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

CYTOMEGALOVIRUS INFECTION ( 177 FDA reports)
PYREXIA ( 135 FDA reports)
NEUTROPENIA ( 127 FDA reports)
SEPSIS ( 104 FDA reports)
MULTI-ORGAN FAILURE ( 92 FDA reports)
FEBRILE NEUTROPENIA ( 91 FDA reports)
THROMBOCYTOPENIA ( 86 FDA reports)
PNEUMONIA ( 77 FDA reports)
PANCYTOPENIA ( 74 FDA reports)
SUICIDAL IDEATION ( 67 FDA reports)
HEADACHE ( 66 FDA reports)
GRAFT VERSUS HOST DISEASE ( 60 FDA reports)
DIARRHOEA ( 58 FDA reports)
NAUSEA ( 57 FDA reports)
ANAEMIA ( 54 FDA reports)
RENAL FAILURE ( 54 FDA reports)
DYSPNOEA ( 48 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 47 FDA reports)
INFECTION ( 46 FDA reports)
HYPERTHYROIDISM ( 43 FDA reports)
RESPIRATORY FAILURE ( 43 FDA reports)
VOMITING ( 43 FDA reports)
ADENOVIRUS INFECTION ( 42 FDA reports)
FUNGAL INFECTION ( 39 FDA reports)
RENAL FAILURE ACUTE ( 39 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 37 FDA reports)
FATIGUE ( 37 FDA reports)
RASH ( 37 FDA reports)
URINARY TRACT INFECTION ( 36 FDA reports)
SEPTIC SHOCK ( 35 FDA reports)
BONE MARROW FAILURE ( 33 FDA reports)
CERVICAL DYSPLASIA ( 32 FDA reports)
HERPES SIMPLEX ( 31 FDA reports)
LYMPHOPENIA ( 31 FDA reports)
HYSTERECTOMY ( 30 FDA reports)
NEUTROPHIL COUNT DECREASED ( 30 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 29 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 29 FDA reports)
TRANSPLANT REJECTION ( 29 FDA reports)
DRUG INEFFECTIVE ( 28 FDA reports)
HYPOTENSION ( 28 FDA reports)
HYPOTHYROIDISM ( 28 FDA reports)
INFUSION RELATED REACTION ( 28 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 27 FDA reports)
DEHYDRATION ( 27 FDA reports)
HEPATIC FAILURE ( 27 FDA reports)
CONVULSION ( 26 FDA reports)
DEATH ( 26 FDA reports)
ENCEPHALITIS ( 26 FDA reports)
HEPATITIS ( 26 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 26 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 25 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 25 FDA reports)
PLEURISY ( 25 FDA reports)
BREAST CANCER ( 24 FDA reports)
LEUKOPENIA ( 24 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 24 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 23 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 23 FDA reports)
HYPERTENSION ( 23 FDA reports)
OEDEMA PERIPHERAL ( 23 FDA reports)
PNEUMONITIS ( 23 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 23 FDA reports)
ASTHENIA ( 22 FDA reports)
BK VIRUS INFECTION ( 22 FDA reports)
LUNG INFECTION ( 22 FDA reports)
PULMONARY TUBERCULOSIS ( 22 FDA reports)
TUBERCULOSIS ( 22 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 21 FDA reports)
BACTERIAL INFECTION ( 21 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 21 FDA reports)
GASTROINTESTINAL DISORDER ( 21 FDA reports)
HAEMOLYTIC ANAEMIA ( 21 FDA reports)
LUNG INFILTRATION ( 21 FDA reports)
RESPIRATORY DISTRESS ( 21 FDA reports)
TACHYCARDIA ( 21 FDA reports)
CONFUSIONAL STATE ( 20 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 20 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 20 FDA reports)
WEIGHT DECREASED ( 20 FDA reports)
DIZZINESS ( 19 FDA reports)
RENAL IMPAIRMENT ( 19 FDA reports)
TRANSAMINASES INCREASED ( 19 FDA reports)
ABDOMINAL PAIN ( 18 FDA reports)
ABORTION SPONTANEOUS ( 18 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 18 FDA reports)
HERPES ZOSTER ( 18 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 18 FDA reports)
MUCOSAL INFLAMMATION ( 18 FDA reports)
NEPHROPATHY TOXIC ( 18 FDA reports)
PNEUMONIA BACTERIAL ( 18 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 17 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 17 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 17 FDA reports)
INFLUENZA LIKE ILLNESS ( 17 FDA reports)
MYELODYSPLASTIC SYNDROME ( 17 FDA reports)
OEDEMA ( 17 FDA reports)
VENOOCCLUSIVE DISEASE ( 17 FDA reports)
BLOOD CREATININE INCREASED ( 16 FDA reports)
CYSTITIS VIRAL ( 16 FDA reports)
CYTOKINE RELEASE SYNDROME ( 16 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 16 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 16 FDA reports)
URINE OUTPUT DECREASED ( 16 FDA reports)
ASPERGILLOSIS ( 15 FDA reports)
COAGULOPATHY ( 15 FDA reports)
DISSEMINATED CYTOMEGALOVIRAL INFECTION ( 15 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 15 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 15 FDA reports)
NEUROPATHY PERIPHERAL ( 15 FDA reports)
PALPITATIONS ( 15 FDA reports)
PSEUDOMONAL SEPSIS ( 15 FDA reports)
QUADRIPARESIS ( 15 FDA reports)
RESPIRATORY RATE INCREASED ( 15 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 14 FDA reports)
DEEP VEIN THROMBOSIS ( 14 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 14 FDA reports)
GASTRITIS ( 14 FDA reports)
GASTROENTERITIS ( 14 FDA reports)
NEOPLASM MALIGNANT ( 14 FDA reports)
OXYGEN SATURATION DECREASED ( 14 FDA reports)
PLEURAL EFFUSION ( 14 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 13 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 13 FDA reports)
AUTOIMMUNE THYROIDITIS ( 13 FDA reports)
HYPERBILIRUBINAEMIA ( 13 FDA reports)
INTERSTITIAL LUNG DISEASE ( 13 FDA reports)
VERTIGO ( 13 FDA reports)
VULVAL CANCER STAGE 0 ( 13 FDA reports)
VULVAR DYSPLASIA ( 13 FDA reports)
BASEDOW'S DISEASE ( 12 FDA reports)
BRADYCARDIA ( 12 FDA reports)
DISEASE PROGRESSION ( 12 FDA reports)
HAEMATURIA ( 12 FDA reports)
MENTAL STATUS CHANGES ( 12 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 12 FDA reports)
THYROID NEOPLASM ( 12 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 12 FDA reports)
ASCITES ( 11 FDA reports)
CEREBRAL HAEMORRHAGE ( 11 FDA reports)
CHILLS ( 11 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 11 FDA reports)
COUGH ( 11 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 11 FDA reports)
HAEMOGLOBIN DECREASED ( 11 FDA reports)
HAEMOPTYSIS ( 11 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 11 FDA reports)
ILEUS ( 11 FDA reports)
LOSS OF CONSCIOUSNESS ( 11 FDA reports)
NO THERAPEUTIC RESPONSE ( 11 FDA reports)
PAIN ( 11 FDA reports)
PLATELET COUNT DECREASED ( 11 FDA reports)
PNEUMONIA LEGIONELLA ( 11 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 11 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 11 FDA reports)
PULMONARY HYPERTENSION ( 11 FDA reports)
STEM CELL TRANSPLANT ( 11 FDA reports)
ZYGOMYCOSIS ( 11 FDA reports)
ACOUSTIC NEUROMA ( 10 FDA reports)
BASAL CELL CARCINOMA ( 10 FDA reports)
BREAST MASS ( 10 FDA reports)
CELLULITIS ( 10 FDA reports)
CIRCULATORY COLLAPSE ( 10 FDA reports)
ENTEROCOCCAL INFECTION ( 10 FDA reports)
GASTROENTERITIS NOROVIRUS ( 10 FDA reports)
HEPATIC ENZYME INCREASED ( 10 FDA reports)
HEPATITIS ACUTE ( 10 FDA reports)
HUMAN POLYOMAVIRUS INFECTION ( 10 FDA reports)
LYMPHADENOPATHY ( 10 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 10 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 10 FDA reports)
MICROANGIOPATHY ( 10 FDA reports)
NEPHRITIS AUTOIMMUNE ( 10 FDA reports)
NEPHROTIC SYNDROME ( 10 FDA reports)
PERIPHERAL T-CELL LYMPHOMA UNSPECIFIED ( 10 FDA reports)
PROTEINURIA ( 10 FDA reports)
PULMONARY EMBOLISM ( 10 FDA reports)
RESPIRATORY TRACT INFECTION ( 10 FDA reports)
SINUSITIS ( 10 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 10 FDA reports)
SYNCOPE ( 10 FDA reports)
ACANTHAMOEBA INFECTION ( 9 FDA reports)
ANOREXIA ( 9 FDA reports)
ATRIAL FIBRILLATION ( 9 FDA reports)
BRONCHITIS ( 9 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 9 FDA reports)
ENDOCRINE OPHTHALMOPATHY ( 9 FDA reports)
FUNGAEMIA ( 9 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 9 FDA reports)
HEPATOTOXICITY ( 9 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 9 FDA reports)
HYPONATRAEMIA ( 9 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 9 FDA reports)
LYMPHOMA TRANSFORMATION ( 9 FDA reports)
MEGAKARYOCYTES INCREASED ( 9 FDA reports)
NOCARDIOSIS ( 9 FDA reports)
SHOCK ( 9 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 8 FDA reports)
ANORECTAL CELLULITIS ( 8 FDA reports)
BACTERIAL SEPSIS ( 8 FDA reports)
BLOOD POTASSIUM DECREASED ( 8 FDA reports)
CANDIDA PNEUMONIA ( 8 FDA reports)
CHEST PAIN ( 8 FDA reports)
CYSTITIS HAEMORRHAGIC ( 8 FDA reports)
DECREASED APPETITE ( 8 FDA reports)
DRUG INTERACTION ( 8 FDA reports)
ECZEMA ( 8 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 8 FDA reports)
FACTOR VIII DEFICIENCY ( 8 FDA reports)
FLANK PAIN ( 8 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 8 FDA reports)
GENITOURINARY TRACT NEOPLASM ( 8 FDA reports)
GLOMERULONEPHROPATHY ( 8 FDA reports)
HAEMORRHAGIC ANAEMIA ( 8 FDA reports)
HYPOXIA ( 8 FDA reports)
IDIOPATHIC PNEUMONIA SYNDROME ( 8 FDA reports)
INJECTION SITE ERYTHEMA ( 8 FDA reports)
INJECTION SITE OEDEMA ( 8 FDA reports)
INJECTION SITE PAIN ( 8 FDA reports)
INJECTION SITE PRURITUS ( 8 FDA reports)
INJECTION SITE REACTION ( 8 FDA reports)
METAPNEUMOVIRUS INFECTION ( 8 FDA reports)
PNEUMONIA HERPES VIRAL ( 8 FDA reports)
PNEUMONIA INFLUENZAL ( 8 FDA reports)
PNEUMONIA PARAINFLUENZAE VIRAL ( 8 FDA reports)
RENAL TUBULAR NECROSIS ( 8 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 8 FDA reports)
THYROID CANCER ( 8 FDA reports)
VAGINAL HAEMORRHAGE ( 8 FDA reports)
VIRAL TEST POSITIVE ( 8 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 8 FDA reports)
ABDOMINAL DISTENSION ( 7 FDA reports)
ACUTE ABDOMEN ( 7 FDA reports)
AMNESIA ( 7 FDA reports)
BLOOD BILIRUBIN INCREASED ( 7 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 7 FDA reports)
CHEST DISCOMFORT ( 7 FDA reports)
COLON CANCER METASTATIC ( 7 FDA reports)
CONDITION AGGRAVATED ( 7 FDA reports)
CSF TEST ABNORMAL ( 7 FDA reports)
DISSEMINATED TUBERCULOSIS ( 7 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 7 FDA reports)
HEPATIC CIRRHOSIS ( 7 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 7 FDA reports)
LETHARGY ( 7 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 7 FDA reports)
MUCORMYCOSIS ( 7 FDA reports)
OROPHARYNGEAL PAIN ( 7 FDA reports)
PERINEAL ULCERATION ( 7 FDA reports)
SINUS TACHYCARDIA ( 7 FDA reports)
STENOTROPHOMONAS INFECTION ( 7 FDA reports)
VIRAEMIA ( 7 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 6 FDA reports)
ACUTE RESPIRATORY FAILURE ( 6 FDA reports)
ANGINA PECTORIS ( 6 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 6 FDA reports)
APHASIA ( 6 FDA reports)
APPENDICITIS ( 6 FDA reports)
ASPIRATION BONE MARROW ABNORMAL ( 6 FDA reports)
AUTOIMMUNE PANCYTOPENIA ( 6 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 6 FDA reports)
CARDIO-RESPIRATORY ARREST ( 6 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 6 FDA reports)
CEREBRAL ASPERGILLOSIS ( 6 FDA reports)
CLOSTRIDIAL INFECTION ( 6 FDA reports)
DYSPHAGIA ( 6 FDA reports)
ENCEPHALOPATHY ( 6 FDA reports)
ENGRAFT FAILURE ( 6 FDA reports)
GALLBLADDER DISORDER ( 6 FDA reports)
GENE MUTATION ( 6 FDA reports)
GOITRE ( 6 FDA reports)
GRAFT VERSUS HOST DISEASE IN SKIN ( 6 FDA reports)
GUILLAIN-BARRE SYNDROME ( 6 FDA reports)
LABYRINTHITIS ( 6 FDA reports)
LEUKAEMIA RECURRENT ( 6 FDA reports)
LUNG NEOPLASM ( 6 FDA reports)
MICROSPORIDIA INFECTION ( 6 FDA reports)
MYELOFIBROSIS ( 6 FDA reports)
NEUTROPENIC SEPSIS ( 6 FDA reports)
PEPTIC ULCER ( 6 FDA reports)
PERIORBITAL OEDEMA ( 6 FDA reports)
PERITONITIS ( 6 FDA reports)
PLATELET COUNT ABNORMAL ( 6 FDA reports)
RED BLOOD CELL ABNORMALITY ( 6 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 6 FDA reports)
SOMNOLENCE ( 6 FDA reports)
STAPHYLOCOCCAL INFECTION ( 6 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 6 FDA reports)
T-CELL LYMPHOMA RECURRENT ( 6 FDA reports)
THROMBOPHLEBITIS ( 6 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 6 FDA reports)
TREMOR ( 6 FDA reports)
VIRAL INFECTION ( 6 FDA reports)
WEIGHT INCREASED ( 6 FDA reports)
ABNORMAL BEHAVIOUR ( 5 FDA reports)
ABSCESS ( 5 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 5 FDA reports)
AGITATION ( 5 FDA reports)
BACTERAEMIA ( 5 FDA reports)
BLADDER CANCER ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 5 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 5 FDA reports)
COLITIS ( 5 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 5 FDA reports)
DIPLOPIA ( 5 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 5 FDA reports)
FIBROSIS ( 5 FDA reports)
GRAFT LOSS ( 5 FDA reports)
HAEMODIALYSIS ( 5 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 5 FDA reports)
HAEMORRHAGIC STROKE ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HEPATIC FIBROSIS ( 5 FDA reports)
HYDROCEPHALUS ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
LARGE INTESTINE PERFORATION ( 5 FDA reports)
LEUKOENCEPHALOPATHY ( 5 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 5 FDA reports)
MACULE ( 5 FDA reports)
MALAISE ( 5 FDA reports)
MENINGITIS ( 5 FDA reports)
MENORRHAGIA ( 5 FDA reports)
MYCOBACTERIAL INFECTION ( 5 FDA reports)
PERICARDIAL EFFUSION ( 5 FDA reports)
PNEUMONIA ADENOVIRAL ( 5 FDA reports)
POLYCHROMASIA ( 5 FDA reports)
PULMONARY HAEMORRHAGE ( 5 FDA reports)
PULMONARY SEPSIS ( 5 FDA reports)
RASH GENERALISED ( 5 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 5 FDA reports)
RETICULOCYTOSIS ( 5 FDA reports)
SPHEROCYTIC ANAEMIA ( 5 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 5 FDA reports)
SYSTEMIC MYCOSIS ( 5 FDA reports)
TOXOPLASMOSIS ( 5 FDA reports)
TRANSPLANT FAILURE ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
VASCULITIS ( 5 FDA reports)
ACID FAST BACILLI INFECTION ( 4 FDA reports)
ACINETOBACTER INFECTION ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 4 FDA reports)
ADVERSE EVENT ( 4 FDA reports)
ALTERNARIA INFECTION ( 4 FDA reports)
ANAPHYLACTOID REACTION ( 4 FDA reports)
ANGIOIMMUNOBLASTIC T-CELL LYMPHOMA RECURRENT ( 4 FDA reports)
ASPERGILLOMA ( 4 FDA reports)
B-CELL LYMPHOMA ( 4 FDA reports)
BRAIN STEM SYNDROME ( 4 FDA reports)
BRONCHOPNEUMONIA ( 4 FDA reports)
CALCULUS URINARY ( 4 FDA reports)
CANDIDA SEPSIS ( 4 FDA reports)
CANDIDIASIS ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 4 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 4 FDA reports)
CERVIX DISORDER ( 4 FDA reports)
CHIMERISM ( 4 FDA reports)
CHORIORETINITIS ( 4 FDA reports)
CORYNEBACTERIUM INFECTION ( 4 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 4 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 4 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
DERMAL CYST ( 4 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 4 FDA reports)
DRUG RESISTANCE ( 4 FDA reports)
DYSARTHRIA ( 4 FDA reports)
DYSURIA ( 4 FDA reports)
EPILEPSY ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
ESCHERICHIA INFECTION ( 4 FDA reports)
EYE DISORDER ( 4 FDA reports)
FUNGAL SEPSIS ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
GASTROENTERITIS ADENOVIRUS ( 4 FDA reports)
GASTROENTERITIS VIRAL ( 4 FDA reports)
GASTROINTESTINAL PERFORATION ( 4 FDA reports)
GRAFT VERSUS HOST DISEASE IN INTESTINE ( 4 FDA reports)
GRAFT VERSUS HOST DISEASE IN LUNG ( 4 FDA reports)
HEPATITIS B ( 4 FDA reports)
HEPATITIS C ( 4 FDA reports)
HYPOPHAGIA ( 4 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
LARGE INTESTINAL ULCER ( 4 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
LUNG CONSOLIDATION ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
MELAENA ( 4 FDA reports)
MENINGITIS BACTERIAL ( 4 FDA reports)
METASTASES TO LYMPH NODES ( 4 FDA reports)
MICROCOCCUS INFECTION ( 4 FDA reports)
MOOD SWINGS ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
MYCOBACTERIUM ABSCESSUS INFECTION ( 4 FDA reports)
MYCOBACTERIUM KANSASII INFECTION ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
NEPHROLITHIASIS ( 4 FDA reports)
NEUROTOXICITY ( 4 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
OPPORTUNISTIC INFECTION ( 4 FDA reports)
ORAL DISORDER ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
PAPILLOMA VIRAL INFECTION ( 4 FDA reports)
PAPULE ( 4 FDA reports)
PEMPHIGOID ( 4 FDA reports)
PERICARDITIS FUNGAL ( 4 FDA reports)
PNEUMONIA ASPIRATION ( 4 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 4 FDA reports)
PNEUMONIA FUNGAL ( 4 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 4 FDA reports)
PORTAL HYPERTENSION ( 4 FDA reports)
PREGNANCY ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
RETINAL HAEMORRHAGE ( 4 FDA reports)
RHONCHI ( 4 FDA reports)
SKIN CANCER ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
SKIN TOXICITY ( 4 FDA reports)
SUDDEN CARDIAC DEATH ( 4 FDA reports)
THYROIDITIS ( 4 FDA reports)
TRACHEITIS ( 4 FDA reports)
VULVOVAGINAL HUMAN PAPILLOMA VIRUS INFECTION ( 4 FDA reports)
ABDOMINAL MASS ( 3 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
ALVEOLITIS FIBROSING ( 3 FDA reports)
ANGIOSARCOMA ( 3 FDA reports)
ANTI-GLOMERULAR BASEMENT MEMBRANE ANTIBODY POSITIVE ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
ATAXIA ( 3 FDA reports)
B-CELL UNCLASSIFIABLE LYMPHOMA HIGH GRADE ( 3 FDA reports)
BLADDER DISORDER ( 3 FDA reports)
BLADDER PAPILLOMA ( 3 FDA reports)
BLOOD COUNT ABNORMAL ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 3 FDA reports)
CACHEXIA ( 3 FDA reports)
CAPILLARY LEAK SYNDROME ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 3 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 3 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 3 FDA reports)
CUSHING'S SYNDROME ( 3 FDA reports)
DEMENTIA ( 3 FDA reports)
DEPRESSED MOOD ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DISEASE RECURRENCE ( 3 FDA reports)
DRUG ABUSE ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
EAR INFECTION ( 3 FDA reports)
ECHOLALIA ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
ENTEROCOCCAL SEPSIS ( 3 FDA reports)
ERYSIPELOID ( 3 FDA reports)
ERYTHEMA MULTIFORME ( 3 FDA reports)
FUSARIUM INFECTION ( 3 FDA reports)
GASTROINTESTINAL INFECTION ( 3 FDA reports)
GASTROINTESTINAL NECROSIS ( 3 FDA reports)
GASTROINTESTINAL TOXICITY ( 3 FDA reports)
GLOMERULONEPHRITIS ( 3 FDA reports)
GRAFT INFECTION ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HERPES ZOSTER DISSEMINATED ( 3 FDA reports)
IMMUNOSUPPRESSION ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
JAW DISORDER ( 3 FDA reports)
JC VIRUS INFECTION ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LOCAL SWELLING ( 3 FDA reports)
LUNG ABSCESS ( 3 FDA reports)
METABOLIC DISORDER ( 3 FDA reports)
METASTASES TO LUNG ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
NEPHRITIS ( 3 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 3 FDA reports)
OPHTHALMOPLEGIA ( 3 FDA reports)
ORGANISING PNEUMONIA ( 3 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 3 FDA reports)
PARVOVIRUS INFECTION ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
PULMONARY MYCOSIS ( 3 FDA reports)
PURPURA ( 3 FDA reports)
PURULENCE ( 3 FDA reports)
RETINITIS ( 3 FDA reports)
RHINITIS ( 3 FDA reports)
RHINORRHOEA ( 3 FDA reports)
SARCOIDOSIS ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
SPLENECTOMY ( 3 FDA reports)
SPLENOMEGALY ( 3 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
SUBSTANCE ABUSE ( 3 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 3 FDA reports)
THYROID DISORDER ( 3 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 3 FDA reports)
TRANSFUSION MICROCHIMERISM ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
VARICES OESOPHAGEAL ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ACTINOMYCOSIS ( 2 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
APPENDICECTOMY ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
BACILLUS INFECTION ( 2 FDA reports)
BACTERIAL TEST POSITIVE ( 2 FDA reports)
BENIGN NEOPLASM ( 2 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 2 FDA reports)
BLADDER PAIN ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BRAIN NEOPLASM ( 2 FDA reports)
BREAST CANCER FEMALE ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COLLAPSE OF LUNG ( 2 FDA reports)
CONGENITAL CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 2 FDA reports)
CSF BACTERIA IDENTIFIED ( 2 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIPLEGIA ( 2 FDA reports)
DUODENITIS ( 2 FDA reports)
ENCEPHALITIS VIRAL ( 2 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 2 FDA reports)
EROSIVE DUODENITIS ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTROENTERITIS SALMONELLA ( 2 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GOODPASTURE'S SYNDROME ( 2 FDA reports)
GRAFT THROMBOSIS ( 2 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMATOTOXICITY ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HISTOPLASMOSIS ( 2 FDA reports)
HYPERCHLORHYDRIA ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
INTESTINE TRANSPLANT REJECTION ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LUNG CYST ( 2 FDA reports)
LUNG TRANSPLANT REJECTION ( 2 FDA reports)
LYMPHOHISTIOCYTOSIS ( 2 FDA reports)
MALIGNANT MELANOMA IN SITU ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METHYLOBACTERIUM INFECTION ( 2 FDA reports)
MISCARRIAGE OF PARTNER ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MYCOBACTERIUM CHELONEI INFECTION ( 2 FDA reports)
MYELITIS ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 2 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NOSOCOMIAL INFECTION ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
OROPHARYNGEAL BLISTERING ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PANCREATECTOMY ( 2 FDA reports)
PATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
PEMPHIGUS ( 2 FDA reports)
PERINEPHRIC ABSCESS ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
POST HERPETIC NEURALGIA ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
PREGNANCY OF PARTNER ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PULMONARY HILUM MASS ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RENAL TRANSPLANT ( 2 FDA reports)
RESPIRATORY MONILIASIS ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
SCEDOSPORIUM INFECTION ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SINUS ARRHYTHMIA ( 2 FDA reports)
SINUS CONGESTION ( 2 FDA reports)
SKIN PAPILLOMA ( 2 FDA reports)
SOFT TISSUE INFECTION ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 2 FDA reports)
STEATORRHOEA ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
STRONGYLOIDIASIS ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
T-CELL LYMPHOMA ( 2 FDA reports)
T-CELL PROLYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
THYROIDECTOMY ( 2 FDA reports)
TOOTH INFECTION ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 2 FDA reports)
TRICHOSPORON INFECTION ( 2 FDA reports)
TYPE 1 DIABETES MELLITUS ( 2 FDA reports)
URINARY TRACT OBSTRUCTION ( 2 FDA reports)
VASCULAR PSEUDOANEURYSM ( 2 FDA reports)
VIRAL MYOCARDITIS ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
VULVAL CANCER ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE CHEST SYNDROME ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIOSARCOMA METASTATIC ( 1 FDA reports)
ANGIOTENSIN CONVERTING ENZYME DECREASED ( 1 FDA reports)
ANTI-THYROID ANTIBODY ( 1 FDA reports)
ANTI-THYROID ANTIBODY POSITIVE ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLAST CELL PROLIFERATION ( 1 FDA reports)
BLASTOMYCOSIS ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW TRANSPLANT REJECTION ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRAIN MASS ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CANDIDURIA ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHOLECYSTITIS INFECTIVE ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHROMOSOMAL DELETION ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CITROBACTER INFECTION ( 1 FDA reports)
CLONUS ( 1 FDA reports)
COCCIDIOIDOMYCOSIS ( 1 FDA reports)
COLD AGGLUTININS POSITIVE ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CRANIAL NERVE PARALYSIS ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CRYPTOCOCCOSIS ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DESMOID TUMOUR ( 1 FDA reports)
DISSEMINATED LARGE CELL LYMPHOMA ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DUCHENNE MUSCULAR DYSTROPHY ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENTEROBACTER BACTERAEMIA ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EVAN'S SYNDROME ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FALL ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FUNGAL ENDOCARDITIS ( 1 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC SIDEROSIS ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HEPATOBILIARY DISEASE ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOGLOBULINAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
ILIAC ARTERY THROMBOSIS ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INFECTION PROTOZOAL ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JC VIRUS TEST POSITIVE ( 1 FDA reports)
JUGULAR VEIN DISTENSION ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MASTOID DISORDER ( 1 FDA reports)
MEDIASTINITIS ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENINGITIS TUBERCULOUS ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL INFECTION ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYCOBACTERIUM FORTUITUM INFECTION ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
ORTHOPEDIC PROCEDURE ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PARASITIC TEST POSITIVE ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PNEUMATOSIS INTESTINALIS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POST PROCEDURAL DISCHARGE ( 1 FDA reports)
PREMATURE MENOPAUSE ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRIMARY HYPOTHYROIDISM ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RED BLOOD CELL AGGLUTINATION ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RENAL VEIN THROMBOSIS ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SOFT TISSUE NEOPLASM ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
SUPERINFECTION BACTERIAL ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRIGEMINAL NEURALGIA ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
VANISHING BILE DUCT SYNDROME ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VARICELLA VIRUS TEST POSITIVE ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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