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'''| [[Ceftaroline overdosage|Overdosage]]'''
'''| [[Ceftaroline overdosage|Overdosage]]'''
'''| [[Ceftaroline dosage and administration|Dosage and Administration]]'''
'''| [[Ceftaroline dosage and administration|Dosage and Administration]]'''
'''| [[Ceftaroline compatibility and stability|Compatibility and Stability]]'''
'''| [[Ceftaroline clinical studies|Clinical Studies]]'''
'''| [[Ceftaroline how supplied|How Supplied]]'''
'''| [[Ceftaroline how supplied|How Supplied]]'''
'''| [[Ceftaroline labels and packages|Labels and Packages]]'''
'''| [[Ceftaroline labels and packages|Labels and Packages]]'''

Revision as of 08:25, 6 January 2014

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

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

Overview

Ceftaroline fosamil (INN) /sɛfˈtærɵliːn/, brand name Teflaro in the US and Zinforo in Europe, is an advanced-generation[1] cephalosporinantibiotic. It is active against methicillin-resistant Staphylococcus aureus (MRSA) and Gram-positive bacteria. It retains the activity of later-generation cephalosporins having broad-spectrum activity against Gram-negative bacteria. It is currently being investigated for community-acquired pneumonia[2] and complicated skin and skin structure infection.

Category

Cephalosporins, third generation.

US Brand Names

TEFLARO®


FDA Package Insert

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

References

http://www.accessdata.fda.gov/drugsatfda_docs/label/2011/200327s001lbl.pdf