Dosing & Uses
Dosage Forms & Strengths
ophthalmic gel
- 3% (24mg chloroprocaine/800mg gel) as 1.25mL single-use vial
Ocular Surface Anesthesia
Topical gel indicated for ocular surface anesthesia
Apply 3 gtts topically to ocular surface in area of planned procedure
May reapply as needed to maintain anesthetic effect
Safety and efficacy not established
Adverse Effects
>10%
Mydriasis (26%)
Conjunctival hyperemia (11%)
1-10%
Eye irritation (6%)
Warnings
Contraindications
History of hypersensitivity to product components
Cautions
Not for injection or intraocular administration
Corneal injury due to insensitivity may occur; instruct patients to not touch their eye(s) for at least 10-20 minutes after anesthetic applied to avoid accidental injuries
Prolonged use of topical ocular anesthetic may produce permanent corneal opacification and ulceration with accompanying visual loss
Do not touch dropper tip to any surface to avoid contaminating the gel
Indicated for administration under the direct supervision of a healthcare provider; not intended for patient self-administration
Warnings
Pregnancy
There are no adequate and well-controlled studies regarding use in pregnant females to inform of a drug associated risk
There are no animal reproduction studies
Lactation
There are no data on presence of drug in human milk, effects on breastfed infants, or effects on milk production
Pharmacology
Mechanism of Action
As with other local anesthetics, blocks generation and conduction of nerve impulses, presumably by increasing the threshold for electrical excitation in the nerve, by slowing the propagation of the nerve impulse, and by reducing the rate of rise of the action potential
Progression of anesthesia is related to diameter, myelination, and conduction velocity of affected nerve fibers
Clinically, the order of loss of nerve function is as follows: (1) pain, (2) temperature, (3) touch, (4) proprioception, and (5) skeletal muscle tone
Absorption
Systemic exposure to chloroprocaine following topical ocular administration has not been studied
Metabolism
Metabolized by plasma pseudocholinesterases and nonspecific esterases in ocular tissues
Rapidly metabolized in plasma by hydrolysis of ester linkage by pseudocholinesterase; hydrolysis results in beta-diethylaminoethanol and 2-chloro-4-aminobenzoic acid, which inhibit sulfonamides action
Elimination
Half-life: ~25 seconds (adults); ~43 seconds (neonates)
Excretion: Mainly excreted by kidney; urinary excretion affected by urinary perfusion and factors affecting urinary pH
Administration
Ophthalmic Administration
For topical ophthalmic use
Do not inject or intraocularly administer
Discard after use
Storage
Store at 15-25ºC (59-77ºF)
Images
Formulary
Adding plans allows you to compare formulary status to other drugs in the same class.
To view formulary information first create a list of plans. Your list will be saved and can be edited at any time.
Adding plans allows you to:
- View the formulary and any restrictions for each plan.
- Manage and view all your plans together – even plans in different states.
- Compare formulary status to other drugs in the same class.
- Access your plan list on any device – mobile or desktop.