Latanoprost ophthalmic Side Effects
Not all side effects for latanoprost ophthalmic may be reported. You should always consult a doctor or healthcare professional for medical advice. Side effects can be reported to the FDA here.
For the Consumer
Applies to latanoprost ophthalmic: ophthalmic solution
In addition to its needed effects, some unwanted effects may be caused by latanoprost ophthalmic. In the event that any of these side effects do occur, they may require medical attention.
You should check with your doctor immediately if any of these side effects occur when taking latanoprost ophthalmic:Less common
- Eyelid crusting, redness, swelling, discomfort, or pain
- difficulty breathing
- noisy breathing
- redness of eye or inside of eyelid
- shortness of breath
- swelling of the eye
- tightness in chest
If any of the following side effects occur while taking latanoprost ophthalmic, check with your doctor or nurse as soon as possible:More common
- Blurred vision, eye irritation, or tearing
- darkening of eyelid skin color
- increase in brown color in colored part of eye
- longer, thicker, and darker eyelashes
- Angina pectoris or other chest pain
- cold or flu symptoms
- eye pain
- pain in muscles, joints, or back
- skin rash
- Discharge from the eye
- double vision or other change in vision
- sensitivity of eye to light
- sore throat
Some of the side effects that can occur with latanoprost ophthalmic may not need medical attention. As your body adjusts to the medicine during treatment these side effects may go away. Your health care professional may also be able to tell you about ways to reduce or prevent some of these side effects. If any of the following side effects continue, are bothersome or if you have any questions about them, check with your health care professional:More common
- Burning of eye
- feeling of something in eye
- itching of eye
- stinging of eye
- Dryness of eye
For Healthcare Professionals
Applies to latanoprost ophthalmic: ophthalmic solution
Ocular side effects have been reported the most frequently. These have included blurred vision, burning and stinging, conjunctival hyperemia, foreign body sensation, itching, increased pigmentation of the iris, and punctate epithelial keratopathy in 5% to 15% of patients. Dry eye, excessive tearing, eye pain, lid crusting, lid discomfort/pain, lid edema, lid erythema and photophobia have been observed in 1% to 4% of patients. Conjunctivitis, diplopia and discharge from the eye have been reported in less than 1% of patients. Retinal artery embolus, retinal detachment, and vitreous hemorrhage from diabetic retinopathy have been reported rarely. Choroidal detachment, hypotony, macular edema (including cystoid macular edema), pigmented iris cysts, corneal edema, corneal erosions, keratitis, and herpes keratitis have also been reported. Paradoxical increases in intraocular pressure (IOP) and recurrence of uveal inflammation have been reported in patients with uveitic glaucoma. Periorbital and lid changes resulting in deepening of the eyelid sulcus have also been reported.[Ref]
Latanoprost can increase the amount of brown pigment in the eye by stimulating melanin production in melanocytes. The change in eye color occurs gradually over months to years and may be permanent. The entire or parts of the iris may be affected. Changes may be more prominent in patients with green- brown, blue/gray- brown or yellow- brown irides.
Conjunctival hyperemia is generally most pronounced during the start of therapy and may subside following prolonged use. In clinical trials, the hyperemia tended to be mild or moderate and rarely resulted in withdrawal from therapy.
A 6- month multicenter, randomized, investigator- masked study (n=136) of patients receiving daily latanoprost therapy reported conjunctival hyperemia in up to 42.5% of patients and a single case of anterior uveitis requiring treatment with topical corticosteroids. The mean grade of hyperemia was 0.28 on a scale of 1 to 3.
An open-label, multinational, multicenter, uncontrolled study of latanoprost administered daily for up to 5 years reported an increase in iris pigmentation in one-third of patients. This effect was generally reported within the first 36 months of therapy in patients with nonhomogenous eye color. There appeared to be no effect on the efficacy or overall safety of latanoprost.[Ref]
Respiratory side effects have included upper respiratory infections in 4% of patients. Asthma, exacerbation of asthma, and dyspnea have also been reported.[Ref]
Musculoskeletal side effects have included arthralgias and myalgias (usually back pain) in 1% to 2% of patients.[Ref]
Cardiovascular side effects have rarely included chest pain and angina pectoris (1% to 2%).[Ref]
Hypersensitivity reactions have included rash or skin problems in 1% to 2% of patients.[Ref]
The manufacturer reports eyelash changes are usually reversible following discontinuation of therapy.
Four cases of poliosis have been reported in as early as 6 weeks of treatment. The affected lashes were interspersed with normally pigmented lashes. Hypertrichosis was also reported in 2 of the 4 patients.
A 6- month, multicenter, randomized, investigator- masked study (n=136) reported a single case of eyelash growth with daily latanoprost therapy.
A 61- year- old man reported his upper eyelashes had been obscuring his vision for approximately 2 months after instilling latanoprost daily to both eyes for approximately a 2- year duration. Further examination revealed bilateral trichomegaly with potentially irreversible lash ptosis.[Ref]
Dermatologic side effects have rarely included reversible hyperpigmentation of the eyelids, eyelashes, periocular area, temporal area, neck, and back. Increase in length, thickness, and number of eyelashes and/or vellus hairs, changes in the direction of the growth of eyelashes, poliosis, contact dermatitis, and toxic epidermal necrolysis have also been reported. One case of lash ptosis has been reported.[Ref]
Nervous system side effects have included postmarketing reports of dizziness and headache.[Ref]
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20. Chen CS, Wells J, Craig JE "Topical prostaglandin F(2alpha) analog induced poliosis." Am J Ophthalmol 137 (2004): 965-6
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