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

DRUG ABUSE ( 39 FDA reports)
EYE PAIN ( 33 FDA reports)
CORNEAL EPITHELIUM DEFECT ( 30 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 25 FDA reports)
LACRIMATION INCREASED ( 23 FDA reports)
PHOTOPHOBIA ( 23 FDA reports)
KERATOPATHY ( 18 FDA reports)
HYPOPYON ( 16 FDA reports)
ULCERATIVE KERATITIS ( 15 FDA reports)
CORNEAL OPACITY ( 14 FDA reports)
VISUAL ACUITY REDUCED ( 14 FDA reports)
CORNEAL INFILTRATES ( 11 FDA reports)
CORNEAL OEDEMA ( 10 FDA reports)
POST PROCEDURAL COMPLICATION ( 8 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 8 FDA reports)
CORNEAL EROSION ( 6 FDA reports)
CORNEAL LEUKOMA ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
TOXIC ANTERIOR SEGMENT SYNDROME ( 6 FDA reports)
CHEST PAIN ( 5 FDA reports)
ENDOPHTHALMITIS ( 5 FDA reports)
EYE IRRITATION ( 5 FDA reports)
EYELID OEDEMA ( 5 FDA reports)
ASTHENIA ( 4 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
CORNEAL THINNING ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
OCULAR HYPERAEMIA ( 4 FDA reports)
PAIN ( 4 FDA reports)
ANXIETY ( 3 FDA reports)
CORNEAL PERFORATION ( 3 FDA reports)
CORNEAL SCAR ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
IMPAIRED HEALING ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
PUNCTATE KERATITIS ( 3 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
TREMOR ( 3 FDA reports)
ANAESTHETIC COMPLICATION ( 2 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CORNEAL EPITHELIUM DISORDER ( 2 FDA reports)
CORNEAL NEOVASCULARISATION ( 2 FDA reports)
DERMATITIS CONTACT ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
EXOSTOSIS ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
EYELID FUNCTION DISORDER ( 2 FDA reports)
FACTITIOUS DISORDER ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
IIIRD NERVE INJURY ( 2 FDA reports)
INJURY ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MACULAR SCAR ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NORMAL NEWBORN ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
POST PROCEDURAL PAIN ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALBUMIN URINE ( 1 FDA reports)
AMNIOTIC MEMBRANE GRAFT ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANTERIOR CHAMBER CELL ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
ARCUS LIPOIDES ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ASTIGMATISM ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
ATROPHY OF GLOBE ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLADDER CATHETERISATION ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE SCAN ABNORMAL ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONJUNCTIVAL ABRASION ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORNEAL DEPOSITS ( 1 FDA reports)
CORNEAL ULCER ( 1 FDA reports)
COUGH ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFECTED DERMAL CYST ( 1 FDA reports)
INFECTIOUS CRYSTALLINE KERATOPATHY ( 1 FDA reports)
IRITIS ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KERATITIS VIRAL ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LENS DISLOCATION ( 1 FDA reports)
LIGAMENT SPRAIN ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NODULE ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PHLEBOLITH ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PSEUDOENDOPHTHALMITIS ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RECURRING SKIN BOILS ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
SACROILIITIS ( 1 FDA reports)
SCAR ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPINAL X-RAY ABNORMAL ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
STRESS ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
ULTRASOUND BREAST ABNORMAL ( 1 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VITREOUS PROLAPSE ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WOUND ( 1 FDA reports)
X-RAY LIMB ABNORMAL ( 1 FDA reports)

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