ULCERATIVE KERATITIS | 12 |
Cystoid macular oedema | 11 |
Eye irritation | 9 |
Eye pain | 7 |
CORNEAL PERFORATION | 6 |
Product use in unapproved indication | 5 |
Off label use | 5 |
Intentional product use issue | 5 |
Treatment failure | 4 |
Swelling of eyelid | 4 |
Pruritus | 4 |
Product packaging quantity issue | 4 |
MENTAL STATUS CHANGES | 4 |
JAUNDICE | 4 |
Drug ineffective | 4 |
Drug dose omission | 4 |
Dermatitis allergic | 4 |
COAGULOPATHY | 4 |
Blepharitis | 4 |
ABDOMINAL PAIN | 4 |
Visual impairment | 3 |
Punctate keratitis | 3 |
Ocular discomfort | 3 |
NAUSEA | 3 |
Macular oedema | 3 |
CORNEAL DISORDER | 3 |
WOUND SECRETION | 2 |
VOMITING | 2 |
VISUAL ACUITY REDUCED | 2 |
Vision blurred | 2 |
TREATMENT NONCOMPLIANCE | 2 |
Product quality issue | 2 |
Product physical consistency issue | 2 |
Product colour issue | 2 |
Ocular hyperaemia | 2 |
Mydriasis | 2 |
Medication residue present | 2 |
LIVER TRANSPLANT | 2 |
Keratitis | 2 |
Halo vision | 2 |
FATIGUE | 2 |
ENDOPHTHALMITIS | 2 |
Drug ineffective for unapproved indication | 2 |
Drug hypersensitivity | 2 |
Drug administration error | 2 |
CORNEAL SCAR | 2 |
Corneal opacity | 2 |
CORNEAL OEDEMA | 2 |
Corneal erosion | 2 |
CONDITION AGGRAVATED | 2 |
CATARACT | 2 |
Visual field defect | 1 |
TRANSPLANT | 1 |
Toxic epidermal necrolysis | 1 |
Toxic anterior segment syndrome | 1 |
Tooth discolouration | 1 |
Seizure | 1 |
SCLERAL THINNING | 1 |
SCLERAL GRAFT | 1 |
SCLERAL DISORDER | 1 |
Scleral discolouration | 1 |
Retinal haemorrhage | 1 |
Retinal detachment | 1 |
Retinal artery occlusion | 1 |
Rash | 1 |
PYREXIA | 1 |
Product supply issue | 1 |
Product prescribing error | 1 |
Product label issue | 1 |
Product dropper issue | 1 |
Product dose omission issue | 1 |
Product container issue | 1 |
Posterior capsule opacification | 1 |
Photosensitivity reaction | 1 |
Photophobia | 1 |
Periorbital swelling | 1 |
Pain | 1 |
Overdose | 1 |
Ocular pemphigoid | 1 |
Night blindness | 1 |
MOUTH BREATHING | 1 |
Migraine | 1 |
Metamorphopsia | 1 |
MALAISE | 1 |
MACULOPATHY | 1 |
MACULAR DEGENERATION | 1 |
Loss of consciousness | 1 |
Lacrimation increased | 1 |
Iritis | 1 |
Iris adhesions | 1 |
Intraocular pressure increased | 1 |
Instillation site pain | 1 |
Instillation site irritation | 1 |
Instillation site haemorrhage | 1 |
Instillation site dryness | 1 |
Incorrect dose administered | 1 |
IMPAIRED HEALING | 1 |
IMPAIRED DRIVING ABILITY | 1 |
Hyperaemia | 1 |
HEADACHE | 1 |
GRAFT COMPLICATION | 1 |
Face oedema | 1 |
Eyelid oedema | 1 |
Eye inflammation | 1 |
Eye infection | 1 |
Eye disorder | 1 |
Expired product administered | 1 |
Erythema | 1 |
Epistaxis | 1 |
Ear pain | 1 |
DYSPNOEA | 1 |
Dry eye | 1 |
Drug prescribing error | 1 |
Drug interaction | 1 |
Diplopia | 1 |
DETACHED DESCEMET'S MEMBRANE | 1 |
Cytomegalovirus infection | 1 |
Corneal transplant | 1 |
CORNEAL THINNING | 1 |
Corneal operation | 1 |
CORNEAL INFECTION | 1 |
CORNEAL EPITHELIUM DEFECT | 1 |
CONSTIPATION | 1 |
Conjunctivitis | 1 |
Conjunctival oedema | 1 |
CATARACT OPERATION COMPLICATION | 1 |
CATARACT OPERATION | 1 |
CARDIAC ASTHMA | 1 |
CARDIAC ARREST | 1 |
Burning sensation | 1 |
Blindness | 1 |
ASTHMA | 1 |
ARTHRALGIA | 1 |
Anterior chamber inflammation | 1 |
Anterior chamber disorder | 1 |
Anterior chamber cell | 1 |
ANAPHYLACTIC REACTION | 1 |
AMNIOTIC MEMBRANE GRAFT | 1 |
Accidental exposure to product | 1 |
ABDOMINAL PAIN LOWER | 1 |