ABNORMALITIES ( 2 FDA reports)
BLAST CELL CRISIS ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CARDIOTOXICITY ( 2 FDA reports)
CAROTID ARTERY OCCLUSION ( 2 FDA reports)
CATHETER SITE CELLULITIS ( 2 FDA reports)
CATHETER SITE NECROSIS ( 2 FDA reports)
CAUDA EQUINA SYNDROME ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CEREBRAL DISORDER ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
COMA ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSPHASIA ( 2 FDA reports)
EMBOLISM ARTERIAL ( 2 FDA reports)
ENCEPHALITIS HERPES ( 2 FDA reports)
ENGRAFTMENT SYNDROME ( 2 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
ERYTHEMA OF EYELID ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
EYE DISCHARGE ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FACIAL PARESIS ( 2 FDA reports)
FAILURE TO THRIVE ( 2 FDA reports)
FEBRILE INFECTION ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC INFARCTION ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
HYPOVOLAEMIC SHOCK ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 2 FDA reports)
INFLAMMATORY MYOFIBROBLASTIC TUMOUR ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 2 FDA reports)
INTUBATION ( 2 FDA reports)
IRON OVERLOAD ( 2 FDA reports)
LEAD DISLODGEMENT ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LEUKAEMIC INFILTRATION EXTRAMEDULLARY ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LIVER ABSCESS ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MEGACOLON ( 2 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PERIORBITAL CELLULITIS ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
PUNCTURE SITE INFECTION ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
SPLENIC INFARCTION ( 2 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
TERMINAL STATE ( 2 FDA reports)
THALAMUS HAEMORRHAGE ( 2 FDA reports)
TOOTHACHE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VASOSPASM ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
ZYGOMYCOSIS ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACTERIAL DISEASE CARRIER ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLAST CELL PROLIFERATION ( 1 FDA reports)
BLAST CELLS ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD BRAIN BARRIER DEFECT ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BONE DEBRIDEMENT ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE INFARCTION ( 1 FDA reports)
BONE MARROW LEUKAEMIC CELL INFILTRATION ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BURKITT'S LYMPHOMA STAGE III ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ASPERGILLOSIS ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CHROMOSOME ANALYSIS ABNORMAL ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORTICAL LAMINAR NECROSIS ( 1 FDA reports)
CRANIOTOMY ( 1 FDA reports)
CRYING ( 1 FDA reports)
CRYSTAL URINE PRESENT ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DENERVATION ATROPHY ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATITIS EXFOLIATIVE GENERALISED ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTEROBACTER TEST POSITIVE ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EYE INFECTION FUNGAL ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEAR OF DISEASE ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC MUCOSAL LESION ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL MUCOSITIS ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 1 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOPHILUS TEST POSITIVE ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC VEIN DILATATION ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HEPATOSPLENIC CANDIDIASIS ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
IIIRD NERVE PARALYSIS ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION SITE BURNING ( 1 FDA reports)
INTERTRIGO ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INTRASPINAL ABSCESS ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
JOINT DESTRUCTION ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MASS ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MESANGIOPROLIFERATIVE GLOMERULONEPHRITIS ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METASTASES TO BONE MARROW ( 1 FDA reports)
METASTASES TO STOMACH ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MUSCLE MASS ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYCOSIS FUNGOIDES RECURRENT ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NEUROLOGIC NEGLECT SYNDROME ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
ORCHIDECTOMY ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEOMYELITIS FUNGAL ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 1 FDA reports)
PERICARDIAL RUB ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMATOSIS CYSTOIDES INTESTINALIS ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONIA HERPES VIRAL ( 1 FDA reports)
PNEUMONIA INFLUENZAL ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 1 FDA reports)
POST PROCEDURAL DIARRHOEA ( 1 FDA reports)
POST PROCEDURAL VOMITING ( 1 FDA reports)
PRECURSOR T-LYMPHOBLASTIC LYMPHOMA/LEUKAEMIA ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PROSTATIC MASS ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULMONARY VASCULAR RESISTANCE ABNORMALITY ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RADICULOPATHY ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH FOLLICULAR ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
REFRACTORY ANAEMIA ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETINAL OEDEMA ( 1 FDA reports)
RETINOIC ACID SYNDROME ( 1 FDA reports)
SALIVARY GLAND MASS ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SHIFT TO THE LEFT ( 1 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SLEEP DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SMALL INTESTINAL STENOSIS ( 1 FDA reports)
SMALL INTESTINE ULCER ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC ABSCESS ( 1 FDA reports)
SPLENIC NECROSIS ( 1 FDA reports)
SPLENIC RUPTURE ( 1 FDA reports)
STOMATITIS NECROTISING ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBCUTANEOUS NODULE ( 1 FDA reports)
SUBDURAL HYGROMA ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
SYSTEMIC MYCOSIS ( 1 FDA reports)
SYSTEMIC SCLEROSIS ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONSILLECTOMY ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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