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    Default Pilocarpine Eye Drops

    Indications and Usage for Pilocarpine Eye Drops
    Pilocarpine Hydrochloride Ophthalmic Solution is indicated for the:
    Reduction of Elevated Intraocular Pressure (IOP) in Patients with Open-Angle Glaucoma or Ocular Hypertension

    Management of Acute Angle-Closure Glaucoma

    Prevention of Postoperative Elevated IOP Associated with Laser Surgery

    Induction of Miosis

    Pilocarpine Drops attachment.php?attachmentid=328&stc=1&d=1435863503
    Pilocarpine Eye Drops Dosage and Administration
    Reduction of Elevated Intraocular Pressure (IOP) in Patients with Open-Angle Glaucoma or Ocular Hypertension
    One drop of Pilocarpine Hydrochloride Ophthalmic Solution 1%, 2% or 4% should be applied topically in the eye(s) up to four times daily.
    Pilocarpine-naïve patients should be started on the 1% concentration as higher concentrations are often not tolerated initially. The frequency of instillation and concentration of Pilocarpine Hydrochloride Ophthalmic Solution are determined by the severity of the elevated intraocular pressure and miotic response of the patient. To limit systemic exposure to pilocarpine, patients may be instructed to perform punctal occlusion for 2 minutes after instillation of Pilocarpine Hydrochloride Ophthalmic Solution.

    Management of Acute Angle-Closure Glaucoma
    Prior to Pilocarpine Hydrochloride Ophthalmic Solution use, treatment with secretory suppressants and hyperosmotic agents may be needed to lower IOP below 50 mmHg and relieve iris ischemia.
    For initial management of acute angle-closure glaucoma, one drop of Pilocarpine Hydrochloride Ophthalmic Solution 1% or 2% may be applied topically in the eye(s) up to three times over a 30-minute period.
    If laser iridoplasty or iridomy is used to break the attack, one drop of Pilocarpine Hydrochloride Ophthalmic Solution 4% should be administered prior to the procedure. Following laser iridoplasty, one drop of Pilocarpine Hydrochloride Ophthalmic Solution 1% should be administered four times daily until an iridotomy can be performed.

    Prevention of Postoperative Elevated IOP Associated with Laser Surgery
    One drop of Pilocarpine Hydrochloride Ophthalmic Solution 1%, 2% or 4% (or two drops administered five minutes apart) should be applied topically in the eye(s) 15 to 60 minutes prior to surgery.

    Induction of Miosis
    One drop of Pilocarpine Hydrochloride Ophthalmic Solution 1%, 2% or 4% (or two drops administered five minutes apart) should be applied topically in the eye(s).

    Use with Other Topical Ophthalmic Medications
    Pilocarpine may be used in combination with beta-blockers, carbonic anhydrase inhibitors, sympathomimetics or hyperosmotic agents. If more than one topical ophthalmic drug is being used, the drugs should be administered at least five (5) minutes apart.

    Use in Pediatric Patients
    In children under 2 years of age, one drop of Pilocarpine Hydrochloride Ophthalmic Solution 1% should be applied topically in the eye(s) three times daily. Children 2 years of age and over should be dosed as for adults. For the induction of miosis prior to goniotomy or trabeculotomy in children, one drop of Pilocarpine Hydrochloride Ophthalmic Solution 1% or 2% should be applied topically in the eye 15 to 60 minutes prior to surgery.

    Dosage Forms and Strengths
    Bottle filled with 15 mL of 1% (10 mg/mL), 2% (20 mg/mL) or 4% (40 mg/mL) pilocarpine hydrochloride sterile ophthalmic solution.


    Contraindications
    None.

    Warnings and Precautions
    Poor Illumination
    Patients should be advised to exercise caution in night driving and other hazardous occupations in poor illumination. In addition, miotics may cause accommodative spasm. Patients should be advised not to drive or use machinery if vision is not clear.

    Pre-existing Retinal Disease
    As with all miotics, rare cases of retinal detachment have been reported when used in certain susceptible individuals and those with pre-existing retinal disease; therefore, a thorough examination of the retina including funduscopy is advised in all patients prior to the initiation of therapy.

    Iritis
    Pilocarpine Hydrochloride Ophthalmic Solution is not recommended to be used when iritis is present.

    Primary Congenital Glaucoma
    Caution is advised when using Pilocarpine Hydrochloride Ophthalmic Solution in pediatric patients with primary congenital glaucoma for control of intraocular pressure (IOP) as cases of a paradoxical increase in IOP have been reported. In addition, the use of Pilocarpine Hydrochloride Ophthalmic Solution is not recommended in pediatric patients diagnosed with glaucoma secondary to anterior segment dysgenesis or uveitis (especially if uveitis is active).

    Contact Lens Wear
    Contact lens wearers should be advised to remove their lenses prior to the instillation of Pilocarpine Hydrochloride Ophthalmic Solution and to wait 10 minutes after dosing before reinserting their contact lenses.

    Adverse Reactions
    Clinical Studies Experience
    Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.
    The safety data described below reflect exposure in four controlled clinical trials of 90 days to 2 years duration in 317 patients diagnosed with open-angle glaucoma or ocular hypertension. In the four clinical trials, patients were treated with Pilocarpine Hydrochloride Ophthalmic Solution 2%, two to four times daily or with Pilocarpine Hydrochloride Ophthalmic Solution 1%, 1.75% or 2% in fixed combination with betaxolol 0.25%, two or three times daily. The most frequently reported adverse reactions occurring in ≥ 5% of patients in the pilocarpine 2% populations were: headache/browache, accommodative change, blurred vision, eye irritation, visual impairment (dim, dark, or "jumping" vision), and eye pain.
    The adverse reaction profile reported for the use of Pilocarpine Hydrochloride Ophthalmic Solution in pediatric patients is comparable to that seen in adult patients.

    USE IN SPECIFIC POPULATION

    Pregnancy
    Pregnancy. Category C. Animal reproduction studies have not been conducted with pilocarpine hydrochloride. It is also not known whether pilocarpine hydrochloride can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Pilocarpine Hydrochloride Ophthalmic Solution should be given to a pregnant woman only if clearly needed.

    Nursing Mothers
    It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when Pilocarpine Hydrochloride Ophthalmic Solution is administered to a nursing woman.

    Pediatric Use
    Safety and effectiveness of pilocarpine hydrochloride ophthalmic solution in pediatric patients have been established.

    Geriatric Use
    No overall differences in safety or effectiveness have been observed between elderly and younger patients.

    Overdosage
    Systemic toxicity following topical ocular administration of pilocarpine is rare, but occasionally patients who are sensitive may develop sweating and gastrointestinal overactivity following the suggested dosage and administration. Overdosage can produce sweating, salivation, nausea, tremors and slowing of the pulse and a decrease in blood pressure. In moderate overdosage, spontaneous recovery is to be expected and is aided by intravenous fluids to compensate for dehydration. For patients demonstrating severe poisoning, atropine, the pharmacologic antagonist to pilocarpine, should be used.







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