drugs with adverse ocular effects
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Introduction
Includes:
- alpha-1 adrenergic receptor antagonists (alpha-blockers)
- blurred vision
- eye pain
- floppy-iris syndrome (most frequent with tamsulosin)
- amiodarone (Cordarone)
- corneal deposits
- occur in ~70% of patients on amiodarone
- may result in vision loss
- optic neuritis
- optic neuropathy
- optic neuropathy &/or neuritis may occur any time after starting amiodarone (2% of patients on amiodarone) visual impairment & blindness can result
- photosensitivity
- patients taking amiodarone should have a baseline eye exam & eye exams every s6-12 months
- patients should call provider if visual disturbances
- corneal deposits
- bisphosphonates
- blurred vision
- conjunctivitis
- episcleritis
- eye pain
- iritis
- scleritis
- uveitis
- ocular adverse effects are associated with inflammation, possibly immunologic in nature
- may be seen within 48 hours after starting pamidronate
- may be seen two days to 2 weeks after starting alendronate
- stopping bisphosphonate may resolve ocular adverse effects
- canthaxanthin
- altered eye function
- decreased visual acuity
- retinal deposits
- reaction is dose-related
- symptoms are reversible
- patients are frequently asymptomatic
- celecoxib (Celebrex)
- blurred vision
- cataracts
- conjunctivitis
- conjunctival hemorrhage
- eye pain
- glaucoma
- vitreous floaters
- adverse effects might be caused by alteration of retinal blood flow &/or inflammation resulting from secretion of the medication in tears
- stopping celecoxib should resolve most ocular side effects within 72 hours
- chloroquine (Aralen), hydroxychloroquine (Plaquenil)
- blurred vision
- contact lens intolerance
- corneal deposits
- retinopathy
- dose-related, occurs with long-term therapy
- retinal changes & visual disturbances may progress after drug is stopped
- baseline & eye exams every 3-6 months
- discontinue for any visual disturbances
- corticosteroids
- cataracts
- glaucoma
- optic neuritis
- retinopathy
- risk associated with prolonged use of inhaled, oral, or topical corticosteroids
- taper ASAP if intraocular pressure increases
- digoxin
- visual disturbances
- reduced visual acuity
- visual symptoms can occur with therapeutic levels of digoxin
- symptoms can resolve with correction of supratherapeutic levels or with discontinuation of digoxin
- ethambutol (Myambutol, Etibi)
- color vision changes
- optic neuropathy
- may be related to dose and duration of treatment
- generally reversible when ethambutol is stopped
- may continue to progress for 1-2 months after discontinuation
- recovery may be delayed for > 1 year
- irreversible blindness has been reported
- visual field defects
- eye exams at baseline & periodically thereafter
- patients on > 15 mg/kg/day should have monthly eye exams
- notify provider of any vision changes
- isoniazid
- optic neuropathy, usually reversible & less severe than with ethambutol
- isotretinoin (Accutane), vitamin A1
- cataracts
- conjunctivitis
- corneal opacities
- dose-related & resolve in a couple of months after therapy is stopped
- decreased night vision may persist after therapy is stopped
- pseudotumor cerebri (intracranial hypertension)
- papilledema
- photophobia
- reduced tolerance to contact lenses
- visual changes are dose related
- stop retinoid if any visual difficulties or headaches, with eye exam to rule out papilledema secondary to intracranial hypertension
- periodic eye exams if oral retinoid therapy for >= 6 months
- linezolid (Zyvox, Zyvoxam)
- optic neuropathy
- decreased vision & color vision, visual field defects
- reported cases occurred after 5-11 months of therapy
- symptoms improve after discontinuation
- eye exam if treatment for >= 3 months
- optic neuropathy
- niacin (Niaspan)
- cystoid macular edema
- usually resolves within 2 weeks after stopping niacin
- decreased vision
- dry eyes
- cystoid macular edema
- phenothiazines
- cataracts
- dose & drug dependent
- most common with chlorpromazine & thioridazine
- retinopathy
- may develop within weeks-months with high-dose thioridazine
- blurred vision is usually the initial symptom
- cataracts
- phosphodiesterase-5 inhibitors
- blurred vision
- cataracts
- changes in color perception
- conjunctivitis
- dry eyes
- eye hemorrhage
- eye pain
- mydriasis
- non-arteritic anterior ischemic optic neuropathy
- may result in decreased vision or permanent vision loss
- causality of PDE5 inhibitors has not been established
- photophobia
- ocular adverse effects are dose-dependent
- PDE5 inhibitors should not be used in patients with hereditary degenerative retinal disorders
- stop PDE5 inhibitor & call provider if vision loss
- tamoxifen (Nolvadex)
- cataracts, slow blurring of vision
- corneal opacities
- decreased color vision perception
- retinal vein thrombosis
- retinopathy
- commonly occurs after > 1 year of therapy when a total of > 100 gm has been administered
- an acute, reversible retinopathy can also develop within weeks of starting therapy
- patients should have an eye exam at baseline & every 2 years
- call provider for any ocular adverse effects
- telithromycin (Ketek)
- blurred vision
- difficulty focusing
- double vision
- visual adverse events in ~ 2% of patients
- most visual adverse events occur following the 1st or 2nd dose
- visual adverse events may last several hours & recur with subsequent doses in some patients
- symptoms may resolve or continue with continued administration
- women < 40 years are most likely to experience adverse visual events
- call provider for any vision problems
- tiagabine (Gabitril)
- abnormal vision
- deteriorating color vision
- mechanism may be retinal toxicity from elevated levels of GABA
- topiramate (Topamax)
- acute angle-closure glaucoma
- acute myopia, may take weeks to resolve
- increased ocular pressure
- may occur within one month of therapy, & within hours after doubling the dose
- mydriasis
- call provider for blurred vision, visual disturbances, or eye pain
- vigabatrin (Sabril)-Canada only
- optic atrophy
- optic neuritis
- peripheral constriction of visual field
- occurs in ~ 30% of patients
- usually occurs in the first 4 years of treatment
- mechanism may be retinal toxicity from elevated levels of GABA
- visual field defects are likely permanent even after stopping vigabatrin
- visual field examinations before or soon after starting vigabatrin are recommended, then every 3 months thereafter
- voriconazole (Vfend)
- optic neuritis
- papilledema
- ocular adverse effects have occurred mainly in severely ill patients
- if administration > 28 days, visual function should be monitored
More general terms
More specific terms
Additional terms
References
- ↑ Prescriber's Letter 16(1): 2009 Drug-Induced Ocular Effects Detail-Document#: http://prescribersletter.com/(5bhgn1a4ni4cyp2tvybwfh55)/pl/ArticleDD.aspx?li=1&st=1&cs=&s=PRL&pt=3&fpt=25&dd=250124&pb=PRL (subscription needed) http://www.prescribersletter.com