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

PYREXIA ( 54 FDA reports)
GRAFT VERSUS HOST DISEASE ( 48 FDA reports)
BLOOD BILIRUBIN INCREASED ( 28 FDA reports)
RENAL FAILURE ACUTE ( 28 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 26 FDA reports)
MULTI-ORGAN FAILURE ( 24 FDA reports)
DIARRHOEA ( 22 FDA reports)
HAEMOGLOBIN DECREASED ( 20 FDA reports)
RASH ( 20 FDA reports)
HYPOTENSION ( 19 FDA reports)
APLASTIC ANAEMIA ( 18 FDA reports)
CHILLS ( 18 FDA reports)
RENAL IMPAIRMENT ( 18 FDA reports)
SEPSIS ( 18 FDA reports)
BLOOD CREATININE INCREASED ( 17 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 17 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 16 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 16 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 16 FDA reports)
INFECTION ( 15 FDA reports)
PLATELET COUNT DECREASED ( 15 FDA reports)
RESPIRATORY FAILURE ( 15 FDA reports)
THROMBOCYTOPENIA ( 15 FDA reports)
HEADACHE ( 14 FDA reports)
HYPERTENSION ( 14 FDA reports)
DRUG INTERACTION ( 13 FDA reports)
DYSPNOEA ( 13 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 13 FDA reports)
TRANSPLANT REJECTION ( 13 FDA reports)
BONE MARROW FAILURE ( 12 FDA reports)
HAEMOLYTIC ANAEMIA ( 12 FDA reports)
HYPERSENSITIVITY ( 12 FDA reports)
URTICARIA ( 12 FDA reports)
ANAEMIA ( 11 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 11 FDA reports)
DRUG INEFFECTIVE ( 11 FDA reports)
HEPATIC FAILURE ( 11 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 11 FDA reports)
RENAL FAILURE ( 11 FDA reports)
RESPIRATORY DISTRESS ( 11 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
GENERALISED OEDEMA ( 10 FDA reports)
MUCOSAL INFLAMMATION ( 10 FDA reports)
MULTIPLE DRUG OVERDOSE ( 10 FDA reports)
PLEURAL EFFUSION ( 10 FDA reports)
SERUM SICKNESS ( 10 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 10 FDA reports)
CARDIAC ARREST ( 9 FDA reports)
DISEASE PROGRESSION ( 9 FDA reports)
NAUSEA ( 9 FDA reports)
PNEUMONIA ( 9 FDA reports)
TACHYCARDIA ( 9 FDA reports)
THROMBOSIS ( 9 FDA reports)
VIRAL INFECTION ( 9 FDA reports)
ABDOMINAL PAIN ( 8 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 8 FDA reports)
COUGH ( 8 FDA reports)
DEATH ( 8 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 8 FDA reports)
HYPONATRAEMIA ( 8 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 8 FDA reports)
INFUSION RELATED REACTION ( 8 FDA reports)
INTESTINAL ISCHAEMIA ( 8 FDA reports)
OEDEMA PERIPHERAL ( 8 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 7 FDA reports)
CONVULSION ( 7 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 7 FDA reports)
DYSSTASIA ( 7 FDA reports)
ENCEPHALITIS ( 7 FDA reports)
EPISTAXIS ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
LOSS OF CONSCIOUSNESS ( 7 FDA reports)
PANCYTOPENIA ( 7 FDA reports)
SEPTIC SHOCK ( 7 FDA reports)
VOMITING ( 7 FDA reports)
WEIGHT DECREASED ( 7 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 6 FDA reports)
AGITATION ( 6 FDA reports)
BACTERAEMIA ( 6 FDA reports)
CEREBRAL ATROPHY ( 6 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 6 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 6 FDA reports)
DISEASE RECURRENCE ( 6 FDA reports)
DRUG LEVEL INCREASED ( 6 FDA reports)
FEBRILE NEUTROPENIA ( 6 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 6 FDA reports)
HEPATIC FIBROSIS ( 6 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 6 FDA reports)
HERPES SIMPLEX ( 6 FDA reports)
JAUNDICE ( 6 FDA reports)
NEUTROPENIA ( 6 FDA reports)
STEM CELL TRANSPLANT ( 6 FDA reports)
TREMOR ( 6 FDA reports)
ASCITES ( 5 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 5 FDA reports)
CANDIDIASIS ( 5 FDA reports)
CEREBRAL HAEMORRHAGE ( 5 FDA reports)
CEREBRAL INFARCTION ( 5 FDA reports)
CHEST X-RAY ABNORMAL ( 5 FDA reports)
CYTOLYTIC HEPATITIS ( 5 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 5 FDA reports)
DEEP VEIN THROMBOSIS ( 5 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 5 FDA reports)
ENGRAFT FAILURE ( 5 FDA reports)
ENGRAFTMENT SYNDROME ( 5 FDA reports)
GASTROINTESTINAL NECROSIS ( 5 FDA reports)
HAPTOGLOBIN DECREASED ( 5 FDA reports)
HYPOXIA ( 5 FDA reports)
IRRITABILITY ( 5 FDA reports)
LEUKOPENIA ( 5 FDA reports)
LUNG DISORDER ( 5 FDA reports)
LUNG INFILTRATION ( 5 FDA reports)
LYMPHADENOPATHY ( 5 FDA reports)
MENTAL STATUS CHANGES ( 5 FDA reports)
NEUROTOXICITY ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 5 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 5 FDA reports)
PROTEINURIA ( 5 FDA reports)
RESPIRATORY ARREST ( 5 FDA reports)
THERAPY NON-RESPONDER ( 5 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 5 FDA reports)
TRANSPLANT FAILURE ( 5 FDA reports)
ADENOVIRUS INFECTION ( 4 FDA reports)
APLASIA PURE RED CELL ( 4 FDA reports)
ASPERGILLOSIS ( 4 FDA reports)
BACTERIAL INFECTION ( 4 FDA reports)
BK VIRUS INFECTION ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
BONE MARROW DEPRESSION ( 4 FDA reports)
BRAIN OEDEMA ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 4 FDA reports)
CD8 LYMPHOCYTES INCREASED ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
DIALYSIS ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
ENTEROCOLITIS ( 4 FDA reports)
EPSTEIN-BARR VIRUS ANTIGEN POSITIVE ( 4 FDA reports)
FACIAL PALSY ( 4 FDA reports)
FLUID OVERLOAD ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
GASTROINTESTINAL DISORDER ( 4 FDA reports)
GRAFT COMPLICATION ( 4 FDA reports)
HAEMATEMESIS ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 4 FDA reports)
HEPATOSPLENOMEGALY ( 4 FDA reports)
HYPERBILIRUBINAEMIA ( 4 FDA reports)
HYPOMAGNESAEMIA ( 4 FDA reports)
LEUKAEMIA RECURRENT ( 4 FDA reports)
MYDRIASIS ( 4 FDA reports)
NEUROLOGICAL SYMPTOM ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
OSTEONECROSIS ( 4 FDA reports)
PHOTOPHOBIA ( 4 FDA reports)
PNEUMONITIS ( 4 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
TRANSAMINASES INCREASED ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
ABDOMINAL TENDERNESS ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BONE MARROW TRANSPLANT ( 3 FDA reports)
BRAIN ABSCESS ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
CYSTITIS HAEMORRHAGIC ( 3 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 3 FDA reports)
EMBOLISM ( 3 FDA reports)
ENTERITIS ( 3 FDA reports)
ENTEROCOCCAL INFECTION ( 3 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 3 FDA reports)
GINGIVAL HYPERPLASIA ( 3 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 3 FDA reports)
GRAFT LOSS ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HAEMODYNAMIC INSTABILITY ( 3 FDA reports)
HAEMOLYSIS ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
HYPERAESTHESIA ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
HYPOREFLEXIA ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
LIVER ABSCESS ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
NEPHROPATHY TOXIC ( 3 FDA reports)
OSTEOMYELITIS ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PHLEBITIS ( 3 FDA reports)
POST TRANSPLANT DISTAL LIMB SYNDROME ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
PULSE ABSENT ( 3 FDA reports)
RASH MACULO-PAPULAR ( 3 FDA reports)
RENAL CYST ( 3 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SPINAL DEFORMITY ( 3 FDA reports)
TACHYPNOEA ( 3 FDA reports)
THROAT IRRITATION ( 3 FDA reports)
TOXIC ENCEPHALOPATHY ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
VENOOCCLUSIVE DISEASE ( 3 FDA reports)
VIITH NERVE PARALYSIS ( 3 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
ZYGOMYCOSIS ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
AMAUROSIS ( 2 FDA reports)
ANAL HAEMORRHAGE ( 2 FDA reports)
ANEURYSM ( 2 FDA reports)
ANURIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BACTERIAL SEPSIS ( 2 FDA reports)
BASAL CELL CARCINOMA ( 2 FDA reports)
BLEEDING TIME PROLONGED ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
CAPILLARY LEAK SYNDROME ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CARDIOTOXICITY ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
COMA ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CSF LYMPHOCYTE COUNT ABNORMAL ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DERMAL CYST ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ENTEROBACTER INFECTION ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
EXTRAVASATION ( 2 FDA reports)
EYE INFECTION VIRAL ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
GINGIVECTOMY ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HAEMOSIDEROSIS ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERKERATOSIS ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
INTESTINAL RESECTION ( 2 FDA reports)
INTUSSUSCEPTION ( 2 FDA reports)
KRABBE'S DISEASE ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LIFE SUPPORT ( 2 FDA reports)
LIVER TRANSPLANT ( 2 FDA reports)
LUNG ADENOCARCINOMA ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MUCOUS STOOLS ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NEPHRECTOMY ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
NERVE INJURY ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 2 FDA reports)
NOSOCOMIAL INFECTION ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 2 FDA reports)
OESOPHAGEAL CARCINOMA RECURRENT ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PANCREATIC DISORDER ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PARVOVIRUS INFECTION ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 2 FDA reports)
PNEUMONIA ASPERGILLUS ( 2 FDA reports)
PNEUMONIA FUNGAL ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PROCTALGIA ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 2 FDA reports)
REFRACTORINESS TO PLATELET TRANSFUSION ( 2 FDA reports)
RENAL HAEMORRHAGE ( 2 FDA reports)
RENAL INFARCT ( 2 FDA reports)
RENAL TUBULAR ACIDOSIS ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 2 FDA reports)
RHONCHI ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SIMPLE PARTIAL SEIZURES ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SKIN LESION EXCISION ( 2 FDA reports)
SKIN NODULE ( 2 FDA reports)
SKIN PAPILLOMA ( 2 FDA reports)
SPLEEN DISORDER ( 2 FDA reports)
SPLENECTOMY ( 2 FDA reports)
SPLENIC ABSCESS ( 2 FDA reports)
SPLENIC NEOPLASM MALIGNANCY UNSPECIFIED ( 2 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
SYSTEMIC MYCOSIS ( 2 FDA reports)
TONSILLITIS ( 2 FDA reports)
TOXOPLASMOSIS ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
URETERIC OBSTRUCTION ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABDOMINAL WALL ANOMALY ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ADENOVIRAL HEPATITIS ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APOPTOSIS ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BASEDOW'S DISEASE ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CARDIAC PSEUDOANEURYSM ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CAT SCRATCH DISEASE ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM NECROSIS ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLD AGGLUTININS POSITIVE ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COMPLEMENT FACTOR DECREASED ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
COOMBS NEGATIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CYSTITIS KLEBSIELLA ( 1 FDA reports)
CYTOKINE STORM ( 1 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 1 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 1 FDA reports)
DEBRIDEMENT ( 1 FDA reports)
DELAYED ENGRAFTMENT ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISSEMINATED CYTOMEGALOVIRAL INFECTION ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DUODENITIS HAEMORRHAGIC ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
ENCEPHALITIS POST MEASLES ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 1 FDA reports)
EVAN'S SYNDROME ( 1 FDA reports)
EVANS SYNDROME ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FUNGAL ABSCESS CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
FUNGAL SEPSIS ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROENTERITIS CRYPTOSPORIDIAL ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRAFT THROMBOSIS ( 1 FDA reports)
GRAM STAIN NEGATIVE ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEMISENSORY NEGLECT ( 1 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE CELLULITIS ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INTRACRANIAL HAEMATOMA ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LUMBAR PUNCTURE ABNORMAL ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MASS ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MEDIASTINAL HAEMATOMA ( 1 FDA reports)
MEDIASTINITIS ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MILLER FISHER SYNDROME ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MUCOSAL INFECTION ( 1 FDA reports)
MYCOPLASMA TEST POSITIVE ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOCARDITIS BACTERIAL ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECROTISING GASTRITIS ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE IV ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOLYSIS ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PLASMAPHERESIS ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONIA HERPES VIRAL ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POLYSEROSITIS ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 1 FDA reports)
PSEUDALLESCHERIA INFECTION ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
RADICULOPATHY ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL AGGLUTINATION ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
REMOVAL OF RENAL TRANSPLANT ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RESPIRATORY GAS EXCHANGE DISORDER ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETICULOCYTOSIS ( 1 FDA reports)
RETINAL VASCULITIS ( 1 FDA reports)
RETROPERITONEAL NEOPLASM ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
ROTAVIRUS INFECTION ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
THYROXINE FREE INCREASED ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VIRAL LOAD INCREASED ( 1 FDA reports)
VIRAL PHARYNGITIS ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VITH NERVE PARALYSIS ( 1 FDA reports)
VITILIGO ( 1 FDA reports)
VON WILLEBRAND'S DISEASE ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)

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