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

GRAFT VERSUS HOST DISEASE ( 27 FDA reports)
PYREXIA ( 25 FDA reports)
MULTI-ORGAN FAILURE ( 19 FDA reports)
PANCYTOPENIA ( 19 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 18 FDA reports)
APLASTIC ANAEMIA ( 16 FDA reports)
INFECTION ( 16 FDA reports)
SEPSIS ( 16 FDA reports)
PNEUMONIA ( 15 FDA reports)
BONE MARROW FAILURE ( 14 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 14 FDA reports)
DISEASE PROGRESSION ( 13 FDA reports)
STEM CELL TRANSPLANT ( 13 FDA reports)
THROMBOCYTOPENIA ( 13 FDA reports)
BLOOD CREATININE INCREASED ( 12 FDA reports)
DIARRHOEA ( 12 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 12 FDA reports)
HEPATIC FAILURE ( 12 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 12 FDA reports)
HEPATITIS ( 12 FDA reports)
LIVER TRANSPLANT ( 12 FDA reports)
MYELODYSPLASTIC SYNDROME ( 12 FDA reports)
RENAL FAILURE ( 11 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 10 FDA reports)
BONE MARROW DISORDER ( 10 FDA reports)
DISSEMINATED TUBERCULOSIS ( 10 FDA reports)
RENAL IMPAIRMENT ( 10 FDA reports)
RESPIRATORY FAILURE ( 10 FDA reports)
ABDOMINAL INFECTION ( 9 FDA reports)
ABDOMINAL PAIN ( 9 FDA reports)
CHROMOSOME ABNORMALITY ( 9 FDA reports)
COMA HEPATIC ( 9 FDA reports)
HAEMOSIDEROSIS ( 9 FDA reports)
HEPATIC ATROPHY ( 9 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 9 FDA reports)
RENAL FAILURE ACUTE ( 9 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 9 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 8 FDA reports)
FEBRILE NEUTROPENIA ( 8 FDA reports)
HAEMODIALYSIS ( 8 FDA reports)
NEUTROPENIA ( 8 FDA reports)
TRANSPLANT REJECTION ( 8 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 7 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 7 FDA reports)
BLOOD PRESSURE INCREASED ( 7 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 7 FDA reports)
CARDIAC FAILURE ( 7 FDA reports)
CONVULSION ( 7 FDA reports)
DRUG INEFFECTIVE ( 7 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 7 FDA reports)
AORTIC DISSECTION ( 6 FDA reports)
BK VIRUS INFECTION ( 6 FDA reports)
GRAND MAL CONVULSION ( 6 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 6 FDA reports)
LUNG INFILTRATION ( 6 FDA reports)
LYMPHOPENIA ( 6 FDA reports)
STAPHYLOCOCCAL INFECTION ( 6 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 6 FDA reports)
ZYGOMYCOSIS ( 6 FDA reports)
ABDOMINAL TENDERNESS ( 5 FDA reports)
BACTERIAL INFECTION ( 5 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 5 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
INFLAMMATION ( 5 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 5 FDA reports)
NEPHROPATHY TOXIC ( 5 FDA reports)
PAIN ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
SEPTIC SHOCK ( 5 FDA reports)
VOMITING ( 5 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ASCITES ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 4 FDA reports)
CANDIDIASIS ( 4 FDA reports)
CARPAL TUNNEL SYNDROME ( 4 FDA reports)
CYSTITIS HAEMORRHAGIC ( 4 FDA reports)
DEATH ( 4 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
NODULE ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
PANCREATITIS ACUTE ( 4 FDA reports)
PERITONITIS ( 4 FDA reports)
PROTEINURIA ( 4 FDA reports)
PSEUDOMONAS INFECTION ( 4 FDA reports)
RASH ( 4 FDA reports)
STOMATITIS ( 4 FDA reports)
SWELLING ( 4 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 4 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 3 FDA reports)
APLASIA PURE RED CELL ( 3 FDA reports)
ASPERGILLOSIS ( 3 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 3 FDA reports)
BLOOD AMYLASE INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CHEST X-RAY ABNORMAL ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 3 FDA reports)
DEMYELINATION ( 3 FDA reports)
DIFFUSE AXONAL INJURY ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
GASTROENTERITIS ADENOVIRUS ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HEPATIC NECROSIS ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 3 FDA reports)
ISCHAEMIC STROKE ( 3 FDA reports)
KLEBSIELLA SEPSIS ( 3 FDA reports)
LEUKAEMIA RECURRENT ( 3 FDA reports)
LEUKOENCEPHALOPATHY ( 3 FDA reports)
LIGAMENT DISORDER ( 3 FDA reports)
LIPASE INCREASED ( 3 FDA reports)
LIVER TRANSPLANT REJECTION ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 3 FDA reports)
MOTOR DYSFUNCTION ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
NEPHROTIC SYNDROME ( 3 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 3 FDA reports)
OCCULT BLOOD POSITIVE ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
PULMONARY FIBROSIS ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
RETICULOCYTE COUNT DECREASED ( 3 FDA reports)
SENSORY LOSS ( 3 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 3 FDA reports)
STREPTOCOCCAL INFECTION ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
TACHYPNOEA ( 3 FDA reports)
TOXOPLASMOSIS ( 3 FDA reports)
ABDOMINAL MASS ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ADENOVIRUS INFECTION ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ANURIA ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BACILLUS INFECTION ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BILE DUCT CANCER ( 2 FDA reports)
CANDIDA SEPSIS ( 2 FDA reports)
CAPILLARY LEAK SYNDROME ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CLEFT LIP ( 2 FDA reports)
CLEFT PALATE ( 2 FDA reports)
CLONUS ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
COUGH ( 2 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 2 FDA reports)
DEAFNESS NEUROSENSORY ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 2 FDA reports)
GRANULOMA ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC NEOPLASM ( 2 FDA reports)
HEPATITIS B ( 2 FDA reports)
HERPES SIMPLEX ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
IMMUNOGLOBULINS ABNORMAL ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
JC VIRUS INFECTION ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LIFE SUPPORT ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MICROTIA ( 2 FDA reports)
MILLER FISHER SYNDROME ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MYELITIS ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
NERVE COMPRESSION ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NOCARDIOSIS ( 2 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PERITONEAL INFECTION ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 2 FDA reports)
PNEUMONIA FUNGAL ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PULMONARY VASCULITIS ( 2 FDA reports)
RADIATION SKIN INJURY ( 2 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SKIN GRAFT ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SYSTEMIC SCLEROSIS ( 2 FDA reports)
TONIC CONVULSION ( 2 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VASODILATATION ( 2 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
ABDOMINAL WALL ABSCESS ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACQUIRED HAEMOPHILIA ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ADENOVIRAL HEPATITIS ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
AMERICAN TRYPANOSOMIASIS ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
APLASIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BENCE JONES PROTEINURIA ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILE OUTPUT ABNORMAL ( 1 FDA reports)
BILIARY DRAINAGE ( 1 FDA reports)
BILIARY TRACT INFECTION ( 1 FDA reports)
BLAST CELL CRISIS ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BONE MARROW TUMOUR CELL INFILTRATION ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHROMOSOMAL DELETION ( 1 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 1 FDA reports)
CHRONIC HEPATIC FAILURE ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CSF VIRUS IDENTIFIED ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 1 FDA reports)
DEBRIDEMENT ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISSEMINATED CYTOMEGALOVIRAL INFECTION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENDOSCOPY ABNORMAL ( 1 FDA reports)
ENDOTHELIAL DYSFUNCTION ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENGRAFT FAILURE ( 1 FDA reports)
ENGRAFTMENT SYNDROME ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIGEN POSITIVE ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FACTOR VIII DEFICIENCY ( 1 FDA reports)
FACTOR VIII INHIBITION ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOETAL GROWTH RESTRICTION ( 1 FDA reports)
FOETAL HEART RATE DECREASED ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
FUNGAL SEPSIS ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC BYPASS ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTRITIS ATROPHIC ( 1 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 1 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 1 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRAFT LOSS ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMARTHROSIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 1 FDA reports)
HUMAN POLYOMAVIRUS INFECTION ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOSIDERAEMIA ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNOBLASTIC LYMPHOMA ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INSULIN C-PEPTIDE DECREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
INTUSSUSCEPTION ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LACTOBACILLUS INFECTION ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKODYSTROPHY ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOWER EXTREMITY MASS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LUNG TRANSPLANT REJECTION ( 1 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MASS ( 1 FDA reports)
MASS EXCISION ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDIASTINUM NEOPLASM ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTASES TO CHEST WALL ( 1 FDA reports)
METASTASES TO PERITONEUM ( 1 FDA reports)
METASTATIC GASTRIC CANCER ( 1 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MOYAMOYA DISEASE ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHROBLASTOMA ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANCREATIC MASS ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PAPILLARY MUSCLE HAEMORRHAGE ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PLASMA CELLS INCREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PREMATURE MENOPAUSE ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
REMOVAL OF RENAL TRANSPLANT ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL ISCHAEMIA ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RENAL SURGERY ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
RETINITIS ( 1 FDA reports)
RHODOCOCCUS INFECTION ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCINTILLATING SCOTOMA ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SICCA SYNDROME ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SPINAL DEFORMITY ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
SYSTEMIC MYCOSIS ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONSILLAR NEOPLASM ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRACHEITIS ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRANSPLANT ABSCESS ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VENOOCCLUSIVE DISEASE ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VIRAL TEST POSITIVE ( 1 FDA reports)
VIRUS BODY FLUID IDENTIFIED ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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