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

DIARRHOEA ( 49 FDA reports)
PYREXIA ( 40 FDA reports)
PLATELET COUNT DECREASED ( 35 FDA reports)
CONDITION AGGRAVATED ( 33 FDA reports)
PNEUMONIA ( 33 FDA reports)
HYPOAESTHESIA ( 27 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 25 FDA reports)
MALAISE ( 23 FDA reports)
INTERSTITIAL LUNG DISEASE ( 22 FDA reports)
ANOREXIA ( 21 FDA reports)
CONSTIPATION ( 21 FDA reports)
RENAL IMPAIRMENT ( 21 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 21 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 20 FDA reports)
PLEURAL EFFUSION ( 20 FDA reports)
BLOOD ALBUMIN DECREASED ( 19 FDA reports)
FALL ( 19 FDA reports)
NEUROPATHY PERIPHERAL ( 17 FDA reports)
URINARY TRACT INFECTION ( 17 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 16 FDA reports)
HYPOKALAEMIA ( 16 FDA reports)
RASH ( 16 FDA reports)
BLOOD PRESSURE DECREASED ( 15 FDA reports)
PAIN ( 15 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 14 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 14 FDA reports)
DRUG HYPERSENSITIVITY ( 14 FDA reports)
HEADACHE ( 14 FDA reports)
LOSS OF CONSCIOUSNESS ( 14 FDA reports)
SHOCK ( 14 FDA reports)
ANAEMIA ( 13 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 13 FDA reports)
DECREASED APPETITE ( 13 FDA reports)
DISEASE PROGRESSION ( 13 FDA reports)
VISUAL ACUITY REDUCED ( 13 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 12 FDA reports)
ARTHRALGIA ( 12 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 12 FDA reports)
EOSINOPHIL COUNT INCREASED ( 12 FDA reports)
NAUSEA ( 12 FDA reports)
PANCYTOPENIA ( 12 FDA reports)
SOMNOLENCE ( 12 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 12 FDA reports)
BLOOD POTASSIUM DECREASED ( 11 FDA reports)
CONVULSION ( 11 FDA reports)
GAIT DISTURBANCE ( 11 FDA reports)
HAEMOGLOBIN DECREASED ( 11 FDA reports)
NASOPHARYNGITIS ( 11 FDA reports)
OSTEOMYELITIS ( 11 FDA reports)
RESPIRATORY FAILURE ( 11 FDA reports)
SEPSIS ( 11 FDA reports)
VOMITING ( 11 FDA reports)
DEHYDRATION ( 10 FDA reports)
DYSPNOEA ( 10 FDA reports)
HYPERTENSION ( 10 FDA reports)
ABDOMINAL PAIN ( 9 FDA reports)
BLOOD UREA INCREASED ( 9 FDA reports)
DIZZINESS ( 9 FDA reports)
LIVER DISORDER ( 9 FDA reports)
NEUTROPHIL COUNT DECREASED ( 9 FDA reports)
OSTEONECROSIS ( 9 FDA reports)
PULMONARY EMBOLISM ( 9 FDA reports)
SYNCOPE ( 9 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 8 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
HERPES ZOSTER ( 8 FDA reports)
INFECTION ( 8 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 8 FDA reports)
PAROTITIS ( 8 FDA reports)
PNEUMONIA BACTERIAL ( 8 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 8 FDA reports)
STERNAL FRACTURE ( 8 FDA reports)
TREMOR ( 8 FDA reports)
URINARY RETENTION ( 8 FDA reports)
BLOOD BILIRUBIN INCREASED ( 7 FDA reports)
BONE PAIN ( 7 FDA reports)
CARDIAC FAILURE ( 7 FDA reports)
DEEP VEIN THROMBOSIS ( 7 FDA reports)
DRUG INTERACTION ( 7 FDA reports)
HAEMATOCRIT DECREASED ( 7 FDA reports)
HYPOCALCAEMIA ( 7 FDA reports)
HYPONATRAEMIA ( 7 FDA reports)
NEUROGENIC BLADDER ( 7 FDA reports)
NO THERAPEUTIC RESPONSE ( 7 FDA reports)
ORTHOSTATIC HYPOTENSION ( 7 FDA reports)
PROTEIN TOTAL DECREASED ( 7 FDA reports)
PSEUDARTHROSIS ( 7 FDA reports)
RENAL FAILURE ( 7 FDA reports)
RENAL FAILURE ACUTE ( 7 FDA reports)
TRANSPLANT REJECTION ( 7 FDA reports)
URTICARIA ( 7 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 7 FDA reports)
AGRANULOCYTOSIS ( 6 FDA reports)
ASTHENIA ( 6 FDA reports)
BLINDNESS UNILATERAL ( 6 FDA reports)
BLOOD CALCIUM DECREASED ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 6 FDA reports)
BRONCHIECTASIS ( 6 FDA reports)
BRONCHITIS ( 6 FDA reports)
CEREBRAL INFARCTION ( 6 FDA reports)
CHOLECYSTITIS ( 6 FDA reports)
CYSTITIS ( 6 FDA reports)
GASTRITIS ( 6 FDA reports)
HEPATITIS B ( 6 FDA reports)
HYPOPHAGIA ( 6 FDA reports)
MELAENA ( 6 FDA reports)
MOVEMENT DISORDER ( 6 FDA reports)
MULTI-ORGAN FAILURE ( 6 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 6 FDA reports)
RESPIRATORY ARREST ( 6 FDA reports)
STAPHYLOCOCCAL INFECTION ( 6 FDA reports)
ASTHMA ( 5 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 5 FDA reports)
BONE MARROW DEPRESSION ( 5 FDA reports)
COUGH ( 5 FDA reports)
DRUG ERUPTION ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
DYSGEUSIA ( 5 FDA reports)
FACE OEDEMA ( 5 FDA reports)
FEELING ABNORMAL ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
GLAUCOMA ( 5 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 5 FDA reports)
HAEMODIALYSIS ( 5 FDA reports)
HEARING IMPAIRED ( 5 FDA reports)
HEMIPLEGIA ( 5 FDA reports)
HYPERGLYCAEMIA ( 5 FDA reports)
IMMUNOSUPPRESSION ( 5 FDA reports)
LABORATORY TEST ABNORMAL ( 5 FDA reports)
LEUKOPENIA ( 5 FDA reports)
LUNG INFECTION ( 5 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 5 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 5 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 5 FDA reports)
MENINGITIS TUBERCULOUS ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
OPPORTUNISTIC INFECTION ( 5 FDA reports)
OSTEOPOROSIS ( 5 FDA reports)
PERICARDIAL EFFUSION ( 5 FDA reports)
PHARYNGEAL OEDEMA ( 5 FDA reports)
PNEUMOTHORAX ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
RENAL DISORDER ( 5 FDA reports)
RESPIRATORY DISORDER ( 5 FDA reports)
SPINAL COMPRESSION FRACTURE ( 5 FDA reports)
STEVENS-JOHNSON SYNDROME ( 5 FDA reports)
TETANY ( 5 FDA reports)
TINNITUS ( 5 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
VIRAL INFECTION ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 4 FDA reports)
ACETONAEMIC VOMITING ( 4 FDA reports)
ACUTE DISSEMINATED ENCEPHALOMYELITIS ( 4 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
ANAPHYLACTOID REACTION ( 4 FDA reports)
ANTIBODY TEST POSITIVE ( 4 FDA reports)
ASPERGILLOSIS ( 4 FDA reports)
BACTERIAL INFECTION ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
BLOOD SODIUM INCREASED ( 4 FDA reports)
BRONCHOPNEUMONIA ( 4 FDA reports)
CATHETER RELATED INFECTION ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
DEVICE RELATED INFECTION ( 4 FDA reports)
DISEASE RECURRENCE ( 4 FDA reports)
ELECTROLYTE IMBALANCE ( 4 FDA reports)
EYE SWELLING ( 4 FDA reports)
FEMORAL NECK FRACTURE ( 4 FDA reports)
FEMUR FRACTURE ( 4 FDA reports)
GASTRITIS EROSIVE ( 4 FDA reports)
GRANULOCYTOPENIA ( 4 FDA reports)
HEART RATE DECREASED ( 4 FDA reports)
HYPERCALCAEMIA ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPERLIPIDAEMIA ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
INFLUENZA ( 4 FDA reports)
LUPUS NEPHRITIS ( 4 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 4 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 4 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
NEPHROTIC SYNDROME ( 4 FDA reports)
ORAL INTAKE REDUCED ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
PHARYNGITIS ( 4 FDA reports)
PLEURISY ( 4 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 4 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 4 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 4 FDA reports)
PURPURA ( 4 FDA reports)
RASH PAPULAR ( 4 FDA reports)
SICK SINUS SYNDROME ( 4 FDA reports)
THIRST ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
TONIC CONVULSION ( 4 FDA reports)
TORSADE DE POINTES ( 4 FDA reports)
TRANSPLANT ( 4 FDA reports)
TREATMENT NONCOMPLIANCE ( 4 FDA reports)
VARICELLA ( 4 FDA reports)
VASCULITIS ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ABNORMAL SENSATION IN EYE ( 3 FDA reports)
ABORTION INDUCED ( 3 FDA reports)
APHTHOUS STOMATITIS ( 3 FDA reports)
ARTERIOVENOUS MALFORMATION ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD CULTURE POSITIVE ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BODY TEMPERATURE DECREASED ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CARDIAC FAILURE ACUTE ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
CLOSTRIDIUM COLITIS ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
COLONIC POLYP ( 3 FDA reports)
DEATH ( 3 FDA reports)
DYSSTASIA ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
ENTEROCOCCAL INFECTION ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
EPIGASTRIC DISCOMFORT ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
FUNGAL SEPSIS ( 3 FDA reports)
GASTRIC ULCER ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 3 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPOPHOSPHATAEMIA ( 3 FDA reports)
IMMUNE SYSTEM DISORDER ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
INTESTINAL ISCHAEMIA ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
JAW DISORDER ( 3 FDA reports)
LUMBAR SPINAL STENOSIS ( 3 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 3 FDA reports)
LUNG ADENOCARCINOMA ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 3 FDA reports)
MOUTH HAEMORRHAGE ( 3 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NEPHROGENIC ANAEMIA ( 3 FDA reports)
NOCARDIOSIS ( 3 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 3 FDA reports)
OPTIC NERVE DISORDER ( 3 FDA reports)
OSTEOSCLEROSIS ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
PLATELET COUNT INCREASED ( 3 FDA reports)
PO2 DECREASED ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
PRIMARY SEQUESTRUM ( 3 FDA reports)
PROTEIN URINE PRESENT ( 3 FDA reports)
PSEUDOMONAS INFECTION ( 3 FDA reports)
PULMONARY FIBROSIS ( 3 FDA reports)
PULMONARY MYCOSIS ( 3 FDA reports)
PYELONEPHRITIS ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SCEDOSPORIUM INFECTION ( 3 FDA reports)
STRESS FRACTURE ( 3 FDA reports)
STRESS ULCER ( 3 FDA reports)
THROMBOPHLEBITIS ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABSCESS INTESTINAL ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ADRENAL ATROPHY ( 2 FDA reports)
ADRENAL INSUFFICIENCY ( 2 FDA reports)
ANOREXIA NERVOSA ( 2 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASPERGER'S DISORDER ( 2 FDA reports)
ASPERGILLUS TEST POSITIVE ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ASTHENOPIA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
ATRIAL THROMBOSIS ( 2 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 2 FDA reports)
BILIARY TRACT INFECTION ( 2 FDA reports)
BLOOD CALCIUM INCREASED ( 2 FDA reports)
BLOOD CREATININE DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 2 FDA reports)
BLOOD IRON DECREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CATHETER SITE HAEMORRHAGE ( 2 FDA reports)
CEREBELLAR SYNDROME ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 2 FDA reports)
COLITIS MICROSCOPIC ( 2 FDA reports)
COLOUR BLINDNESS ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 2 FDA reports)
CREPITATIONS ( 2 FDA reports)
CROHN'S DISEASE ( 2 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEMYELINATION ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSPHORIA ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM R ON T PHENOMENON ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
EXANTHEM ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 2 FDA reports)
FOREIGN BODY TRAUMA ( 2 FDA reports)
GASTRIC CANCER ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GINGIVAL ATROPHY ( 2 FDA reports)
GLOMERULONEPHRITIS FOCAL ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HEPATORENAL SYNDROME ( 2 FDA reports)
HYPERAMYLASAEMIA ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
ILEUS ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INJURY ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
INTRACARDIAC THROMBUS ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
JOINT CONTRACTURE ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
LACERATION ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LUNG TRANSPLANT REJECTION ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
MENINGITIS ASEPTIC ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MONOCYTE COUNT INCREASED ( 2 FDA reports)
MOUTH BREATHING ( 2 FDA reports)
MUCOSAL HAEMORRHAGE ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
NEOPLASM PROGRESSION ( 2 FDA reports)
NEPHROSCLEROSIS ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
NON-CARDIOGENIC PULMONARY OEDEMA ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PARONYCHIA ( 2 FDA reports)
PEMPHIGOID ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PERITONEAL DIALYSIS ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PERITONITIS BACTERIAL ( 2 FDA reports)
PITUITARY TUMOUR BENIGN ( 2 FDA reports)
PLANTAR FASCIITIS ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POST HERPETIC NEURALGIA ( 2 FDA reports)
PROTEIN TOTAL INCREASED ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PURULENT DISCHARGE ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 2 FDA reports)
RENAL ATROPHY ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RETINAL VEIN OCCLUSION ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
SALIVARY GLAND PAIN ( 2 FDA reports)
SCOLIOSIS ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SUPERINFECTION ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
THROMBOTIC STROKE ( 2 FDA reports)
THYMECTOMY ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
THYROID NEOPLASM ( 2 FDA reports)
TOOTH FRACTURE ( 2 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 2 FDA reports)
URINARY OCCULT BLOOD POSITIVE ( 2 FDA reports)
VENOUS STASIS ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VIRAL PERICARDITIS ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
XEROSIS ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
AMYLOIDOSIS ( 1 FDA reports)
ANAEMIA FOLATE DEFICIENCY ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANTI-HBC IGG ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
ATYPICAL FEMUR FRACTURE ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BASOPHIL COUNT DECREASED ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BLADDER DIVERTICULUM ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALUMINIUM INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 1 FDA reports)
BLOOD CORTISOL ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIAC VALVE VEGETATION ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL VASOCONSTRICTION ( 1 FDA reports)
CEREBROVASCULAR ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
CEREBROVASCULAR SPASM ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLLAGEN DISORDER ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CRYOGLOBULINAEMIA ( 1 FDA reports)
CSF CELL COUNT INCREASED ( 1 FDA reports)
CSF PROTEIN ABNORMAL ( 1 FDA reports)
CYCLIC VOMITING SYNDROME ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DIVERTICULUM GASTRIC ( 1 FDA reports)
DNA ANTIBODY POSITIVE ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ECHINOCOCCIASIS ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
EXPOSED BONE IN JAW ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FRACTURE DISPLACEMENT ( 1 FDA reports)
FUNGAL ENDOCARDITIS ( 1 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC ULCER HELICOBACTER ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 1 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEAD LAG ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HELLP SYNDROME ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HOMANS' SIGN ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HORSESHOE KIDNEY ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOCOMPLEMENTAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
ICHTHYOSIS ACQUIRED ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMMUNOGLOBULINS INCREASED ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFECTION MASKED ( 1 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERLEUKIN LEVEL INCREASED ( 1 FDA reports)
INTESTINAL POLYPECTOMY ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
JUVENILE ARTHRITIS ( 1 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LUNG TRANSPLANT ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
MENINGITIS LISTERIA ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MILIARY PNEUMONIA ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEITIS ( 1 FDA reports)
OSTEOMYELITIS ACUTE ( 1 FDA reports)
OVARIAN GERM CELL TERATOMA BENIGN ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHYTOTHERAPY ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMOCYSTIS TEST POSITIVE ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
POOR PERSONAL HYGIENE ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROTEIN ALBUMIN RATIO DECREASED ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 1 FDA reports)
PULMONARY BULLA ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
RALES ( 1 FDA reports)
RENAL ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RETROPERITONEAL ABSCESS ( 1 FDA reports)
RHEUMATOID FACTOR INCREASED ( 1 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SHUNT ANEURYSM ( 1 FDA reports)
SHUNT OCCLUSION ( 1 FDA reports)
SHUNT THROMBOSIS ( 1 FDA reports)
SILICOSIS ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
SPUTUM PURULENT ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STREPTOCOCCAL SEROLOGY ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TACHYPHYLAXIS ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THYMOMA ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TOOTH INJURY ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
ULCER ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
UROBILIN URINE PRESENT ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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