Sitafloxacin: Difference between revisions

From WikiMD's Wellness Encyclopedia

CSV import
 
CSV import
Line 1: Line 1:
'''Sitafloxacin''' is a [[fluoroquinolone]] [[antibiotic]] used in the treatment of various [[bacterial infections]]. It is particularly effective against [[gram-positive bacteria]] and [[gram-negative bacteria]], including those resistant to other fluoroquinolones.
{{Short description|An article about the antibiotic Sitafloxacin}}
{{Drugbox
| verifiedfields = changed
| verifiedrevid = 477002123
| image = Sitafloxacin.svg
| image_size = 200px
| image_alt = Chemical structure of Sitafloxacin
}}
 
'''Sitafloxacin''' is a [[fluoroquinolone]] [[antibiotic]] used in the treatment of various bacterial infections. It is known for its broad-spectrum activity against both [[Gram-positive bacteria|Gram-positive]] and [[Gram-negative bacteria|Gram-negative]] pathogens.


==Mechanism of Action==
==Mechanism of Action==
Sitafloxacin works by inhibiting the [[DNA gyrase]] and [[topoisomerase IV]], enzymes necessary for bacterial DNA replication, transcription, repair, and recombination. This inhibition results in the death of the bacteria, effectively treating the infection.
Sitafloxacin works by inhibiting bacterial [[DNA gyrase]] and [[topoisomerase IV]], enzymes critical for [[DNA replication]] and [[transcription (genetics)|transcription]]. This inhibition leads to the disruption of bacterial [[DNA synthesis]], ultimately resulting in bacterial cell death.


==Medical Uses==
==Pharmacokinetics==
Sitafloxacin is used to treat a variety of bacterial infections, including [[pneumonia]], [[urinary tract infections]], [[skin infections]], and [[intra-abdominal infections]]. It is also used in the treatment of [[tuberculosis]], particularly multi-drug resistant strains.
Sitafloxacin is well absorbed after oral administration, with a bioavailability of approximately 90%. It is widely distributed throughout the body, achieving therapeutic concentrations in various tissues and fluids. The drug is primarily excreted via the [[renal system]], with a half-life of approximately 5 to 7 hours.


==Side Effects==
==Clinical Uses==
Common side effects of sitafloxacin include [[nausea]], [[diarrhea]], [[headache]], and [[dizziness]]. More serious side effects can include [[tendon rupture]], [[QT prolongation]], and [[hypersensitivity reactions]].
Sitafloxacin is indicated for the treatment of a variety of infections, including:
* [[Respiratory tract infections]]
* [[Urinary tract infections]]
* [[Skin and soft tissue infections]]
* [[Gastrointestinal infections]]


==Drug Interactions==
==Adverse Effects==
Sitafloxacin can interact with other medications, including [[antacids]], [[iron supplements]], and [[multivitamins]]. These interactions can decrease the absorption of sitafloxacin, reducing its effectiveness.
Common adverse effects of sitafloxacin include [[nausea]], [[diarrhea]], and [[headache]]. Like other fluoroquinolones, it may also cause more serious side effects such as [[tendonitis]] and [[tendon rupture]], particularly in older adults and those on concurrent corticosteroid therapy.


==Precautions==
==Resistance==
Patients with a history of [[tendonitis]] or [[tendon rupture]] should use sitafloxacin with caution, as it can increase the risk of these conditions. Additionally, sitafloxacin should be used with caution in patients with a history of [[QT prolongation]] or other heart conditions.
Bacterial resistance to sitafloxacin can occur through mutations in the [[gyrA]] and [[parC]] genes, which encode the target enzymes DNA gyrase and topoisomerase IV, respectively. Efflux pumps and reduced permeability of the bacterial cell wall can also contribute to resistance.


==See Also==
==Related pages==
* [[Fluoroquinolone]]
* [[Fluoroquinolone]]
* [[Antibiotic resistance]]
* [[Antibiotic resistance]]
* [[DNA gyrase]]
* [[DNA gyrase]]
* [[Topoisomerase IV]]


[[Category:Fluoroquinolone antibiotics]]
[[Category:Antibiotics]]
[[Category:Antibiotics]]
[[Category:Fluoroquinolones]]
{{Antibiotics-stub}}
{{Medicine-stub}}

Revision as of 10:52, 15 February 2025

An article about the antibiotic Sitafloxacin


Sitafloxacin
INN
Drug class
Routes of administration
Pregnancy category
Bioavailability
Metabolism
Elimination half-life
Excretion
Legal status
CAS Number
PubChem
DrugBank
ChemSpider
KEGG


Sitafloxacin is a fluoroquinolone antibiotic used in the treatment of various bacterial infections. It is known for its broad-spectrum activity against both Gram-positive and Gram-negative pathogens.

Mechanism of Action

Sitafloxacin works by inhibiting bacterial DNA gyrase and topoisomerase IV, enzymes critical for DNA replication and transcription. This inhibition leads to the disruption of bacterial DNA synthesis, ultimately resulting in bacterial cell death.

Pharmacokinetics

Sitafloxacin is well absorbed after oral administration, with a bioavailability of approximately 90%. It is widely distributed throughout the body, achieving therapeutic concentrations in various tissues and fluids. The drug is primarily excreted via the renal system, with a half-life of approximately 5 to 7 hours.

Clinical Uses

Sitafloxacin is indicated for the treatment of a variety of infections, including:

Adverse Effects

Common adverse effects of sitafloxacin include nausea, diarrhea, and headache. Like other fluoroquinolones, it may also cause more serious side effects such as tendonitis and tendon rupture, particularly in older adults and those on concurrent corticosteroid therapy.

Resistance

Bacterial resistance to sitafloxacin can occur through mutations in the gyrA and parC genes, which encode the target enzymes DNA gyrase and topoisomerase IV, respectively. Efflux pumps and reduced permeability of the bacterial cell wall can also contribute to resistance.

Related pages