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

FEBRILE NEUTROPENIA ( 33 FDA reports)
DYSPNOEA ( 21 FDA reports)
PYREXIA ( 20 FDA reports)
DIARRHOEA ( 17 FDA reports)
OSTEONECROSIS ( 15 FDA reports)
INFECTION ( 13 FDA reports)
PLEURAL EFFUSION ( 12 FDA reports)
SEPSIS ( 12 FDA reports)
BONE DISORDER ( 11 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 11 FDA reports)
STAPHYLOCOCCAL INFECTION ( 11 FDA reports)
ARTHRALGIA ( 10 FDA reports)
BONE PAIN ( 10 FDA reports)
NAUSEA ( 10 FDA reports)
VOMITING ( 10 FDA reports)
HYPOTENSION ( 9 FDA reports)
RENAL FAILURE ( 9 FDA reports)
TOOTH EXTRACTION ( 9 FDA reports)
DRUG INEFFECTIVE ( 8 FDA reports)
GINGIVAL SWELLING ( 8 FDA reports)
NEUTROPENIA ( 8 FDA reports)
PNEUMONIA ( 8 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 8 FDA reports)
ANAEMIA ( 7 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 7 FDA reports)
DEHYDRATION ( 7 FDA reports)
NEUTROPHIL COUNT DECREASED ( 7 FDA reports)
PANCYTOPENIA ( 7 FDA reports)
PLEURODESIS ( 7 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
BACK PAIN ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 6 FDA reports)
BLOOD POTASSIUM DECREASED ( 6 FDA reports)
BLOOD SODIUM DECREASED ( 6 FDA reports)
BONE DEBRIDEMENT ( 6 FDA reports)
DRUG INTOLERANCE ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
OSTEOMYELITIS ( 6 FDA reports)
PAIN ( 6 FDA reports)
PAIN IN JAW ( 6 FDA reports)
PERFORMANCE STATUS DECREASED ( 6 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 6 FDA reports)
RIB FRACTURE ( 6 FDA reports)
SEPTIC SHOCK ( 6 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 5 FDA reports)
CANDIDIASIS ( 5 FDA reports)
LUNG DISORDER ( 5 FDA reports)
ORAL DISCOMFORT ( 5 FDA reports)
PRIMARY SEQUESTRUM ( 5 FDA reports)
RASH ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
ALOPECIA ( 4 FDA reports)
ALVEOLOPLASTY ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
BONE OPERATION ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
CARDIOMYOPATHY ( 4 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 4 FDA reports)
CHILLS ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
ERECTILE DYSFUNCTION ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
JAW OPERATION ( 4 FDA reports)
MUCOSAL INFLAMMATION ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
PNEUMOTHORAX ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
SOFT TISSUE INFLAMMATION ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
TENDERNESS ( 4 FDA reports)
TOOTH ABSCESS ( 4 FDA reports)
ABSCESS ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BONE LESION ( 3 FDA reports)
CACHEXIA ( 3 FDA reports)
CATHETER REMOVAL ( 3 FDA reports)
DEATH ( 3 FDA reports)
ENCEPHALITIS ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
IMPAIRED HEALING ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MASTICATION DISORDER ( 3 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
NEOPLASM RECURRENCE ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 3 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 3 FDA reports)
PLASMACYTOMA ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
SPINAL CORD COMPRESSION ( 3 FDA reports)
STEM CELL TRANSPLANT ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
TOOTH DISORDER ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BONE CYST ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CARDIOTOXICITY ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
COLITIS ( 2 FDA reports)
DEBRIDEMENT ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
EXTRAMEDULLARY HAEMOPOIESIS ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GINGIVAL DISORDER ( 2 FDA reports)
GINGIVAL EROSION ( 2 FDA reports)
GINGIVAL PAIN ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPERPLASIA ( 2 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
INJURY ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LOOSE TOOTH ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
ORAL SURGERY ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
OSTEOPENIA ( 2 FDA reports)
OSTEOSCLEROSIS ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERIRECTAL ABSCESS ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PROCTALGIA ( 2 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PULMONARY TOXICITY ( 2 FDA reports)
PURULENT DISCHARGE ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RETINAL INFARCTION ( 2 FDA reports)
SCAR ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SWELLING ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TONGUE INJURY ( 2 FDA reports)
TOOTH FRACTURE ( 2 FDA reports)
TOOTHACHE ( 2 FDA reports)
TRANSFUSION ( 2 FDA reports)
ULCER ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WOUND COMPLICATION ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ABSCESS JAW ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIOVENOUS GRAFT THROMBOSIS ( 1 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BIOPSY BONE ABNORMAL ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ACID PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INSPIRATORY DECREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BULBAR PALSY ( 1 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CATHETER THROMBOSIS ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
COUGH ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOLOGY ABNORMAL ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DENTAL EXAMINATION ABNORMAL ( 1 FDA reports)
DENTAL OPERATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE III ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
EDENTULOUS ( 1 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FALL ( 1 FDA reports)
FANCONI SYNDROME ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FORCED EXPIRATORY VOLUME ABNORMAL ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GINGIVAL ERYTHEMA ( 1 FDA reports)
GINGIVAL RECESSION ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMOSTASIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
JAW FRACTURE ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIFE EXPECTANCY SHORTENED ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTASES TO SPINE ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEOPLASM OF ORBIT ( 1 FDA reports)
NEUROGENIC SHOCK ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OSTEOLYSIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OVARIAN FAILURE ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PERIODONTAL OPERATION ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROTEIN C DECREASED ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 1 FDA reports)
RHABDOMYOSARCOMA ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SENSITIVITY OF TEETH ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SOFT TISSUE DISORDER ( 1 FDA reports)
SOFT TISSUE INFECTION ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STRONGYLOIDIASIS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
TENSION ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBECTOMY ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENTRICULAR FAILURE ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)

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