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	<id>https://wikimd.com/index.php?action=history&amp;feed=atom&amp;title=Azlocillin</id>
	<title>Azlocillin - Revision history</title>
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	<updated>2026-04-22T14:38:56Z</updated>
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		<id>https://wikimd.com/index.php?title=Azlocillin&amp;diff=5628804&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
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		<updated>2024-04-19T12:21:29Z</updated>

		<summary type="html">&lt;p&gt;CSV import&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;[[File:Azlocillin_synthesis.svg|Azlocillin synthesis|thumb]] [[File:Azlocillin_synthesis2.svg|Azlocillin synthesis2|thumb|left]]   &amp;#039;&amp;#039;&amp;#039;Azlocillin&amp;#039;&amp;#039;&amp;#039; is an [[antibiotic]] belonging to the class of [[penicillin]]s. It is a semi-synthetic compound that was developed to treat infections caused by [[Pseudomonas aeruginosa]] and other [[Gram-negative bacteria]]. Azlocillin works by inhibiting the synthesis of the bacterial [[cell wall]], leading to the death of the bacteria. This mechanism is similar to other penicillins but azlocillin has been specifically optimized for activity against certain resistant strains of bacteria.&lt;br /&gt;
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==Medical Uses==&lt;br /&gt;
Azlocillin is primarily used in the treatment of infections caused by Pseudomonas aeruginosa, a pathogen known for its resistance to many antibiotics and its association with hospital-acquired infections. These infections can include [[pneumonia]], [[urinary tract infections]] (UTIs), [[septicemia]], and infections in patients with [[cystic fibrosis]]. Due to its broad spectrum of activity, azlocillin may also be effective against infections caused by other Gram-negative organisms as well as some [[Gram-positive bacteria]].&lt;br /&gt;
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==Pharmacology==&lt;br /&gt;
The pharmacological action of azlocillin involves the inhibition of bacterial cell wall synthesis, a common mechanism among penicillin antibiotics. By binding to and inactivating specific penicillin-binding proteins (PBPs) on the bacterial cell wall, azlocillin prevents the cross-linking of peptidoglycan chains necessary for cell wall strength and rigidity. This action leads to cell lysis and the eventual death of the bacterium.&lt;br /&gt;
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Azlocillin is administered intravenously, as its bioavailability is poor when taken by mouth. It is distributed widely in the body, including in the [[pleural fluid]], [[ascites]], and [[cerebrospinal fluid]] (CSF), making it useful in treating infections in various body sites.&lt;br /&gt;
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==Side Effects==&lt;br /&gt;
Like other penicillins, azlocillin can cause a range of side effects. The most common include allergic reactions, which can range from mild [[rash]]es to severe [[anaphylaxis]]. Gastrointestinal disturbances such as [[nausea]], [[vomiting]], and [[diarrhea]] are also common. Less frequently, patients may experience changes in blood counts, including [[neutropenia]] and [[thrombocytopenia]], or liver enzyme elevations.&lt;br /&gt;
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==Resistance==&lt;br /&gt;
The emergence of bacterial resistance to azlocillin, as with other antibiotics, is a significant concern. Resistance mechanisms include the production of beta-lactamases that hydrolyze the antibiotic, alterations in the target PBPs, and changes in membrane permeability that reduce drug uptake. The use of azlocillin, like all antibiotics, should be guided by susceptibility testing to ensure effectiveness against the infecting organism and to help limit the development of resistance.&lt;br /&gt;
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==Conclusion==&lt;br /&gt;
Azlocillin is an important antibiotic in the treatment of infections caused by Pseudomonas aeruginosa and other resistant Gram-negative bacteria. Its role in combating hospital-acquired infections and infections in immunocompromised patients is particularly valuable. However, the emergence of resistance highlights the need for judicious use and ongoing research into new antimicrobial agents.&lt;br /&gt;
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[[Category:Antibiotics]]&lt;br /&gt;
[[Category:Penicillins]]&lt;br /&gt;
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{{medicine-stub}}&lt;/div&gt;</summary>
		<author><name>Prab</name></author>
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