Label: PHOSPHOLINE IODIDE OPHTHALMIC- echothiophate iodide   

  • NDC Code(s): 0046-1065-05, 0046-1162-05, 0046-1265-05
  • Packager: Wyeth Pharmaceuticals Inc.
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: New Drug Application

Drug Label Information

Updated 04/10

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  • SPL UNCLASSIFIED SECTION

    Rx Only

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  • DESCRIPTION

    Chemical name: (2-mercaptoethyl) trimethylammonium iodide O,O-diethyl phosphorothioate

    Structural formula

    Structural Formula

    Echothiophate iodide for ophthalmic solution occurs as a white, crystalline, water-soluble, hygroscopic solid having a slight mercaptan-like odor. When freeze-dried in the presence of potassium acetate, the mixture appears as a white amorphous deposit on the walls of the bottle.

    Each package contains materials for dispensing 5 mL of eyedrops: (1) bottle containing sterile echothiophate iodide for ophthalmic solution in one of four potencies [1.5 mg (0.03%), 3 mg (0.06%), 6.25 mg (0.125%), or 12.5 mg (0.25%)] as indicated on the label, with 40 mg potassium acetate in each case. Sodium hydroxide or acetic acid may have been incorporated to adjust pH during manufacturing. (2) a 5 mL bottle of sterile diluent containing chlorobutanol (chloral derivative), 0.55%; mannitol, 1.2%; boric acid, 0.06%; and sodium phosphate, 0.026%. (3) sterilized dropper.

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  • CLINICAL PHARMACOLOGY

    Echothiophate iodide for ophthalmic solution is a long-acting cholinesterase inhibitor for topical use which enhances the effect of endogenously liberated acetylcholine in iris, ciliary muscle, and other parasympathetically innervated structures of the eye. It thereby causes miosis, increase in facility of outflow of aqueous humor, fall in intraocular pressure, and potentiation of accommodation.

    Echothiophate iodide for ophthalmic solution will depress both plasma and erythrocyte cholinesterase levels in most patients after a few weeks of eyedrop therapy.

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  • INDICATIONS AND USAGE

    Glaucoma

    Chronic open-angle glaucoma. Subacute or chronic angle-closure glaucoma after iridectomy or where surgery is refused or contraindicated. Certain non-uveitic secondary types of glaucoma, especially glaucoma following cataract surgery.

    Accommodative Esotropia

    Concomitant esotropias with a significant accommodative component.

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  • CONTRAINDICATIONS

    1. Active uveal inflammation.
    2. Most cases of angle-closure glaucoma, due to the possibility of increasing angle block.
    3. Hypersensitivity to the active or inactive ingredients.
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  • WARNINGS

    1. Succinylcholine should be administered only with great caution, if at all, prior to or during general anesthesia to patients receiving anticholinesterase medication because of possible respiratory or cardiovascular collapse.

    2. Caution should be observed in treating glaucoma with echothiophate iodide for ophthalmic solution in patients who are at the same time undergoing treatment with systemic anticholinesterase medications for myasthenia gravis, because of possible adverse additive effects.

    (See “PRECAUTIONS, Drug Interactions” for further information.)

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  • PRECAUTIONS

    General

    1. Gonioscopy is recommended prior to initiation of therapy. Routine examination to detect lens opacity should accompany clinical use of echothiophate iodide for ophthalmic solution.

    2. Where there is a quiescent uveitis or a history of this condition, anticholinesterase therapy should be avoided or used cautiously because of the intense and persistent miosis and ciliary muscle contraction that may occur.

    3. While systemic effects are infrequent, proper use of the drug requires digital compression of the nasolacrimal ducts for a minute or two following instillation to minimize drainage into the nasal chamber with its extensive absorption area. To prevent possible skin absorption, hands should be washed following instillation.

    4. Temporary or permanent discontinuance of medication is necessary if cardiac irregularities occur.

    5. Anticholinesterase drugs should be used with extreme caution, if at all, in patients with marked vagotonia, bronchial asthma, spastic gastrointestinal disturbances, peptic ulcer, pronounced bradycardia and hypotension, recent myocardial infarction, epilepsy, parkinsonism, and other disorders that may respond adversely to vagotonic effects.

    6. Anticholinesterase drugs should be employed prior to ophthalmic surgery only as a considered risk because of the possible occurrence of hyphema.

    7. Echothiophate iodide for ophthalmic solution should be used with great caution, if at all, where there is a prior history of retinal detachment.

    8. Temporary discontinuance of medication is necessary if salivation, urinary incontinence, diarrhea, profuse sweating, muscle weakness, or respiratory difficulties occur.

    9. Patients receiving echothiophate iodide for ophthalmic solution who are exposed to carbamate- or organophosphate-type insecticides and pesticides (professional gardeners, farmers, workers in plants manufacturing or formulating such products, etc.) should be warned of the additive systemic effects possible from absorption of the pesticide through the respiratory tract or skin. During periods of exposure to such pesticides, the wearing of respiratory masks, and frequent washing and clothing changes may be advisable.

    Drug Interactions

    Echothiophate iodide for ophthalmic solution potentiates other cholinesterase inhibitors such as succinylcholine or organophosphate and carbamate insecticides. Patients undergoing systemic anticholinesterase treatment should be warned of the possible additive effects of echothiophate iodide for ophthalmic solution.

    Carcinogenesis, Mutagenesis, Impairment of Fertility

    No data is available regarding carcinogenesis, mutagenesis, and impairment of fertility.

    Pregnancy

    Teratogenic Effects – Pregnancy Category C

    Animal reproduction studies have not been conducted with echothiophate iodide for ophthalmic solution. It is also not known whether echothiophate iodide for ophthalmic solution can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Echothiophate iodide for ophthalmic solution should be given to a pregnant woman only if clearly needed.

    Nursing Mothers

    Because of the potential for serious adverse reactions in nursing infants from echothiophate iodide for ophthalmic solution, a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother.

    Pediatric Use

    Safety and effectiveness in pediatric patients have been established.

    Geriatric Use

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

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  • ADVERSE REACTIONS

    1. Although the relationship, if any, of retinal detachment to the administration of echothiophate iodide for ophthalmic solution has not been established, retinal detachment has been reported in a few cases during the use of echothiophate iodide for ophthalmic solution in adult patients without a previous history of this disorder.

    2. Stinging, burning, lacrimation, lid muscle twitching, conjunctival and ciliary redness, browache, induced myopia with visual blurring may occur.

    3. Activation of latent iritis or uveitis may occur.

    4. Iris cysts may form, and if treatment is continued, may enlarge and obscure vision. This occurrence is more frequent in children. The cysts usually shrink upon discontinuance of the medication, reduction in strength of the drops or frequency of instillation. Rarely, they may rupture or break free into the aqueous. Regular examinations are advisable when the drug is being prescribed for the treatment of accommodative esotropia.

    5. Prolonged use may cause conjunctival thickening, obstruction of nasolacrimal canals.

    6. Lens opacities occurring in patients under treatment for glaucoma with echothiophate iodide for ophthalmic solution have been reported and similar changes have been produced experimentally in normal monkeys. Routine examinations should accompany clinical use of the drug.

    7. Paradoxical increase in intraocular pressure may follow anticholinesterase instillation. This may be alleviated by prescribing a sympathomimetic mydriatic such as phenylephrine.

    8. Cardiac irregularities.

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  • DOSAGE AND ADMINISTRATION

    DIRECTIONS FOR PREPARING EYEDROPS

    1. Use aseptic technique.

    2. Tear off aluminum seals, and remove and discard rubber plugs from both drug and diluent containers.

    3. Pour diluent into drug container.

    4. Remove dropper assembly from its sterile wrapping. Holding dropper assembly by the screw cap and, WITHOUT COMPRESSING RUBBER BULB, insert into drug container and screw down tightly.

    5. Shake for several seconds to ensure mixing.

    6. Do not cover nor obliterate instructions to patient regarding storage of eyedrops.

    Glaucoma

    Selection of Therapy – The medication prescribed should be that which will control the intraocular pressure around-the-clock with the least risk of side effects or adverse reactions. “Tonometric glaucoma” (ocular hypertension without other evidence of the disease) is frequently not treated with any medication, and echothiophate iodide for ophthalmic solution is certainly not recommended for this condition. In early chronic simple glaucoma with field loss or disc changes, pilocarpine is generally used for initial therapy and can be recommended so long as control is thereby maintained over the 24 hours of the day.

    When this is not the case, echothiophate iodide for ophthalmic solution 0.03% may be effective and probably has no greater potential for side effects. If this dosage is inadequate, epinephrine and a carbonic anhydrase inhibitor may be added to the regimen. When still more effective medication is required, the higher strengths of echothiophate iodide for ophthalmic solution may be prescribed with the recognition that the control of the intraocular pressure should have priority regardless of potential side effects. In secondary glaucoma following cataract surgery, the higher strengths of the drug are frequently needed and are ordinarily very well tolerated.

    The dosage regimen prescribed should call for the lowest concentration that will control the intraocular pressure around-the-clock. Where tonometry around-the-clock is not feasible, it is suggested that appointments for tension-taking be made at different times of the day so that inadequate control may be more readily detected. Two doses a day are preferred to one in order to maintain as smooth a diurnal tension curve as possible, although a single dose per day or every other day has been used with satisfactory results. Because of the long duration of action of the drug, it is never necessary or desirable to exceed a schedule of twice a day. The daily dose or one of the two daily doses should always be instilled just before retiring to avoid inconvenience due to the miosis.

    Early Chronic Simple Glaucoma – Echothiophate iodide for ophthalmic solution 0.03% instilled twice a day, just before retiring and in the morning, may be prescribed advantageously for cases of early chronic simple glaucoma that are not controlled around-the-clock with other less potent agents. Because of prolonged action, control during the night and early morning hours may then sometimes be obtained. A change in therapy is indicated if, at any time, the tension fails to remain at an acceptable level on this regimen.

    Advanced Chronic Simple Glaucoma and Glaucoma Secondary to Cataract Surgery – These cases may respond satisfactorily to echothiophate iodide for ophthalmic solution 0.03% twice a day as above. When the patient is being transferred to echothiophate iodide for ophthalmic solution because of unsatisfactory control with pilocarpine, carbachol, epinephrine, etc., one of the higher strengths, 0.06%, 0.125%, or 0.25% will usually be needed. In this case, a brief trial with the 0.03% eyedrops will be advantageous in that the higher strengths will then be more easily tolerated.

    Concomitant Therapy – Echothiophate iodide for ophthalmic solution may be used concomitantly with epinephrine, a carbonic anhydrase inhibitor, or both.

    Technique – Good technique in the administration of echothiophate iodide for ophthalmic solution requires that finger pressure at the inner canthus should be exerted for a minute or two following instillation of the eyedrops, to minimize drainage into the nose and throat. Excess solution around the eye should be removed with tissue and any medication on the hands should be rinsed off.

    Accommodative Esotropia (Pediatric Use)

    In Diagnosis – One drop of 0.125% may be instilled once a day in both eyes on retiring, for a period of two or three weeks. If the esotropia is accommodative, a favorable response will usually be noted which may begin within a few hours.

    In Treatment – Echothiophate iodide for ophthalmic solution is prescribed at the lowest concentration and frequency which gives satisfactory results. After the initial period of treatment for diagnostic purposes, the schedule may be reduced to 0.125% every other day or 0.06% every day. These dosages can often be gradually lowered as treatment progresses. The 0.03% strength has proven to be effective in some cases. The maximum usually recommended dosage is 0.125% once a day, although more intensive therapy has been used for short periods.

    Technique – (See “DOSAGE AND ADMINISTRATION, Glaucoma.”)

    Duration of Treatment – In diagnosis, only a short period is required and little time will be lost in instituting other procedures if the esotropia proves to be unresponsive. In therapy, there is no definite limit so long as the drug is well tolerated. However, if the eyedrops, with or without eyeglasses, are gradually withdrawn after about a year or two and deviation recurs, surgery should be considered. As with other miotics, tolerance may occasionally develop after prolonged use. In such cases, a rest period will restore the original activity of the drug.

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  • HOW SUPPLIED

    Each package contains sterile echothiophate iodide for ophthalmic solution, sterile diluent, and dropper for dispensing 5 mL eyedrops of the strength indicated on the label. Four potencies are available:

    NDC 0046-1062-05 . . . . . . . . . . . . . . . . . 1.5 mg package for 0.03%

    White amorphous deposit on bottle walls. Aluminum crimp seal is blue.

    NDC 0046-1064-05 . . . . . . . . . . . . . . . . . 3 mg package for 0.06%

    White amorphous deposit on bottle walls. Aluminum crimp seal is red.

    NDC 0046-1065-05 . . . . . . . . . . . . . . . . . 6.25 mg package for 0.125%

    White amorphous deposit on bottle walls. Aluminum crimp seal is green.

    NDC 0046-1066-05 . . . . . . . . . . . . . . . . . 12.5 mg package for 0.25%

    White amorphous deposit on bottle walls. Aluminum crimp seal is yellow.

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  • HANDLING AND STORAGE:

    Prior to reconstitution: Store under refrigeration (2° to 8° C).

    After reconstitution: Store at room temperature (approximately 25° C). Do not refrigerate. Discard any unused solution after 4 weeks.



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    Wyeth®

    Manufactured for

    Wyeth Pharmaceuticals Inc.

    Philadelphia, PA 19101

    by CANGENE bioPharma

    Baltimore, MD 21230

    W10441C006

    ET01

    Rev 04/10

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  • PRINCIPAL DISPLAY PANEL

    PACKAGE LABEL - PRINCIPAL DISPLAY - 5 ML - DILUENT LABEL

    NDC 0046-1162-05

    STERILE DILUENT FOR PREPARING

    Phospholine Iodide®

    (echothiophate iodide for ophthalmic solution)

    EYEDROPS

    5 mL (1/6 fl oz)

    Wyeth®

    Principal Display Panel - 5 mL - Diluent Label
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  • PRINCIPAL DISPLAY PANEL

    PACKAGE LABEL - PRINCIPAL DISPLAY - 6.25 MG/5 ML - LABEL

    NDC 0046-1265-05

    Phospholine Iodide®

    (echothiophate iodide for ophthalmic solution)

    0.125%

    (1/8%)

    6.25 mg/5 mL

    Each 5 mL contains 6.25 mg of echothiophate iodide

    With 40 mg Potassium Acetate for preparing 5 mL eyedrops.

    See accompanying descriptive literature.

    Rx only

    Wyeth®

    Principal Display Panel - 6.25 mg/ 5 mL - Label
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  • PRINCIPAL DISPLAY PANEL

    PACKAGE LABEL - PRINCIPAL DISPLAY - 6.25 MG/5 ML - CARTON

    NDC 0046-1065-05

    Phospholine Iodide®

    (echothiophate iodide for ophthalmic solution)

    0.125%

    (1/8%)

    6.25 mg/5 mL

    This package contains sterile echothiophate iodide with 40 mg potassium acetate (sodium hydroxide or acetic acid may have been incorporated to adjust pH during manufacturing) and 5 mL (1/6 fl oz) sterile aqueous diluent, in individual bottles for dispensing 5 mL of eyedrops of strength shown when reconstituted.

    Rx only

    Wyeth®

    Principal Display Panel - 6.25 mg/ 5 mL - Carton
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  • INGREDIENTS AND APPEARANCE
    PHOSPHOLINE IODIDE  OPHTHALMIC
    echothiophate iodide kit
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:0046-1065
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0046-1065-05 1 in 1 KIT
    Quantity of Parts
    Part # Package Quantity Total Product Quantity
    Part 1 1 BOTTLE 6.25 mL
    Part 2 1 BOTTLE 5 mL
    Part 1 of 2
    PHOSPHOLINE IODIDE  OPHTHALMIC
    echothiophate iodide powder, for solution
    Product Information
    Item Code (Source) NDC:0046-1265
    Route of Administration OPHTHALMIC DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ECHOTHIOPHATE IODIDE (ECHOTHIOPHATE) ECHOTHIOPHATE 6.25 mg  in 5 mL
    Inactive Ingredients
    Ingredient Name Strength
    POTASSIUM ACETATE 40 mg  in 5 mL
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0046-1265-05 6.25 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    NDA NDA011963 12/04/1959
    Part 2 of 2
    PHOSPHOLINE IODIDE  STERILE DILUENT
    echothiophate iodide solution
    Product Information
    Item Code (Source) NDC:0046-1162
    Route of Administration OPHTHALMIC DEA Schedule     
    Inactive Ingredients
    Ingredient Name Strength
    CHLOROBUTANOL 27.5 mg  in 5 mL
    MANNITOL 60 mg  in 5 mL
    BORIC ACID 3 mg  in 5 mL
    SODIUM PHOSPHATE 1.3 mg  in 5 mL
    WATER 5 mL  in 5 mL
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0046-1162-05 5 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    NDA NDA011963 12/04/1959
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    NDA NDA011963 12/04/1959
    Labeler - Wyeth Pharmaceuticals Inc. (828831441)
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