Quốc gia: Hoa Kỳ
Ngôn ngữ: Tiếng Anh
Nguồn: NLM (National Library of Medicine)
Latanoprost (UNII: 6Z5B6HVF6O) (Latanoprost - UNII:6Z5B6HVF6O)
MWI
Latanoprost
Latanoprost 50 ug in 1 mL
OPHTHALMIC
PRESCRIPTION DRUG
Latanoprost ophthalmic solution is indicated for the reduction of elevated intraocular pressure in patients with open-angle glaucoma or ocular hypertension. Known hypersensitivity to latanoprost, benzalkonium chloride, or any other ingredients in this product. Teratogenic Effects: Pregnancy Category C. Reproduction studies have been performed in rats and rabbits. In rabbits, an incidence of 4 of 16 dams had no viable fetuses at a dose that was approximately 80 times the maximum human dose, and the highest nonembryocidal dose in rabbits was approximately 15 times the maximum human dose. There are no adequate and well-controlled studies in pregnant women. Latanoprost ophthalmic solution should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. It is not known whether this drug or its metabolites are excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when latanoprost ophthalmic solution is administered to a nursing wom
Latanoprost Ophthalmic Solution, 0.005% is a clear, isotonic, buffered, preserved colorless solution of latanoprost 0.005% (50 mcg/mL). It is supplied as a 2.5 mL solution in a 5 mL clear low density polyethylene bottle with a clear low density polyethylene dropper tip, and a turquoise polyethylene screw cap. NDC 13985-610-02 2.5 mL fill, 0.005% (50 mcg/mL) Storage: Protect from light. Store unopened bottle(s) under refrigeration at 2° to 8°C (36° to 46°F). During shipment to the patient, the bottle may be maintained at temperatures up to 40°C (104°F) for a period not exceeding 8 days. Once a bottle is opened for use, it may be stored at room temperature up to 25°C (77°F) for 6 weeks.
Abbreviated New Drug Application
LATANOPROST- LATANOPROST SOLUTION/ DROPS MWI ---------- HIGHLIGHTS OF PRESCRIBING INFORMATION THESE HIGHLIGHTS DO NOT INCLUDE ALL THE INFORMATION NEEDED TO USE LATANOPROST OPHTHALMIC SOLUTION SAFELY AND EFFECTIVELY. SEE FULL PRESCRIBING INFORMATION FOR LATANOPROST OPHTHALMIC SOLUTION. LATANOPROST OPHTHALMIC SOLUTION, 0.005% INITIAL U.S. APPROVAL: 1996 INDICATIONS AND USAGE Latanoprost ophthalmic solution is a prostaglandin F analog indicated for the reduction of elevated intraocular pressure in patients with open-angle glaucoma or ocular hypertension. (1) DOSAGE AND ADMINISTRATION One drop in the affected eye(s) once daily in the evening. (2) DOSAGE FORMS AND STRENGTHS Ophthalmic solution containing 50 mcg/mL latanoprost (0.005%). (3) CONTRAINDICATIONS Known hypersensitivity to latanoprost, benzalkonium chloride or any other ingredients in this product. (4) WARNINGS AND PRECAUTIONS Pigmentation: Pigmentation of the iris, periorbital tissue (eyelid) and eyelashes can occur. Iris pigmentation likely to be permanent. (5.1) Eyelash Changes: Gradual change to eyelashes including increased length, thickness and number of lashes. Usually reversible. (5.2) ADVERSE REACTIONS Most common adverse reactions (≥4%) from clinical trials are blurred vision, burning and stinging, conjunctival hyperemia, foreign body sensation, itching, increased pigmentation of the iris, punctate keratitis, and upper respiratory tract infection/nasopharyngitis/influenza. (6) TO REPORT SUSPECTED ADVERSE REACTIONS, CONTACT AKORN, INC. AT 1-800-932-5676 OR FDA AT 1-800-FDA-1088 OR _WWW.FDA.GOV/MEDWATCH_. DRUG INTERACTIONS _In vitro_ studies have shown that precipitation occurs when eye drops containing thimerosal are mixed with latanoprost ophthalmic solution. If such drugs are used, they should be administered at least 5 minutes apart. (7) SEE 17 FOR PATIENT COUNSELING INFORMATION. REVISED: 7/2017 FULL PRESCRIBING INFORMATION: CONTENTS* 1 INDICATIONS AND USAGE 2 DOSAGE AND ADMINISTRATION 3 DOSAGE FORMS AND STRENGTHS 4 CONTRAINDICATIONS 5 WARNINGS Đọc toàn bộ tài liệu