Lotepred DS Ophthalmic Suspension

Loteprednol Etabonate Eye prep
1%
Aristopharma Limited
Pack size 5 ml drop
Unite Price 230.00 BDT

Indications

Lotepred DS Ophthalmic Suspension is used for: Postoperative ocular inflammation and pain, Allergic conjunctivitis, Ocular inflammation

Adult Dose

Ophthalmic Postoperative ocular inflammation and pain Indicated for treatment of postoperative inflammation and pain following ocular surgery (1% preparation) Instill 1-2 drops into affected eye(s) BID beginning the day after surgery and continuing throughout the first 2 weeks postoperatively (0.5% preparation) Gel or suspension: Apply 1-2 drops into conjunctival sac of affected eye(s) QID beginning the day after surgery and continuing throughout the first 2 weeks postoperatively Ointment: Apply ~0.5 inch ribbon into conjunctival sac(s) QID beginning the day after surgery and continuing throughout the first 2 weeks postoperatively Seasonal Allergic Conjunctivitis Indicated for temporary relief of signs and symptoms of seasonal allergic conjunctivitis (0.2% preparation) Instill 1 drop into affected eye(s) QID Steroid Responsive Inflammatory Conditions Indicated for steroid responsive inflammatory conditions of the palpebral and bulbar conjunctiva, cornea and anterior segment of the globe (eg, allergic conjunctivitis, acne rosacea, superficial punctate keratitis, herpes zoster keratitis, iritis, cyclitis, selected infective conjunctivitides) when steroid use is accepted to obtain an advisable diminution in edema and inflammation (0.5% preparation) Suspension only Apply 1-2 drops into the conjunctival sac of affected eye(s) QID During initial treatment within the first week, may increase dose up to 1 drop q1hr, if necessary Do not to discontinue therapy prematurely; if signs and symptoms fail to improve after 2 days, re-evaluate patient

Child Dose

Postoperative Inflammation Indicated for treatment of postoperative inflammation and pain following ocular surgery (0.5% preparation) Gel or suspension: Apply 1-2 drops into conjunctival sac of affected eye(s) QID beginning the day after surgery and continuing throughout the first 2 weeks postoperatively Ointment: Apply ~0.5 inch ribbon into conjunctival sac(s) QID beginning the day after surgery and continuing throughout the first 2 weeks postoperatively Steroid Responsive Inflammatory Conditions Indicated for steroid responsive inflammatory conditions of the palpebral and bulbar conjunctiva, cornea and anterior segment of the globe (eg, allergic conjunctivitis, acne rosacea, superficial punctate keratitis, herpes zoster keratitis, iritis, cyclitis, selected infective conjunctivitides) when steroid use is accepted to obtain an advisable diminution in edema and inflammation (0.5% preparation) Suspension only Apply 1-2 drops into the conjunctival sac of affected eye(s) QID During initial treatment within the first week, may increase dose up to 1 drop q1hr, if necessary Do not to discontinue therapy prematurely; if signs and symptoms fail to improve after 2 days, re-evaluate patient

Renal Dose

Administration

Contra Indications

Contraindicated in individuals with known or suspected hypersensitivity to any of the ingredients of this preparation and to other corticosteroids. Viral infections of the cornea and conjunctiva; mycobacterial eye infection; fungal infections of ocular structures. Contraindicated in most viral diseases of the cornea and conjunctiva including epithelial herpes simplex keratitis (dendritic keratitis), vaccinia and varicella, and also in mycobacterial infection of the eye and fungal diseases of ocular structures. Contraindicated in individuals with known or suspected hypersensitivity to any of the ingredients of this preparation and to other corticosteroids.

Precautions

May mask and exacerbate existing ocular infection. Re-evaluate patients if symptoms do not improve after 2 days. Glaucoma; may delay healing after cataract surgery. Monitor intraocular pressure (prolonged use).

Pregnancy-Lactation

Pregnancy (0.1% preparation) Drug is not absorbed systemically following topical ophthalmic administration and maternal use is not expected to result in fetal exposure to drug (0.5% preparation) There are no adequate and well controlled studies in pregnant women; use during pregnancy only if the potential benefit justifies the potential risk to the fetus Lactation (0.1% preparation) Drug is not absorbed systemically by the mother following topical ophthalmic administration, and breastfeeding is not expected to result in exposure of the child (0.5% and 0.2% preparation) There are no data on presence of loteprednol etabonate in human milk, effects on breastfed infant, or on milk production; developmental and health benefits of breastfeeding should be considered, along with mother’s clinical need for therapy and any potential adverse effects on breastfed infant It is not known whether topical ophthalmic administration of corticosteroids could result in sufficient systemic absorption to produce detectable quantities in human milk Systemic steroids appear in human milk and could suppress growth, interfere with endogenous corticosteroid production, or cause other untoward effects

Interactions

Side Effects

Side effects of Loteprednol Etabonate Eye prep : >10% (0.5% ointment only) Anterior chamber inflammation (~25%) 5-15% (0.5% suspension only) Abnormal vision/blurring Burning on instillation Chemosis Discharge Dry eyes Epiphora Foreign body sensation Itching Photophobia <5% (0.5% gel only) Anterior chamber inflammation (5%) Eye pain (2%) Foreign body sensation (2%) (0.5% suspension only) Conjunctivitis Corneal abnormalities Eyelid erythema Keratoconjunctivitis Ocular irritation/pain/discomfort Papillae Uveitis (0.5% ointment only) Conjunctival hyperemia (4-5%) Corneal edema (4-5%) Eye pain (4-5%) Headache (1.5%) Frequency Not Defined (0.1% only) Infrequent optic nerve damage Visual acuity and field defects Posterior subcapsular cataract formation Delayed wound healing Secondary ocular infection from pathogens (eg, herpes simplex) Perforation of the globe where there is thinning of the cornea or sclera

Mode of Action

Loteprednol is a synthetic nonfluorinated glucocorticoid. It stimulates the production of lipicortins, proteins that modulate the activity of prostaglandins and leukotrienes.

Note

Lotepred DS 1% Ophthalmic Suspension generic name is Loteprednol Etabonate Eye prep. Lotepred DS 1% Ophthalmic Suspension is manufactured by Aristopharma LimitedLotepred DS is availble in all over Bangladesh. Mes BD drug index information on Lotepred DS Ophthalmic Suspension is not intended for diagnosis, medical advice or treatment; neither intended to be a substitute for the exercise of professional judgment.

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