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

EYE IRRITATION ( 36 FDA reports)
EYE PAIN ( 16 FDA reports)
VISION BLURRED ( 16 FDA reports)
CONDITION AGGRAVATED ( 13 FDA reports)
LACRIMATION INCREASED ( 11 FDA reports)
DRUG INEFFECTIVE ( 10 FDA reports)
EYE SWELLING ( 10 FDA reports)
EYELID OEDEMA ( 10 FDA reports)
HEADACHE ( 10 FDA reports)
NAUSEA ( 10 FDA reports)
VISUAL IMPAIRMENT ( 10 FDA reports)
CHEST DISCOMFORT ( 9 FDA reports)
ERYTHEMA OF EYELID ( 9 FDA reports)
EYE PRURITUS ( 9 FDA reports)
DERMATITIS CONTACT ( 8 FDA reports)
DRUG HYPERSENSITIVITY ( 8 FDA reports)
DYSPNOEA ( 8 FDA reports)
GLAUCOMA ( 8 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 8 FDA reports)
REACTION TO PRESERVATIVES ( 8 FDA reports)
CHEST PAIN ( 7 FDA reports)
DIPLOPIA ( 7 FDA reports)
EXPIRED DRUG ADMINISTERED ( 7 FDA reports)
OCULAR HYPERAEMIA ( 7 FDA reports)
PHOTOPHOBIA ( 7 FDA reports)
SCLERAL HYPERAEMIA ( 7 FDA reports)
ABNORMAL SENSATION IN EYE ( 6 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 6 FDA reports)
DRY EYE ( 6 FDA reports)
CORONARY ARTERY DISEASE ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
ANXIETY ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
EYELID PTOSIS ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
HALO VISION ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
SINUS CONGESTION ( 4 FDA reports)
THIRST ( 4 FDA reports)
TINNITUS ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
BLINDNESS TRANSIENT ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
PAIN ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PULMONARY CONGESTION ( 3 FDA reports)
RHINORRHOEA ( 3 FDA reports)
ULCERATIVE KERATITIS ( 3 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BURSITIS ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CORNEAL OPACITY ( 2 FDA reports)
CORNEAL PERFORATION ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FALL ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 2 FDA reports)
FRACTURE DISPLACEMENT ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GROIN PAIN ( 2 FDA reports)
HIP ARTHROPLASTY ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INSTILLATION SITE IRRITATION ( 2 FDA reports)
KERATITIS BACTERIAL ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PATHOLOGICAL FRACTURE ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RHINITIS ALLERGIC ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
STRESS FRACTURE ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ANAEMIA POSTOPERATIVE ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
BASE EXCESS DECREASED ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE FORMATION INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BUNDLE BRANCH BLOCK BILATERAL ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COMA ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
DEATH ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE OPERATION ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GRAVITATIONAL OEDEMA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJURY ( 1 FDA reports)
INSTILLATION SITE PAIN ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MESENTERIC ARTERY STENOSIS ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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