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Econochlor

Alcon Laboratories, Inc.

Econochlor®chloramphenicolSterile OphthalmicSolution and Ointment


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Bone marrow hypoplasia, including aplastic anemia and death has been reported following local application of chloramphenicol. Chloramphenicol should not be used when less potentially dangerous agents would be expected to provide effective treatment.

DESCRIPTION

ECONOCHLOR® (Chloramphenicol) is a sterile topical ophthalmic antibacterial prepared in solution and ointment forms. The active ingredient is represented by the chemical structure:

Econochlor

Established name:

Chloramphenicol

Chemical name:

Acetamide, 2,2-dichloro-N-[2-hydroxy-1-(hydroxymethyl)-2- (4-nitrophenyl) ethyl]-, [R-(R*,R)]-

Each ml of solution contains: Active: Chloramphenicol 0.5% (5mg/ml). Preservative: Thimerosal 0.01%. Vehicle: Hydroxypropyl Methylcellulose: Inactive: Boric Acid, Sodium Borate (to adjust pH), Purified Water.

DM-00

Each gram of ointment contains: Active: Chloramphenicol 1.0% (10 mg/g). Inactive: Mineral Oil, Anhydrous Liquid Lanolin, White Petrolatum.

DM-00

CLINICAL PHARMACOLOGY

Chloramphenicol is a broad-spectrum antibiotic originally isolated from Streptomyces venezuelae. It is primarily bacteriostatic and acts by inhibition of protein synthesis by interfering with the transfer of activated amino acids from soluble RNA to ribosomes. Development of resistance to chloramphenicol can be regarded as minimal for staphylococci and many other species of bacteria.

INDICATIONS USAGE

Chloramphenicol should be used only in those serious infections for which less potentially dangerous drugs are ineffective or contraindicated. Bacteriological studies should be performed to determine the causative organisms and their sensitivity to chloramphenicol (See Box Warning). For treatment of ocular infections involving the conjunctiva and/or cornea caused by chloramphenicol-susceptible organisms.

Chloramphenicol has a wide spectrum of antimicrobial activity and is effective against many gram negative and gram positive bacteria, including the following common eye pathogens:

Staphylococcus aureus

Streptococci, including Streptococcus pneumoniae

Escherichia coli

Haemophilus influenzae

Klebsiella/Enterobacter species

Neisseria species

Moraxella lacunata (Morax-Axenfeld bacillus)

The product does not provide adequate coverage against:

Pseudomonas aeruginosa

Serratia marcescens

CONTRAINDICATIONS

This product is contraindicated in those persons who have shown hypersensitivity to any of its components.

WARNINGS

SEE BOX WARNING.

Ophthalmic ointment may retard corneal wound healing.

PRECAUTIONS

Prolonged use of antibiotics may occasionally result in overgrowth of non-susceptible organisms, including fungi. If new infections appear during treatment, the therapy should be altered. In all serious infections, the topical use of chloramphenicol should be supplemented by appropriate systemic medication.

ADVERSE REACTIONS

Blood dyscrasias may be associated with the systemic use of chloramphenicol. One case of bone-marrow hypoplasia following the prolonged (23 month) topical use of chloramphenicol ophthalmic solution has been reported.

DOSAGE ADMINISTRATION

Solution: In severe disease, instill two drops on the eye(s) hourly until improvement, following which treatment should be diminished prior to discontinuation. In mild disease, drops may be used four times daily. Ointment: Apply a small amount to the lower conjunctival sac(s) at bedtime as a supplement to the drops.

HOW SUPPLIED

Solution in 5ml (2.5ml fill) and 15ml plastic Drop-Tainer® dispensers. Ointment in 3.5 gram ophthalmic tube. Rx only.

2.5ml NDC 0065-0642-25

15ml NDC 0065-0642-15

3.5 g NDC 0065-0641-35

STORAGE

Solution: Refrigerate until dispensed. Ointment: Store between 46° and 80°F.

June, 1984
29824
Printed in USA

Alcon
Alcon Laboratories, Inc.
Fort Worth, Texas 76134 USA

Econochlor

chloramphenicol SOLUTION

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:0065-0642
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
chloramphenicol CHLORAMPHENICOL 5 mg

Inactive Ingredients

Ingredient Name Strength
THIMEROSAL
hydroxypropyl methylcellulose
BORIC ACID
SODIUM BORATE
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0065-0642-25 2.5 in 1 BOTTLE, PLASTIC
2 NDC:0065-0642-15 15 in 1 BOTTLE, PLASTIC



Econochlor

chloramphenicol OINTMENT

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:0065-0641
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
chloramphenicol CHLORAMPHENICOL 10 mg

Inactive Ingredients

Ingredient Name Strength
Mineral Oil
anhydrous liquid lanolin
white petrolatum

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0065-0641-35 3.5 in 1 TUBE



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