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

PNEUMONIA ( 35 FDA reports)
ANAEMIA ( 21 FDA reports)
INTERSTITIAL LUNG DISEASE ( 21 FDA reports)
PYREXIA ( 21 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 21 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 18 FDA reports)
FEBRILE NEUTROPENIA ( 18 FDA reports)
BONE MARROW FAILURE ( 16 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 16 FDA reports)
NEOPLASM MALIGNANT ( 15 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 14 FDA reports)
BONE MARROW DEPRESSION ( 14 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 14 FDA reports)
OSTEONECROSIS ( 14 FDA reports)
VOMITING ( 14 FDA reports)
DRUG INTERACTION ( 13 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 12 FDA reports)
BONE DISORDER ( 12 FDA reports)
CARDIAC FAILURE ( 12 FDA reports)
METASTASES TO BONE ( 12 FDA reports)
MULTIPLE MYELOMA ( 12 FDA reports)
MYELODYSPLASTIC SYNDROME ( 12 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 12 FDA reports)
DEATH ( 11 FDA reports)
DIARRHOEA ( 11 FDA reports)
NEUROBLASTOMA ( 11 FDA reports)
NEUTROPHIL COUNT DECREASED ( 11 FDA reports)
PLATELET COUNT DECREASED ( 11 FDA reports)
THROMBOCYTOPENIA ( 11 FDA reports)
METASTASES TO LIVER ( 10 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 9 FDA reports)
CEREBRAL INFARCTION ( 9 FDA reports)
CONSTIPATION ( 9 FDA reports)
HERPES ZOSTER ( 9 FDA reports)
LIVER DISORDER ( 9 FDA reports)
MALAISE ( 9 FDA reports)
MUSCULAR WEAKNESS ( 9 FDA reports)
PLEURAL EFFUSION ( 9 FDA reports)
RESPIRATORY FAILURE ( 9 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 8 FDA reports)
HAEMOGLOBIN DECREASED ( 8 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 8 FDA reports)
HEPATITIS B ( 8 FDA reports)
HYPERTENSION ( 8 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 8 FDA reports)
NEUTROPENIA ( 8 FDA reports)
PANCYTOPENIA ( 8 FDA reports)
TOOTH EXTRACTION ( 8 FDA reports)
BONE PAIN ( 7 FDA reports)
CARDIAC FAILURE ACUTE ( 7 FDA reports)
DYSPNOEA ( 7 FDA reports)
HEADACHE ( 7 FDA reports)
HYPONATRAEMIA ( 7 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 7 FDA reports)
MYALGIA ( 7 FDA reports)
NEUROPATHY PERIPHERAL ( 7 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 7 FDA reports)
SEPSIS ( 7 FDA reports)
SEPTIC SHOCK ( 7 FDA reports)
TUMOUR LYSIS SYNDROME ( 7 FDA reports)
ATRIAL FIBRILLATION ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 6 FDA reports)
CARDIOMEGALY ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
DISEASE PROGRESSION ( 6 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
HEPATIC FAILURE ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 6 FDA reports)
MULTI-ORGAN FAILURE ( 6 FDA reports)
OSTEOMYELITIS ( 6 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 5 FDA reports)
ANOREXIA ( 5 FDA reports)
CARDIOMYOPATHY ( 5 FDA reports)
ENCEPHALOPATHY ( 5 FDA reports)
GINGIVAL BLEEDING ( 5 FDA reports)
HAEMORRHAGIC DIATHESIS ( 5 FDA reports)
LEUKAEMIA ( 5 FDA reports)
LIVER ABSCESS ( 5 FDA reports)
METASTASES TO LYMPH NODES ( 5 FDA reports)
NEOPLASM RECURRENCE ( 5 FDA reports)
RENAL DISORDER ( 5 FDA reports)
ADVERSE EVENT ( 4 FDA reports)
AIDS ENCEPHALOPATHY ( 4 FDA reports)
ALLERGIC CYSTITIS ( 4 FDA reports)
APPENDICITIS ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CYSTITIS HAEMORRHAGIC ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 4 FDA reports)
GINGIVITIS ( 4 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 4 FDA reports)
HEPATIC NEOPLASM MALIGNANT RECURRENT ( 4 FDA reports)
HEPATITIS ( 4 FDA reports)
HYPERBILIRUBINAEMIA ( 4 FDA reports)
IIIRD NERVE PARALYSIS ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
MELAENA ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
METASTASES TO LUNG ( 4 FDA reports)
METASTASES TO SPINE ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
OPPORTUNISTIC INFECTION ( 4 FDA reports)
ORGANISING PNEUMONIA ( 4 FDA reports)
OSTEONECROSIS OF JAW ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PAIN ( 4 FDA reports)
PARAPLEGIA ( 4 FDA reports)
PERIODONTAL DISEASE ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
SEQUESTRECTOMY ( 4 FDA reports)
SPINAL CORD PARALYSIS ( 4 FDA reports)
STOMATITIS ( 4 FDA reports)
THROMBOSIS ( 4 FDA reports)
TOOTHACHE ( 4 FDA reports)
TUMOUR EMBOLISM ( 4 FDA reports)
AMYLOIDOSIS ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
BLOOD COUNT ABNORMAL ( 3 FDA reports)
BLOOD SODIUM ABNORMAL ( 3 FDA reports)
BLOOD UREA ABNORMAL ( 3 FDA reports)
BREAST CANCER RECURRENT ( 3 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
DRUG RESISTANCE ( 3 FDA reports)
ENDOTOXIC SHOCK ( 3 FDA reports)
ENTEROBACTER SEPSIS ( 3 FDA reports)
GASTROENTERITIS BACILLUS ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HALLUCINATION, AUDITORY ( 3 FDA reports)
HEPATITIS C ( 3 FDA reports)
HEPATITIS FULMINANT ( 3 FDA reports)
HYPERLIPIDAEMIA ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
ILEUS ( 3 FDA reports)
IMPAIRED HEALING ( 3 FDA reports)
LARGE INTESTINE CARCINOMA ( 3 FDA reports)
MONOPLEGIA ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
NERVE INJURY ( 3 FDA reports)
OESOPHAGEAL CARCINOMA ( 3 FDA reports)
OLFACTORY NERVE DISORDER ( 3 FDA reports)
ORAL NEOPLASM ( 3 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
PROTEIN URINE PRESENT ( 3 FDA reports)
PULMONARY HYPERTENSION ( 3 FDA reports)
PURULENT DISCHARGE ( 3 FDA reports)
RENAL FAILURE ACUTE ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
TRISMUS ( 3 FDA reports)
UTERINE LEIOMYOMA ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
X-RAY ABNORMAL ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ACUTE LUNG INJURY ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BONE SARCOMA ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BRAIN NEOPLASM ( 2 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIAC TAMPONADE ( 2 FDA reports)
CEREBELLAR INFARCTION ( 2 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHRONIC EOSINOPHILIC LEUKAEMIA ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
COUGH ( 2 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 2 FDA reports)
DEBRIDEMENT ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DENTAL CARE ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIABETES INSIPIDUS ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
EMPYEMA ( 2 FDA reports)
EWING'S SARCOMA ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
GINGIVAL CANCER ( 2 FDA reports)
GINGIVAL DISCOLOURATION ( 2 FDA reports)
GINGIVAL OPERATION ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
JAW OPERATION ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
METASTASIS ( 2 FDA reports)
MYELITIS ( 2 FDA reports)
NASAL SINUS CANCER ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PNEUMATOSIS INTESTINALIS ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PRIMARY SEQUESTRUM ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PYLORIC STENOSIS ( 2 FDA reports)
RADIAL NERVE PALSY ( 2 FDA reports)
RASH ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
SWELLING ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
THERAPEUTIC PROCEDURE ( 2 FDA reports)
TONIC CONVULSION ( 2 FDA reports)
TOOTH ABSCESS ( 2 FDA reports)
TOOTH DISORDER ( 2 FDA reports)
TOOTH LOSS ( 2 FDA reports)
TREMOR ( 2 FDA reports)
TUMOUR ULCERATION ( 2 FDA reports)
URETERIC CANCER ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
WOUND CLOSURE ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE LEUKAEMIA ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
BASE EXCESS ( 1 FDA reports)
BILIARY FISTULA ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CEREBELLAR TUMOUR ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE III ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDOCARDITIS NONINFECTIVE ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EWING'S SARCOMA METASTATIC ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYELID DISORDER ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS BACTERIAL ( 1 FDA reports)
GASTROINTESTINAL FISTULA ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEPATIC TRAUMA ( 1 FDA reports)
HEPATITIS ALCOHOLIC ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NIPPLE PAIN ( 1 FDA reports)
NIPPLE SWELLING ( 1 FDA reports)
NODULE ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PRECURSOR T-LYMPHOBLASTIC LYMPHOMA/LEUKAEMIA ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PRIMITIVE NEUROECTODERMAL TUMOUR ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 1 FDA reports)
SECONDARY IMMUNODEFICIENCY ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
THORACIC HAEMORRHAGE ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WEIGHT ABNORMAL ( 1 FDA reports)
WISDOM TEETH REMOVAL ( 1 FDA reports)

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