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

EYE PAIN ( 16 FDA reports)
EYE IRRITATION ( 14 FDA reports)
IMPAIRED HEALING ( 8 FDA reports)
ULCERATIVE KERATITIS ( 8 FDA reports)
EPISTAXIS ( 7 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 6 FDA reports)
CEREBROVASCULAR ACCIDENT ( 6 FDA reports)
OVERDOSE ( 5 FDA reports)
VISION BLURRED ( 5 FDA reports)
SENSATION OF FOREIGN BODY ( 4 FDA reports)
CHEMICAL EYE INJURY ( 4 FDA reports)
CORNEAL EPITHELIUM DEFECT ( 4 FDA reports)
PHARYNGEAL ERYTHEMA ( 4 FDA reports)
GLOSSITIS ( 4 FDA reports)
CORNEAL OPACITY ( 4 FDA reports)
OCULAR HYPERAEMIA ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
DEATH ( 3 FDA reports)
MACULAR OEDEMA ( 3 FDA reports)
LACRIMATION INCREASED ( 3 FDA reports)
SUPERFICIAL INJURY OF EYE ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CORNEAL DISORDER ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
DIFFUSE LAMELLAR KERATITIS ( 2 FDA reports)
OCULAR DISCOMFORT ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
HAEMORRHAGIC STROKE ( 2 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 2 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFUSION SITE HAEMORRHAGE ( 1 FDA reports)
INSTILLATION SITE PAIN ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
INTRAOCULAR PRESSURE TEST ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
DRUG LABEL CONFUSION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OPHTHALMOPLEGIC MIGRAINE ( 1 FDA reports)
CORNEAL OEDEMA ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
CORNEAL INFILTRATES ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
CATARACT ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)

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