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

PNEUMONIA ( 55 FDA reports)
ABNORMAL BEHAVIOUR ( 46 FDA reports)
INTERSTITIAL LUNG DISEASE ( 45 FDA reports)
ANAEMIA ( 30 FDA reports)
PYREXIA ( 30 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 27 FDA reports)
PLEURAL EFFUSION ( 27 FDA reports)
COUGH ( 26 FDA reports)
MALAISE ( 24 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 23 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 20 FDA reports)
NAUSEA ( 19 FDA reports)
DIARRHOEA ( 18 FDA reports)
VOMITING ( 18 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 17 FDA reports)
HALLUCINATION ( 17 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 16 FDA reports)
PLATELET COUNT DECREASED ( 16 FDA reports)
ILEUS ( 15 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 14 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 14 FDA reports)
LIVER DISORDER ( 14 FDA reports)
RASH ( 14 FDA reports)
ASTHMA ( 13 FDA reports)
CARDIAC FAILURE ( 13 FDA reports)
DYSPNOEA ( 13 FDA reports)
NEUTROPHIL COUNT DECREASED ( 13 FDA reports)
NEOPLASM MALIGNANT ( 12 FDA reports)
RENAL IMPAIRMENT ( 11 FDA reports)
SEPSIS ( 11 FDA reports)
STEVENS-JOHNSON SYNDROME ( 11 FDA reports)
NEUTROPENIA ( 10 FDA reports)
RENAL FAILURE ACUTE ( 10 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 10 FDA reports)
AGRANULOCYTOSIS ( 9 FDA reports)
DECREASED APPETITE ( 9 FDA reports)
DEHYDRATION ( 9 FDA reports)
DIZZINESS ( 9 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 9 FDA reports)
ASTHENIA ( 8 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 8 FDA reports)
BLOOD UREA INCREASED ( 8 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 8 FDA reports)
DYSPHONIA ( 8 FDA reports)
FEBRILE NEUTROPENIA ( 8 FDA reports)
HALLUCINATION, AUDITORY ( 8 FDA reports)
HYPOXIA ( 8 FDA reports)
INSOMNIA ( 8 FDA reports)
LUNG DISORDER ( 8 FDA reports)
MEMORY IMPAIRMENT ( 8 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 8 FDA reports)
RHABDOMYOLYSIS ( 8 FDA reports)
AGGRESSION ( 7 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 7 FDA reports)
BLOOD PRESSURE DECREASED ( 7 FDA reports)
BRONCHITIS ( 7 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 7 FDA reports)
DEATH ( 7 FDA reports)
DRUG ERUPTION ( 7 FDA reports)
FALL ( 7 FDA reports)
HYPOGLYCAEMIA ( 7 FDA reports)
NEOPLASM PROGRESSION ( 7 FDA reports)
OEDEMA ( 7 FDA reports)
SEBORRHOEIC DERMATITIS ( 7 FDA reports)
SOMNOLENCE ( 7 FDA reports)
STOMATITIS ( 7 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
EATING DISORDER ( 6 FDA reports)
ERYTHEMA ( 6 FDA reports)
FEELING ABNORMAL ( 6 FDA reports)
HALLUCINATION, VISUAL ( 6 FDA reports)
INFECTION ( 6 FDA reports)
JAUNDICE ( 6 FDA reports)
OXYGEN SATURATION DECREASED ( 6 FDA reports)
PNEUMONIA BACTERIAL ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 6 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 5 FDA reports)
ANOREXIA ( 5 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
BACK PAIN ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
BONE MARROW FAILURE ( 5 FDA reports)
CARDIOMYOPATHY ( 5 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 5 FDA reports)
COLD SWEAT ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
DEEP VEIN THROMBOSIS ( 5 FDA reports)
ENDOSCOPY SMALL INTESTINE ( 5 FDA reports)
ERYTHEMA MULTIFORME ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
LUNG INFILTRATION ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 5 FDA reports)
PRODUCTIVE COUGH ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
RASH GENERALISED ( 5 FDA reports)
SMALL INTESTINE ULCER ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
GASTRIC ULCER ( 4 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 4 FDA reports)
LABORATORY TEST ABNORMAL ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
LUNG ADENOCARCINOMA ( 4 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 4 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 4 FDA reports)
MELAENA ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 4 FDA reports)
PEMPHIGOID ( 4 FDA reports)
PNEUMONITIS ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
PULMONARY MYCOSIS ( 4 FDA reports)
SHOCK ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
TUMOUR LYSIS SYNDROME ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ACUTE RESPIRATORY FAILURE ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 3 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
CANCER PAIN ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CHEST X-RAY ABNORMAL ( 3 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DYSSTASIA ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
ENTEROCOLITIS ( 3 FDA reports)
EOSINOPHIL COUNT INCREASED ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
FRACTURE ( 3 FDA reports)
GENERALISED ERYTHEMA ( 3 FDA reports)
GRANULOMA ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HAEMOLYTIC ANAEMIA ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
LOGORRHOEA ( 3 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 3 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 3 FDA reports)
MIDDLE INSOMNIA ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PULMONARY CONGESTION ( 3 FDA reports)
PULMONARY SARCOIDOSIS ( 3 FDA reports)
PULMONARY TUBERCULOSIS ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
UVEITIS ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ANAL ABSCESS ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANAPHYLACTOID SHOCK ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
ANXIETY DISORDER ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BARIATRIC GASTRIC BALLOON INSERTION ( 2 FDA reports)
BILIRUBINURIA ( 2 FDA reports)
BIOPSY COLON ABNORMAL ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BRONCHITIS CHRONIC ( 2 FDA reports)
CACHEXIA ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CRYING ( 2 FDA reports)
DERMAL CYST ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DUODENAL PERFORATION ( 2 FDA reports)
DUODENAL ULCER ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
ENANTHEMA ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
EYE LUXATION ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
GASTRODUODENAL ULCER ( 2 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 2 FDA reports)
GAZE PALSY ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
IRITIS ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LEUCINE AMINOPEPTIDASE INCREASED ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
MONOCYTE COUNT INCREASED ( 2 FDA reports)
MUCOSAL EROSION ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NEUROGENIC BLADDER ( 2 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OXYGEN SUPPLEMENTATION ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PNEUMOMEDIASTINUM ( 2 FDA reports)
PNEUMORETROPERITONEUM ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
POLYPECTOMY ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RALES ( 2 FDA reports)
RECTAL ULCER ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
REFLUX OESOPHAGITIS ( 2 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TREMOR ( 2 FDA reports)
TRIGEMINAL PALSY ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
WOUND COMPLICATION ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANTI-HBE ANTIBODY POSITIVE ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ASCITES ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
CALCIFICATION OF MUSCLE ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VITREOUS OPACITIES ( 1 FDA reports)

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