PREDNISOLONE ACETATE suspension/ drops

Krajina: Spojené štáty

Jazyk: angličtina

Zdroj: NLM (National Library of Medicine)

Aktívna zložka:

PREDNISOLONE ACETATE (UNII: 8B2807733D) (PREDNISOLONE - UNII:9PHQ9Y1OLM)

Dostupné z:

Pacific Pharma, Inc.

Spôsob podávania:

OPHTHALMIC

Typ predpisu:

PRESCRIPTION DRUG

Terapeutické indikácie:

Prednisolone acetate ophthalmic suspension 1% is indicated for the treatment of steroid-responsive inflammation of the palpebral and bulbar conjunctiva, cornea, and anterior segment of the globe. Prednisolone acetate ophthalmic suspension 1% is contraindicated in acute untreated purulent ocular infections, in most viral diseases of the cornea and conjunctiva including epithelial herpes simplex keratitis (dendritic keratitis), vaccinia, and varicella, and also in mycobacterial infection of the eye and fungal diseases of ocular structures. Prednisolone acetate ophthalmic suspension 1% is also contraindicated in individuals with known or suspected hypersensitivity to any of the ingredients of this preparation and to other corticosteroids.

Prehľad produktov:

Prednisolone acetate ophthalmic suspension, USP 1% is supplied sterile in opaque white LDPE plastic bottles with droppers with pink high impact polystyrene (HIPS) caps as follows: 5 mL in 10 mL bottle - NDC 60758-119-05 10 mL in 15 mL bottle - NDC 60758-119-10 15 mL in 15 mL bottle - NDC  60758-119-15 Store at up to 25°C (77°F). Protect from freezing. Store in an upright position. Revised: 05/2020 Distributed by: Allergan USA, Inc. Madison, NJ 07940 © 2020 Allergan. All rights reserved. All trademarks are the property of their respective owners. v1.2USPI0119

Stav Autorizácia:

New Drug Application Authorized Generic

Súhrn charakteristických

PREDNISOLONE ACETATE- PREDNISOLONE ACETATE SUSPENSION/ DROPS
PACIFIC PHARMA, INC.
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PREDNISOLONE ACETATE
OPHTHALMIC SUSPENSION, USP 1%
STERILE
DESCRIPTION
Prednisolone acetate ophthalmic suspension, USP 1% is a sterile,
topical anti-inflammatory agent for
ophthalmic use. Its chemical name is 11ß,17,
21-Trihydroxypregna-1,4-diene-3, 20-dione 21-acetate
and it has the following structure:
STRUCTURAL FORMULA:
prednisolone acetate
Each mL of prednisolone acetate ophthalmic suspension 1% contains:
ACTIVE: prednisolone acetate (microfine suspension) 1%
INACTIVES: benzalkonium chloride as preservative; boric acid; edetate
disodium; hypromellose;
polysorbate 80; purified water; sodium bisulfite; sodium chloride; and
sodium citrate.
The pH during its shelf life ranges from 5.0 - 6.0.
CLINICAL PHARMACOLOGY
Prednisolone acetate is a glucocorticoid that, on the basis of weight,
has 3 to 5 times the anti-
inflammatory potency of hydrocortisone. Glucocorticoids inhibit the
edema, fibrin deposition, capillary
dilation, and phagocytic migration of the acute inflammatory response,
as well as capillary proliferation,
deposition of collagen, and scar formation.
INDICATIONS AND USAGE
Prednisolone acetate ophthalmic suspension 1% is indicated for the
treatment of steroid-
responsive inflammation of the palpebral and bulbar conjunctiva,
cornea, and anterior segment of the
globe.
CONTRAINDICATIONS
Prednisolone acetate ophthalmic suspension 1% is contraindicated in
acute untreated purulent ocular
infections, in most viral diseases of the cornea and conjunctiva
including epithelial herpes simplex
keratitis (dendritic keratitis), vaccinia, and varicella, and also in
mycobacterial infection of the eye and
fungal diseases of ocular structures.
Prednisolone acetate ophthalmic suspension 1% is also contraindicated
in individuals with known or
suspected hypersensitivity to any of the ingredients of this
preparation and to other corticosteroids.
WARNINGS
Prolonged use of corticosteroids may result in posterior subcapsular
cataract for