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INTERSTITIAL LUNG DISEASE ( 9 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 8 FDA reports)
PNEUMONIA ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
VOMITING ( 7 FDA reports)
DIZZINESS ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
SEPTIC SHOCK ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
HAEMODIALYSIS ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
MALAISE ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
THIRST ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
ASCITES ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
BLADDER CANCER ( 4 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
PULMONARY MYCOSIS ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
AUTOIMMUNE HEPATITIS ( 3 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
BONE MARROW DEPRESSION ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HAEMOLYTIC ANAEMIA ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
SINUS ARREST ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CALCULUS BLADDER ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
COLITIS COLLAGENOUS ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
EOSINOPHILIC PNEUMONIA ( 2 FDA reports)
FALL ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTROINTESTINAL NECROSIS ( 2 FDA reports)
GINGIVAL HYPERTROPHY ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HYPERACUSIS ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOCOMPLEMENTAEMIA ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
LARGE INTESTINAL ULCER ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LUMBAR SPINAL STENOSIS ( 2 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STENOTROPHOMONAS INFECTION ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VOCAL CORD PARALYSIS ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ANURIA ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIOPSY COLON ABNORMAL ( 1 FDA reports)
BLADDER SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CAROTID ARTERY STENT INSERTION ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
CRYOGLOBULINAEMIA ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDOSCOPY LARGE BOWEL ABNORMAL ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC DILATATION ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTRITIS ATROPHIC ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 1 FDA reports)
GLOMERULONEPHROPATHY ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HELLP SYNDROME ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IGA NEPHROPATHY ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFECTIOUS PERITONITIS ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
KIDNEY RUPTURE ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 1 FDA reports)
MENINGITIS TUBERCULOUS ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL PUSTULE ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PURPURA ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL CYST HAEMORRHAGE ( 1 FDA reports)
RENAL CYST INFECTION ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RHEUMATOID FACTOR INCREASED ( 1 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TRANSPLANT ABSCESS ( 1 FDA reports)
TRAUMATIC HAEMORRHAGE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE CYTOLOGY ABNORMAL ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ACQUIRED ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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