Ceftaroline Fosamil
Ceftaroline Fosamil Uses, Dosage, Side Effects, Food Interaction and all others data.
Ceftaroline Fosamil is a cephalosporin antibacterial indicated for the treatment of the following infections caused by designated susceptible bacteria:Acute bacterial skin and skin structure infections.Community-acquired bacterial pneumonia.
The time that unbound plasma concentration of ceftaroline exceeds the minimum inhibitory concentration (MIC) of the infecting organism has been shown to best correlate with efficacy in a neutropenic murine thigh infection model with S. aureus and S. pneumoniae.
No significant effect on QTc (corrected QT interval) interval was detected at peak plasma concentration or at any other time.
Trade Name | Ceftaroline Fosamil |
Generic | Ceftaroline fosamil |
Ceftaroline fosamil Other Names | Ceftarolina fosamilo, Ceftaroline, Ceftaroline fosamil, Ceftarolinum fosamilum |
Type | |
Formula | C22H21N8O8PS4 |
Weight | Average: 684.67 Monoisotopic: 684.010281362 |
Protein binding | approximately 20%. |
Groups | Approved, Investigational |
Therapeutic Class | |
Manufacturer | |
Available Country | |
Last Updated: | September 19, 2023 at 7:00 am |
Uses
Ceftaroline Fosamil is an antibacterial agent used to treat various bacterial infections, such as acute bacterial skin and skin structure infections and community-acquired bacterial pneumonia.
Ceftaroline Fosamil is indicated for the treatment of patients with the following infections caused by susceptible isolates of the designated microorganisms.
Ceftaroline Fosamil is also used to associated treatment for these conditions: Bacterial Infections, Community Acquired Pneumonia (CAP), Acute skin and subcutaneous tissue bacterial infections
How Ceftaroline Fosamil works
Ceftaroline Fosamil is an antibacterial drug.
Toxicity
LD50/LC50: Draize test, rabbit, eye: 100 mg/24H Moderate; Oral, mouse: LD50 = 300 mg/kg; Oral, rabbit: LD50 = 3200 mg/kg; Oral, rat: LD50 = 980 mg/kg.
Food Interaction
No interactions found.Volume of Distribution
Median 20.3 L (18.3-21.6 L).
Half Life
1.60 hours (600 mg dose).
Elimination Route
primarily eliminated by the kidneys (6% in feces within 48 hours).
Innovators Monograph
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