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

VOMITING ( 18 FDA reports)
DRUG INTERACTION ( 17 FDA reports)
PYREXIA ( 13 FDA reports)
DRUG INEFFECTIVE ( 12 FDA reports)
PULMONARY TUBERCULOSIS ( 11 FDA reports)
ARRHYTHMIA ( 10 FDA reports)
BASAL CELL CARCINOMA ( 10 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 10 FDA reports)
DIARRHOEA ( 9 FDA reports)
DYSPNOEA ( 9 FDA reports)
TUBERCULOSIS ( 9 FDA reports)
CYANOSIS ( 8 FDA reports)
DIZZINESS ( 8 FDA reports)
METABOLIC ACIDOSIS ( 8 FDA reports)
NAUSEA ( 8 FDA reports)
RENAL FAILURE ( 8 FDA reports)
RESPIRATORY FAILURE ( 8 FDA reports)
ATRIAL FIBRILLATION ( 7 FDA reports)
DISORIENTATION ( 7 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 7 FDA reports)
GRAND MAL CONVULSION ( 7 FDA reports)
HAEMOGLOBIN DECREASED ( 7 FDA reports)
LOSS OF CONSCIOUSNESS ( 7 FDA reports)
PANCYTOPENIA ( 7 FDA reports)
SEPTIC SHOCK ( 7 FDA reports)
SEROTONIN SYNDROME ( 7 FDA reports)
BREAST CANCER ( 6 FDA reports)
CARDIAC FAILURE ( 6 FDA reports)
FALL ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
RESPIRATORY TRACT INFECTION ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
DEEP VEIN THROMBOSIS ( 5 FDA reports)
DISSEMINATED TUBERCULOSIS ( 5 FDA reports)
GRAFT VERSUS HOST DISEASE ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
HEPATOMEGALY ( 5 FDA reports)
HYPERGLYCAEMIA ( 5 FDA reports)
HYPERHIDROSIS ( 5 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
RESPIRATORY DISTRESS ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
TREATMENT NONCOMPLIANCE ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
AGEUSIA ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
ANOSMIA ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
BONE MARROW FAILURE ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
INFECTION ( 4 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 4 FDA reports)
ISCHAEMIC STROKE ( 4 FDA reports)
LYMPHOMA ( 4 FDA reports)
MALAISE ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
ODYNOPHAGIA ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
PNEUMONIA BACTERIAL ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 4 FDA reports)
SKIN ODOUR ABNORMAL ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 4 FDA reports)
VIRAL INFECTION ( 4 FDA reports)
ABSCESS ( 3 FDA reports)
ALLERGIC TRANSFUSION REACTION ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ASCITES ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BONE TUBERCULOSIS ( 3 FDA reports)
CAPILLARY LEAK SYNDROME ( 3 FDA reports)
CEREBROVASCULAR DISORDER ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
CONGENITAL ANOMALY ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
ESCHERICHIA INFECTION ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
INJECTION SITE INDURATION ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
NODAL RHYTHM ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
PERICARDIAL HAEMORRHAGE ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RESPIRATORY DEPRESSION ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
UTERINE CANCER ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
APLASIA ( 2 FDA reports)
APPENDICITIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC VALVE DISEASE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
ENTEROCOCCAL SEPSIS ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
ERYTHRODERMIC PSORIASIS ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HEPATIC CYST ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
LISTERIA ENCEPHALITIS ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MENINGITIS LISTERIA ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYCOSIS FUNGOIDES ( 2 FDA reports)
MYOSITIS ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
ORAL INFECTION ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
OSTEITIS DEFORMANS ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PNEUMONIA KLEBSIELLA ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL TUBERCULOSIS ( 2 FDA reports)
SIDEROBLASTIC ANAEMIA ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
TIBIA FRACTURE ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACNE CONGLOBATA ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ASTROCYTOMA MALIGNANT ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER PAPILLOMA ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
CARCINOID TUMOUR OF THE STOMACH ( 1 FDA reports)
CARDIAC ABLATION ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CATHETER CULTURE POSITIVE ( 1 FDA reports)
CEMENTOPLASTY ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLON CANCER STAGE IV ( 1 FDA reports)
COUGH ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CUTANEOUS VASCULITIS ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROENTERITIS ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENITAL TRACT INFLAMMATION ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
KERATOACANTHOMA ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LEUKAEMIA PLASMACYTIC ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPH NODE TUBERCULOSIS ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MALIGNANT NEOPLASM OF AMPULLA OF VATER ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUROSENSORY HYPOACUSIS ( 1 FDA reports)
NIGHT BLINDNESS ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PATELLA FRACTURE ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PNEUMONIA LEGIONELLA ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RASH ( 1 FDA reports)
REFRACTORY ANAEMIA WITH RINGED SIDEROBLASTS ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHEUMATOID FACTOR INCREASED ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 1 FDA reports)
SALPINGITIS ( 1 FDA reports)
SEBORRHOEIC DERMATITIS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN ULCER HAEMORRHAGE ( 1 FDA reports)
SPINAL COLUMN INJURY ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUPERFICIAL SPREADING MELANOMA STAGE II ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYNOVECTOMY ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
TENOSYNOVITIS STENOSANS ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VITAMIN A DEFICIENCY ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WRIST SURGERY ( 1 FDA reports)

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