Epinastine Hydrochloride

DESCRIPTION

Epinastine HClOphthalmicSolution 0.05% is a clear, colorless, sterileisotonic solutioncontaining epinastine HCl, an antihistamine and an inhibitor ofhistaminerelease from themast cellfor topical administration to the eyes.

Epinastine HCl is represented by the following structural formula:

C₁₆H₁₅N₃HCl Mol. Wt. 285.78

Chemical Name

3-Amino-9,13b-dihydro-1H-dibenz[c,f]imidazo [1,5-a]azepine hydrochloride

Each mL Contains

Active:epinastine HCl 0.05% (0.5 mg/mL) equivalent to epinastine 0.044% (0.44 mg/mL);Preservative:benzalkonium chloride 0.01%;Inactives:edetate disodium; water for injection; sodium chloride; sodium phosphate, monobasic; and sodium hydroxide and/or hydrochloric acid (to adjust pH). Epinastine HCl has a pH of approximately 7 and an osmolality range of 250 to 310 mOsm/kg.

INDICATIONS

Epinastine HCl Ophthalmic Solution 0.05% is indicated for the prevention of itching associated with allergic conjunctivitis.

DOSAGE AND ADMINISTRATION

The recommended dosage is one drop in each eye twice a day.

Treatment should be continued throughout the period of exposure (i.e., until the pollen season is over or until exposure to the offending allergen is terminated), even when symptoms are absent.

HOW SUPPLIED

Dosage Forms And Strengths

Solution containing 0.5 mg/mL epinastine HCl

Storage And Handling

Epinastine HCl Ophthalmic Solution 0.05%is supplied sterile in opaque white LDPE plastic bottles with dropper tips and white polypropylene (PP) caps as follows:

5 mL in 10 mL bottleNDC51991-836-75

Storage

存储在20°- 25°C (68° - 77°F) [seeUSP Controlled Room Temperature]. Keep bottle tightly closed and out of the reach of children.

Distributed by: Breckenridge Pharmaceutical, Inc., Berlin, CT 06037. Manufactured by: Defender SD Manufacturing, LLC., San Diego, CA 92121. Revised: Nov 2021

SIDE EFFECTS

Clinical Studies Experience

Because clinical studies are conducted under widely varying conditions, adverse reaction rates observed in the clinical studies of a drug cannot be directly compared to rates in the clinical studies of another drug and may not reflect the rates observed in practice.

The most frequently reported ocular adverse reactions occurring in approximately 1-10% of patients were burning sensation in the eye, folliculosis, hyperemia, and pruritus.

The most frequently reported non-ocular adverse reactions were infection (cold symptoms and upper respiratory infections), seen in approximately 10% of patients, and headache, rhinitis, sinusitis, increased cough, and pharyngitis, seen in approximately 1 - 3% of patients.

Some of these reactions were similar to the underlying disease being studied.

Postmarketing Experience

The following reactions have been identified during postmarketing use of Epinastine HCl Ophthalmic Solution 0.05% in clinical practice. Because they are reported voluntarily from a population of unknown size, estimates of frequency cannot be made. The reactions, which have been chosen for inclusion due to either their seriousness, frequency of reporting, possible causal connection to Epinastine HCl Ophthalmic Solution 0.05%, or a combination of these factors, include: lacrimation increased.

DRUG INTERACTIONS

No Information provided

警告

Included as part of thePRECAUTIONSsection.

PRECAUTIONS

Contamination Of Tip And Solution

Patients should be instructed to avoid allowing the tip of the dispensing container to contact the eye, surrounding structures, fingers, or any other surface in order to avoid contamination of the solution by common bacteria known to cause ocular infections. Serious damage to the eye and subsequent loss of vision may result from using contaminated solutions.

Bottle should be kept tightly closed when not in use.

Use With Contact Lenses

Patients should be advised not to wear a contact lens if their eye is red. Epinastine HCl Ophthalmic Solution 0.05% should not be used to treat contact lens-related irritation.

The preservative in Epinastine HCl ophthalmic solution 0.05%, benzalkonium chloride, may be absorbed by soft contact lenses. Contact lenses should be removed prior to instillation of Epinastine HCl Ophthalmic Solution 0.05% and may be reinserted after 10 minutes following its administration.

Topical Ophthalmic Use Only

Epinastine HCl Ophthalmic Solution 0.05% is for topical ophthalmic use only and not for injection or oral use.

Nonclinical Toxicology

Carcinogenesis, Mutagenesis, Impairment Of Fertility

In 18-month or 2-year dietary carcinogenicity studies in mice or rats, respectively, epinastine was not carcinogenic at doses up to 40 mg/kg [approximately 30,000 times higher than the MROHD, assuming 100% absorption in humans and animals].

Epinastine in newly synthesized batches was negative for mutagenicity in the Ames/Salmonellaassay and in vitro chromosome aberration assay using human lymphocytes. Positive results were seen with early batches of epinastine in two in vitro chromosomal aberration studies conducted in 1980s with human peripheral lymphocytes and with V79 cells, respectively. Epinastine was negative in the in vivo clastogenicity studies, including the mouse micronucleus assay and chromosome aberration assay in Chinese hamsters. Epinastine was also negative in the cell transformation assay using Syrian hamster embryo cells, V79/HGPRT mammalian cellpoint mutationassay, and in vivo/in vitro unscheduled DNA synthesis assay using rat primary hepatocytes.

Epinastine had no effect on fertility of male rats. Decreased fertility in female rats was observed at an oral dose up to approximately 90,000 times the MROHD.

Use In Specific Populations

Pregnancy

Teratogenic Effects

Pregnancy Category C

In an embryofetal developmental study in pregnant rats, maternal toxicity with no embryofetal effects was observed at an oral dose that was approximately 150,000 times the maximum recommendedocularhuman dose (MROHD) of 0.0014 mg/kg/day on a mg/kg basis. Total resorptions andabortionwere observed in an embryofetal study in pregnant rabbits at an oral dose that was approximately 55,000 times the MROHD. In both studies, no drug-inducedteratogeniceffects were noted.

Epinastine reduced pup body weight gain following an oral dose to pregnant rats that was approximately 90,000 times the MROHD.

There are, however, no adequate and well-controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human response, Epinastine HCl Ophthalmic Solution 0.05% should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.

Nursing Mothers

A study in lactating rats revealed excretion of epinastine in the breast milk. 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 Epinastine HCl Ophthalmic Solution 0.05% is administered to a nursing woman.

Pediatric Use

Safety and effectiveness in pediatric patients below the age of 2 years have not been established.

Geriatric Use

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

OVERDOSE

No Information Provided

CONTRAINDICATIONS

None.

CLINICAL PHARMACOLOGY

Mechanism Of Action

Epinastine is a topically active, direct H -receptorantagonistand an inhibitor of the release of histamine from the mast cell. Epinastine is selective for the histamine H -receptor and hasaffinityfor the histamine H -receptor. Epinastine also possesses affinity for the α1, α2-, and 5-HT2 –receptors.

Pharmacokinetics

Fourteen subjects, with过敏性结膜炎, received one drop of Epinastine HCl Ophthalmic Solution 0.05% in each eye twice daily for 7 days. On day 7, average maximum epinastine plasma concentrations of 0.04±0.014 ng/ml were reached after about two hours indicating low systemic exposure. While these concentrations represented an increase over those seen following a single dose, the day 1 and day 7 Area Under the Curve (AUC) values were unchanged indicating that there is no increase in systemic absorption with multiple dosing. Epinastine is 64% bound to plasma proteins. The total systemic clearance is approximately 56 L/hr and the terminal plasma elimination half-life is about 12 hours. Epinastine is mainly excreted unchanged. About 55% of an intravenous dose is recovered unchanged in the urine with about 30% in feces. Less than 10% is metabolized. The renal elimination is mainly via active tubular secretion.

Clinical Studies

Epinastine HCl 0.05% has been shown to be significantly superior to vehicle for improving ocular itching in patients with allergicconjunctivitisin clinical studies using two different models: (1)conjunctivalantigenchallenge (CAC) where patients were dosed and then received antigen instilled into theinferiorconjunctival fornix; and (2) environmental field studies where patients were dosed and evaluated duringallergyseason in their natural habitat. Results demonstrated a rapid onset of action for epinastine HCl 0.05% within 3 to 5 minutes after conjunctival antigen challenge. Duration of effect was shown to be 8 hours, making a twice daily regimen suitable. This dosing regimen was shown to be safe and effective for up to 8 weeks, without evidence of tachyphylaxis.

PATIENT INFORMATION

Sterility Of Dropper Tip

应该建议患者不要碰滴管p to any surface, as this may contaminate the contents (see警告AND PRECAUTIONS).

Concomitant Use Of Contact Lenses

Patients should be advised not to wear a contactlensif their eye is red. Patients should be advised that Epinastine HCl Ophthalmic Solution 0.05% should not be used to treat contact lens-related irritation. Patients should also be advised to remove contact lenses prior to instillation of Epinastine HCl Ophthalmic Solution 0.05%. The preservative in Epinastine HCl Ophthalmic Solution 0.05%, benzalkonium chloride, may be absorbed by soft contact lenses. Lenses may be reinserted after 10 minutes following administration of Epinastine HCl Ophthalmic Solution 0.05%

Topical Ophthalmic Use Only

For topical ophthalmic administration only.