Miochol E
Generic: ACETYLCHOLINE CHLORIDE
Basic Information
Manufacturer
Bausch & Lomb Incorporated
Product Type
HUMAN PRESCRIPTION DRUG
Route of Administration
FDA Set ID
e701ef07-9499-4b56-931f-f4eb3eedbe24
Indications & Usage
INDICATIONS AND USAGE To obtain miosis of the iris in seconds after delivery of the lens in cataract surgery, in penetrating keratoplasty, iridectomy, and other anterior segment surgery where rapid miosis may be required.
Warnings
WARNINGS DO NOT GAS STERILIZE.
If blister or peelable backing is damaged or broken, sterility of the enclosed vial and ampule cannot be assured.
Open under aseptic conditions only.
If blister or peelable backing is damaged or broken, sterility of the enclosed vial and ampule cannot be assured.
Open under aseptic conditions only.
Adverse Reactions
ADVERSE REACTIONS Infrequent cases of corneal edema, corneal clouding, and corneal decompensation have been reported with the use of intraocular acetylcholine.
Adverse reactions have been reported rarely, which are indicative of systemic absorption.
These include bradycardia, hypotension, flushing, breathing difficulties, and sweating.
To report SUSPECTED ADVERSE REACTIONS, contact Bausch & Lomb Incorporated at 1-800-553-5340 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
Adverse reactions have been reported rarely, which are indicative of systemic absorption.
These include bradycardia, hypotension, flushing, breathing difficulties, and sweating.
To report SUSPECTED ADVERSE REACTIONS, contact Bausch & Lomb Incorporated at 1-800-553-5340 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.