Moxifloxacin (oral): Difference between revisions

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{{Moxifloxacin}}
{{Moxifloxacin}}
{{CMG}};{{AE}}{{AK}}
{{CMG}};{{AE}}{{AK}}
'''''For patient information, click <u>[[Moxiloxacin(patient information)|here]]'''''</u>
'''''For patient information, click <u>[[Moxiloxacin(patient information)|here]]'''''</u>



Revision as of 08:42, 9 January 2014

Moxifloxacin
AVELOX® FDA Package Insert
Description
Clinical Pharmacology
Microbiology
Indications and Usage
Contraindications
Warnings and Precautions
Adverse Reactions
Overdosage
Clinical Studies
Dosage and Administration
How Supplied
Labels and Packages

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1];Associate Editor(s)-in-Chief: Abdurahman Khalil, M.D. [2]

For patient information, click here


Overview

Moxifloxacin is a synthetic fluoroquinolone antibiotic agent. Bayer AG developed the drug (initially called BAY 12-8039) and it is marketed worldwide (as the hydrochloride) under the brand name Avelox® (in some countries also Avalox®) for oral treatment. Each tablet contains 400 mg. In most countries the drug is also available in parenteral form for intravenous infusion. Moxifloxacin is also sold in an ophthalmic solution (eye drops) under the name Vigamox® for the treatment of conjunctivitis.

Category

Fluoroquinolone, fourth generation.

US Brand Names

AVELOX®, MOXEZA®, VIGAMOX®.

FDA Package Insert

Description | Clinical Pharmacology | Microbiology | Indications and Usage | Contraindications | Warnings and Precautions | Adverse Reactions | Overdosage | Clinical Studies | Dosage and Administration | How Supplied | Labels and Packages

References

http://www.accessdata.fda.gov/drugsatfda_docs/label/2004/21277slr018,21085slr023_avelox_lbl.pdf