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

ACUTE GRAFT VERSUS HOST DISEASE ( 114 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 106 FDA reports)
PYREXIA ( 95 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 80 FDA reports)
GRAFT VERSUS HOST DISEASE ( 69 FDA reports)
SEPSIS ( 68 FDA reports)
DRUG INEFFECTIVE ( 66 FDA reports)
DEATH ( 60 FDA reports)
MULTI-ORGAN FAILURE ( 51 FDA reports)
PNEUMONIA ( 49 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 45 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 45 FDA reports)
HYPERTENSION ( 42 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 40 FDA reports)
TRANSPLANT REJECTION ( 40 FDA reports)
BLOOD BILIRUBIN INCREASED ( 39 FDA reports)
MUCOSAL INFLAMMATION ( 39 FDA reports)
OEDEMA ( 33 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 31 FDA reports)
RENAL IMPAIRMENT ( 30 FDA reports)
RENAL FAILURE ( 29 FDA reports)
RESPIRATORY FAILURE ( 29 FDA reports)
SEPTIC SHOCK ( 28 FDA reports)
APLASIA ( 27 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 27 FDA reports)
INFECTION ( 27 FDA reports)
NEPHROPATHY TOXIC ( 27 FDA reports)
TRANSAMINASES INCREASED ( 27 FDA reports)
ADENOVIRUS INFECTION ( 26 FDA reports)
CYSTITIS HAEMORRHAGIC ( 26 FDA reports)
DIARRHOEA ( 26 FDA reports)
DYSPNOEA ( 26 FDA reports)
NAUSEA ( 26 FDA reports)
TRANSPLANT FAILURE ( 26 FDA reports)
VENOOCCLUSIVE DISEASE ( 26 FDA reports)
THROMBOCYTOPENIA ( 25 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 24 FDA reports)
PANCYTOPENIA ( 23 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 23 FDA reports)
PLEURAL EFFUSION ( 22 FDA reports)
VOMITING ( 22 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 21 FDA reports)
CEREBRAL HAEMORRHAGE ( 20 FDA reports)
NEUROTOXICITY ( 20 FDA reports)
BACTERIAL SEPSIS ( 19 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 19 FDA reports)
DIABETES MELLITUS ( 19 FDA reports)
HERPES ZOSTER ( 19 FDA reports)
STATUS EPILEPTICUS ( 19 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 18 FDA reports)
FEBRILE NEUTROPENIA ( 18 FDA reports)
STAPHYLOCOCCAL INFECTION ( 18 FDA reports)
ABDOMINAL PAIN ( 17 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 17 FDA reports)
ASPERGILLOSIS ( 17 FDA reports)
BK VIRUS INFECTION ( 16 FDA reports)
HEADACHE ( 16 FDA reports)
LUNG INFILTRATION ( 16 FDA reports)
MYELODYSPLASTIC SYNDROME ( 16 FDA reports)
RENAL FAILURE ACUTE ( 16 FDA reports)
ASCITES ( 15 FDA reports)
BLOOD CREATININE INCREASED ( 15 FDA reports)
HEPATOTOXICITY ( 15 FDA reports)
PNEUMONITIS ( 15 FDA reports)
SKIN TOXICITY ( 15 FDA reports)
STOMATITIS ( 15 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 14 FDA reports)
BRAIN OEDEMA ( 14 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 14 FDA reports)
JAUNDICE ( 14 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 13 FDA reports)
ANAEMIA ( 13 FDA reports)
CANDIDIASIS ( 13 FDA reports)
HYPOTENSION ( 13 FDA reports)
NEUTROPENIA ( 13 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 13 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 13 FDA reports)
CARDIO-RESPIRATORY ARREST ( 12 FDA reports)
HYPERGLYCAEMIA ( 12 FDA reports)
LEUKOPENIA ( 12 FDA reports)
LIVER DISORDER ( 12 FDA reports)
LYMPHADENOPATHY ( 12 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 12 FDA reports)
PERICARDIAL EFFUSION ( 12 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 11 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
CYSTITIS VIRAL ( 11 FDA reports)
ESCHERICHIA SEPSIS ( 11 FDA reports)
ORGANISING PNEUMONIA ( 11 FDA reports)
OSTEONECROSIS ( 11 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 11 FDA reports)
PULMONARY OEDEMA ( 11 FDA reports)
STEM CELL TRANSPLANT ( 11 FDA reports)
BACTERIAL INFECTION ( 10 FDA reports)
BRONCHIECTASIS ( 10 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 10 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 10 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 10 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 10 FDA reports)
PANCREATITIS ACUTE ( 10 FDA reports)
PLATELET COUNT DECREASED ( 10 FDA reports)
RENAL TUBULAR NECROSIS ( 10 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
BURKHOLDERIA CEPACIA COMPLEX SEPSIS ( 9 FDA reports)
CANDIDA SEPSIS ( 9 FDA reports)
CHOLESTASIS ( 9 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 9 FDA reports)
CONDITION AGGRAVATED ( 9 FDA reports)
CONVULSION ( 9 FDA reports)
DECREASED APPETITE ( 9 FDA reports)
DISEASE PROGRESSION ( 9 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 9 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 9 FDA reports)
NO THERAPEUTIC RESPONSE ( 9 FDA reports)
OLIGURIA ( 9 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 9 FDA reports)
RASH ( 9 FDA reports)
RENAL CELL CARCINOMA ( 9 FDA reports)
RESPIRATORY DISORDER ( 9 FDA reports)
URINARY TRACT INFECTION ( 9 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 9 FDA reports)
VIRAL INFECTION ( 9 FDA reports)
ADRENAL INSUFFICIENCY ( 8 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 8 FDA reports)
CARDIAC FAILURE ( 8 FDA reports)
DRUG TOXICITY ( 8 FDA reports)
FUNGAL INFECTION ( 8 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 8 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 8 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 8 FDA reports)
HYPERCALCAEMIA ( 8 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 8 FDA reports)
ILEUS PARALYTIC ( 8 FDA reports)
INFLAMMATION ( 8 FDA reports)
PAIN IN EXTREMITY ( 8 FDA reports)
PNEUMONIA BACTERIAL ( 8 FDA reports)
PRECURSOR T-LYMPHOBLASTIC LYMPHOMA/LEUKAEMIA ( 8 FDA reports)
PULMONARY HAEMORRHAGE ( 8 FDA reports)
RENAL DISORDER ( 8 FDA reports)
RESPIRATORY DISTRESS ( 8 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 8 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 8 FDA reports)
ZYGOMYCOSIS ( 8 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 7 FDA reports)
BONE MARROW FAILURE ( 7 FDA reports)
CARDIAC ARREST ( 7 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 7 FDA reports)
DRUG RESISTANCE ( 7 FDA reports)
FUSARIUM INFECTION ( 7 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 7 FDA reports)
HAEMODIALYSIS ( 7 FDA reports)
KLEBSIELLA INFECTION ( 7 FDA reports)
LUNG NEOPLASM ( 7 FDA reports)
LYMPHOPENIA ( 7 FDA reports)
ALTERNARIA INFECTION ( 6 FDA reports)
AORTIC DISSECTION ( 6 FDA reports)
CELLULITIS ( 6 FDA reports)
CEREBROVASCULAR ACCIDENT ( 6 FDA reports)
CEREBROVASCULAR SPASM ( 6 FDA reports)
CHEST X-RAY ABNORMAL ( 6 FDA reports)
CHOLECYSTITIS ( 6 FDA reports)
COLITIS ( 6 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 6 FDA reports)
CONFUSIONAL STATE ( 6 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
ENGRAFT FAILURE ( 6 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
HYPONATRAEMIA ( 6 FDA reports)
HYPOPROTEINAEMIA ( 6 FDA reports)
INFLUENZA ( 6 FDA reports)
MELAENA ( 6 FDA reports)
MICROANGIOPATHY ( 6 FDA reports)
MUCORMYCOSIS ( 6 FDA reports)
ORAL HERPES ( 6 FDA reports)
PAPILLOMA VIRAL INFECTION ( 6 FDA reports)
PELIOSIS HEPATIS ( 6 FDA reports)
PULMONARY TUBERCULOSIS ( 6 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 6 FDA reports)
SKIN EROSION ( 6 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 6 FDA reports)
VANISHING BILE DUCT SYNDROME ( 6 FDA reports)
ACUTE RESPIRATORY FAILURE ( 5 FDA reports)
ADENOVIRAL HEPATITIS ( 5 FDA reports)
BACILLUS INFECTION ( 5 FDA reports)
BICYTOPENIA ( 5 FDA reports)
BLOOD MAGNESIUM DECREASED ( 5 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
CHILLS ( 5 FDA reports)
COMA ( 5 FDA reports)
COUGH ( 5 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE IV ( 5 FDA reports)
DISEASE RECURRENCE ( 5 FDA reports)
DISSEMINATED TUBERCULOSIS ( 5 FDA reports)
ENCEPHALITIS ( 5 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 5 FDA reports)
FEELING COLD ( 5 FDA reports)
FLUID OVERLOAD ( 5 FDA reports)
GRAFT LOSS ( 5 FDA reports)
GRAFT VERSUS HOST DISEASE IN LIVER ( 5 FDA reports)
HAEMATURIA ( 5 FDA reports)
HAEMOLYTIC ANAEMIA ( 5 FDA reports)
HEPATIC ENZYME INCREASED ( 5 FDA reports)
HEPATIC FAILURE ( 5 FDA reports)
HEPATIC LESION ( 5 FDA reports)
HERPES SIMPLEX ( 5 FDA reports)
HYPERLIPIDAEMIA ( 5 FDA reports)
HYPOAESTHESIA FACIAL ( 5 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 5 FDA reports)
IMPAIRED HEALING ( 5 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 5 FDA reports)
KIDNEY FIBROSIS ( 5 FDA reports)
LETHARGY ( 5 FDA reports)
LEUKAEMIA RECURRENT ( 5 FDA reports)
LIVER INJURY ( 5 FDA reports)
LIVER TRANSPLANT ( 5 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 5 FDA reports)
MALAISE ( 5 FDA reports)
METABOLIC DISORDER ( 5 FDA reports)
MYCOBACTERIUM ABSCESSUS INFECTION ( 5 FDA reports)
NEOPLASM MALIGNANT ( 5 FDA reports)
NEUROPATHY PERIPHERAL ( 5 FDA reports)
NODULE ( 5 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
PARAESTHESIA ( 5 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 5 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 5 FDA reports)
SERUM SICKNESS ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
SPLENOMEGALY ( 5 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 5 FDA reports)
TOXIC ENCEPHALOPATHY ( 5 FDA reports)
TOXOPLASMOSIS ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
AGRANULOCYTOSIS ( 4 FDA reports)
APALLIC SYNDROME ( 4 FDA reports)
APHASIA ( 4 FDA reports)
APLASTIC ANAEMIA ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 4 FDA reports)
CRYPTOCOCCOSIS ( 4 FDA reports)
CYTOLYTIC HEPATITIS ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
ENCEPHALOPATHY ( 4 FDA reports)
EVANS SYNDROME ( 4 FDA reports)
EYE INFECTION FUNGAL ( 4 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
GRAND MAL CONVULSION ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 4 FDA reports)
HEPATITIS B ( 4 FDA reports)
HERPES VIRUS INFECTION ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
IRRITABILITY ( 4 FDA reports)
ISCHAEMIC STROKE ( 4 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 4 FDA reports)
LEUKOENCEPHALOPATHY ( 4 FDA reports)
LYMPHOCELE ( 4 FDA reports)
MALACOPLAKIA GASTROINTESTINAL ( 4 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 4 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 4 FDA reports)
MENINGOENCEPHALITIS HERPETIC ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
NECROSIS ( 4 FDA reports)
NEPHRITIS ( 4 FDA reports)
NEPHROTIC SYNDROME ( 4 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 4 FDA reports)
NEUTROPHIL COUNT DECREASED ( 4 FDA reports)
PANIC ATTACK ( 4 FDA reports)
PERITONITIS BACTERIAL ( 4 FDA reports)
PNEUMOTHORAX ( 4 FDA reports)
POLYSEROSITIS ( 4 FDA reports)
POST PROCEDURAL COMPLICATION ( 4 FDA reports)
PROTEINURIA ( 4 FDA reports)
PSEUDOMONAL SEPSIS ( 4 FDA reports)
PSEUDOMONAS INFECTION ( 4 FDA reports)
RECURRENT CANCER ( 4 FDA reports)
SKIN NODULE ( 4 FDA reports)
SUBDURAL HAEMORRHAGE ( 4 FDA reports)
SWELLING ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 4 FDA reports)
TACHYARRHYTHMIA ( 4 FDA reports)
URETERAL NECROSIS ( 4 FDA reports)
URINE OUTPUT DECREASED ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
ANGIOCENTRIC LYMPHOMA ( 3 FDA reports)
ANURIA ( 3 FDA reports)
APLASIA PURE RED CELL ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BACTERAEMIA ( 3 FDA reports)
BASAL CELL CARCINOMA ( 3 FDA reports)
BODY HEIGHT BELOW NORMAL ( 3 FDA reports)
BRAIN ABSCESS ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CEREBRAL FUNGAL INFECTION ( 3 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA RECURRENT ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
ENDOCARDITIS ( 3 FDA reports)
ENGRAFTMENT SYNDROME ( 3 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
ESCHERICHIA INFECTION ( 3 FDA reports)
EYE MOVEMENT DISORDER ( 3 FDA reports)
FIBROADENOMA OF BREAST ( 3 FDA reports)
FUNGAL SEPSIS ( 3 FDA reports)
GAMMOPATHY ( 3 FDA reports)
GASTRIC CANCER ( 3 FDA reports)
GASTROENTERITIS VIRAL ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GRANULOMA ( 3 FDA reports)
GROWTH HORMONE DEFICIENCY ( 3 FDA reports)
HAEMODYNAMIC INSTABILITY ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HEMIPLEGIA ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HEPATITIS E ( 3 FDA reports)
HEPATITIS FULMINANT ( 3 FDA reports)
HYPERBILIRUBINAEMIA ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
HYPOPHAGIA ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
KAPOSI'S SARCOMA ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
LYMPHOMA ( 3 FDA reports)
MECHANICAL VENTILATION ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MENINGITIS ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
OPTIC NEURITIS ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
OSTEOPENIA ( 3 FDA reports)
PAIN ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PLEURITIC PAIN ( 3 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 3 FDA reports)
PULMONARY TOXICITY ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 3 FDA reports)
RENAL CYST ( 3 FDA reports)
RETINITIS ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
ROTAVIRUS INFECTION ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SINUSITIS ( 3 FDA reports)
SINUSITIS FUNGAL ( 3 FDA reports)
SKIN HAEMORRHAGE ( 3 FDA reports)
SOFT TISSUE INFECTION ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA ( 3 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 3 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 3 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
SYSTEMIC CANDIDA ( 3 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 3 FDA reports)
SYSTEMIC MYCOSIS ( 3 FDA reports)
UROSEPSIS ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 3 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ACQUIRED HAEMOPHILIA ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
AMYLOIDOSIS ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANTEROGRADE AMNESIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 2 FDA reports)
AUTOIMMUNE PANCYTOPENIA ( 2 FDA reports)
B-CELL LYMPHOMA ( 2 FDA reports)
B-CELL LYMPHOMA STAGE IV ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRAIN DEATH ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CATHETER SITE INFECTION ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CEREBELLAR ATROPHY ( 2 FDA reports)
CEREBRAL ASPERGILLOSIS ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CERVIX CARCINOMA ( 2 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE IN SKIN ( 2 FDA reports)
COLLATERAL CIRCULATION ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
CSF MONOCYTE COUNT POSITIVE ( 2 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 2 FDA reports)
DECEREBRATION ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DEPRESSIVE SYMPTOM ( 2 FDA reports)
DEVELOPMENTAL DELAY ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DIABETES INSIPIDUS ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE II ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
EAR INFECTION BACTERIAL ( 2 FDA reports)
ENCEPHALITIS HERPES ( 2 FDA reports)
ENTERITIS ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
ENTEROCOCCAL SEPSIS ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 2 FDA reports)
ESCHERICHIA BACTERAEMIA ( 2 FDA reports)
FACTOR VIII DEFICIENCY ( 2 FDA reports)
FACTOR VIII INHIBITION ( 2 FDA reports)
FALL ( 2 FDA reports)
FAMILIAL MEDITERRANEAN FEVER ( 2 FDA reports)
FASCIITIS ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 2 FDA reports)
FOOD ALLERGY ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GASTRITIS BACTERIAL ( 2 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL NECROSIS ( 2 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 2 FDA reports)
GASTROINTESTINAL OEDEMA ( 2 FDA reports)
GINGIVAL HYPERPLASIA ( 2 FDA reports)
GLIOSIS ( 2 FDA reports)
GLOMERULOSCLEROSIS ( 2 FDA reports)
GRAFT DYSFUNCTION ( 2 FDA reports)
GRAFT INFECTION ( 2 FDA reports)
HAEMARTHROSIS ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMATOTOXICITY ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HALLUCINATION, AUDITORY ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC ENZYME ABNORMAL ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HEPATOBILIARY DISEASE ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HERPES SEPSIS ( 2 FDA reports)
HIRSUTISM ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPERAEMIA ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
IDIOPATHIC PNEUMONIA SYNDROME ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 2 FDA reports)
INJURY ( 2 FDA reports)
INTESTINAL HAEMORRHAGE ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
JUGULAR VEIN THROMBOSIS ( 2 FDA reports)
LICHENOID KERATOSIS ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
LIVER ABSCESS ( 2 FDA reports)
LIVER TRANSPLANT REJECTION ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LYMPHADENITIS ( 2 FDA reports)
MANTLE CELL LYMPHOMA ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
MENINGITIS HERPES ( 2 FDA reports)
MENINGITIS TUBERCULOUS ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYCOBACTERIAL INFECTION ( 2 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 2 FDA reports)
MYCOTIC ANEURYSM ( 2 FDA reports)
MYELITIS ( 2 FDA reports)
MYELOMA RECURRENCE ( 2 FDA reports)
MYOPATHY TOXIC ( 2 FDA reports)
NASAL CAVITY CANCER ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEUROBLASTOMA ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
NOSOCOMIAL INFECTION ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
PANCREAS TRANSPLANT REJECTION ( 2 FDA reports)
PANCREATIC ABSCESS ( 2 FDA reports)
PAPILLOEDEMA ( 2 FDA reports)
PARVOVIRUS INFECTION ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERITONEAL HAEMORRHAGE ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHARYNGEAL INFLAMMATION ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PLATELET DISORDER ( 2 FDA reports)
PNEUMATOSIS INTESTINALIS ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PNEUMONIA FUNGAL ( 2 FDA reports)
POLYCYTHAEMIA ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
PORPHYRIA NON-ACUTE ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
POST TRANSPLANT DISTAL LIMB SYNDROME ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
PYELONEPHRITIS ACUTE ( 2 FDA reports)
RALES ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
REFRACTORINESS TO PLATELET TRANSFUSION ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RENAL HYPERTROPHY ( 2 FDA reports)
RENAL INJURY ( 2 FDA reports)
RENAL PAPILLARY NECROSIS ( 2 FDA reports)
RENAL TUBULAR ATROPHY ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS BRONCHIOLITIS ( 2 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SCLERODERMA ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SICCA SYNDROME ( 2 FDA reports)
SINUSITIS ASPERGILLUS ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SKIN PAPILLOMA ( 2 FDA reports)
SPINAL DEFORMITY ( 2 FDA reports)
STENOTROPHOMONAS INFECTION ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 2 FDA reports)
SURGICAL PROCEDURE REPEATED ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
TIBIA FRACTURE ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VARICELLA VIRUS TEST POSITIVE ( 2 FDA reports)
VASCULAR PSEUDOANEURYSM ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
WEANING FAILURE ( 2 FDA reports)
WHITE BLOOD CELL DISORDER ( 2 FDA reports)
ABDOMINAL ABSCESS ( 1 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACINETOBACTER TEST POSITIVE ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ADENOVIRUS TEST POSITIVE ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
AMINO ACID METABOLISM DISORDER ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY POSITIVE ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC ANEURYSM RUPTURE ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
AUTOIMMUNE PANCREATITIS ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
B-CELL LYMPHOMA STAGE II ( 1 FDA reports)
BACTERIAL DISEASE CARRIER ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BACTERIURIA ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILIARY ISCHAEMIA ( 1 FDA reports)
BIOPSY LUNG ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD GLUCAGON INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 1 FDA reports)
BONE MARROW OEDEMA ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BONE MARROW TRANSPLANT REJECTION ( 1 FDA reports)
BONE SARCOMA ( 1 FDA reports)
BONE TUBERCULOSIS ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BUTTERFLY RASH ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CATHETER CULTURE POSITIVE ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CELL MARKER INCREASED ( 1 FDA reports)
CELL-MEDIATED IMMUNE DEFICIENCY ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFLAMMATION ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHIMERISM ( 1 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CITROBACTER SEPSIS ( 1 FDA reports)
CLONUS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONJUNCTIVAL PALLOR ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CRYING ( 1 FDA reports)
CRYPTOSPORIDIOSIS INFECTION ( 1 FDA reports)
CSF LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CYSTITIS KLEBSIELLA ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 1 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 1 FDA reports)
DEBRIDEMENT ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DEVICE OCCLUSION ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE I ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DUCHENNE MUSCULAR DYSTROPHY ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ABNORMAL ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ENTEROVIRUS INFECTION ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EYE INFECTION BACTERIAL ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECAL VOLUME DECREASED ( 1 FDA reports)
FEBRILE INFECTION ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FUNGAL ENDOCARDITIS ( 1 FDA reports)
GALLBLADDER ABSCESS ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROENTERITIS EOSINOPHILIC ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GINGIVAL HYPERTROPHY ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE IN LUNG ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATIC VEIN OCCLUSION ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS C VIRUS TEST ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HERPES OPHTHALMIC ( 1 FDA reports)
HISTIOCYTIC NECROTISING LYMPHADENITIS ( 1 FDA reports)
HISTIOCYTOSIS ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY ( 1 FDA reports)
HUMAN POLYOMAVIRUS INFECTION ( 1 FDA reports)
HYDROPHOBIA ( 1 FDA reports)
HYPERALBUMINAEMIA ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 1 FDA reports)
HYPERPROTEINAEMIA ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOGONADISM ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
ILEAL PERFORATION ( 1 FDA reports)
ILEAL STENOSIS ( 1 FDA reports)
IMMUNOGLOBULINS DECREASED ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
JOINT SURGERY ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LASER THERAPY ( 1 FDA reports)
LEUKAEMIC INFILTRATION BRAIN ( 1 FDA reports)
LEUKODYSTROPHY ( 1 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOWER EXTREMITY MASS ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG TRANSPLANT REJECTION ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPHANGIOPATHY ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
MACULE ( 1 FDA reports)
MECHANICAL VENTILATION COMPLICATION ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MEGACOLON ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
MICROSPORIDIA INFECTION ( 1 FDA reports)
MINERAL METABOLISM DISORDER ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOTOR DEVELOPMENTAL DELAY ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUCOUS STOOLS ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NATURAL KILLER T CELL COUNT INCREASED ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
OBSTRUCTIVE UROPATHY ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAPILLOMA ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PARESIS CRANIAL NERVE ( 1 FDA reports)
PARONYCHIA ( 1 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PENILE ABSCESS ( 1 FDA reports)
PERICARDITIS FUNGAL ( 1 FDA reports)
PERITONEAL INFECTION ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
PLEOCYTOSIS ( 1 FDA reports)
PNEUMOMEDIASTINUM ( 1 FDA reports)
PNEUMONIA HERPES VIRAL ( 1 FDA reports)
PNEUMONIA PARAINFLUENZAE VIRAL ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
PORTAL VEIN FLOW DECREASED ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POST PROCEDURAL SEPSIS ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDALLESCHERIA INFECTION ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULMONARY SEPSIS ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PYELOCALIECTASIS ( 1 FDA reports)
PYURIA ( 1 FDA reports)
RADIOTHERAPY TO SKIN ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFRACTORY ANAEMIA ( 1 FDA reports)
REFRACTORY ANAEMIA WITH AN EXCESS OF BLASTS ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL GRAFT LOSS ( 1 FDA reports)
RENAL ISCHAEMIA ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESPIROVIRUS TEST POSITIVE ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEPSIS SYNDROME ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN LESION EXCISION ( 1 FDA reports)
SKIN MASS ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPLENIC HAEMORRHAGE ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 1 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SURFACTANT PROTEIN INCREASED ( 1 FDA reports)
SURGERY ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TRANSFUSION ( 1 FDA reports)
TRANSFUSION ASSOCIATED GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY RETENTION POSTOPERATIVE ( 1 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 1 FDA reports)
URINE OSMOLARITY DECREASED ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VESICOURETERAL REFLUX SURGERY ( 1 FDA reports)
VESICOURETERIC REFLUX ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use