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	<title>Cefroxadine - Revision history</title>
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	<updated>2026-04-25T02:24:48Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://wikimd.org/index.php?title=Cefroxadine&amp;diff=5627393&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
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		<updated>2024-04-19T10:47:41Z</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:Cefroxadine_synthesis.svg|Cefroxadine synthesis|thumb]]  &amp;#039;&amp;#039;&amp;#039;Cefroxadine&amp;#039;&amp;#039;&amp;#039; is a [[cephalosporin]] [[antibiotic]] used in the treatment of various bacterial infections. It belongs to the first generation of cephalosporins, which are a class of [[beta-lactam antibiotics]] similar in structure and mechanism of action to the [[penicillins]]. Cefroxadine works by inhibiting the synthesis of the bacterial cell wall, leading to cell death. It is effective against a wide range of gram-positive and some gram-negative bacteria, making it useful in treating conditions such as [[pharyngitis]], [[urinary tract infections]], and [[skin infections]].&lt;br /&gt;
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==Mechanism of Action==&lt;br /&gt;
Cefroxadine exerts its antibacterial effect by binding to specific penicillin-binding proteins (PBPs) located inside the bacterial cell wall. By inhibiting these PBPs, cefroxadine disrupts the final stages of bacterial cell wall synthesis, leading to cell lysis and death. This mechanism is similar to other beta-lactam antibiotics, which are known for their ability to target and disrupt the bacterial cell wall.&lt;br /&gt;
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==Pharmacokinetics==&lt;br /&gt;
The pharmacokinetics of cefroxadine involve its absorption, distribution, metabolism, and excretion. After oral administration, cefroxadine is well absorbed from the gastrointestinal tract. It is distributed throughout the body, including to the site of infection. The metabolism of cefroxadine is minimal, with the majority of the drug being excreted unchanged in the urine. This pharmacokinetic profile allows for effective concentrations of the drug to be maintained at the site of infection, ensuring its therapeutic efficacy.&lt;br /&gt;
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==Clinical Uses==&lt;br /&gt;
Cefroxadine is used to treat a variety of bacterial infections, including:&lt;br /&gt;
* [[Pharyngitis]] caused by Streptococcus species&lt;br /&gt;
* [[Urinary tract infections]] (UTIs) caused by Escherichia coli and other gram-negative bacteria&lt;br /&gt;
* [[Skin infections]] caused by Staphylococcus aureus and other gram-positive bacteria&lt;br /&gt;
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Its broad spectrum of activity against both gram-positive and some gram-negative bacteria makes it a versatile antibiotic for the treatment of these conditions.&lt;br /&gt;
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==Side Effects==&lt;br /&gt;
Like all antibiotics, cefroxadine can cause side effects. The most common side effects include:&lt;br /&gt;
* Gastrointestinal disturbances, such as nausea, vomiting, and diarrhea&lt;br /&gt;
* Allergic reactions, ranging from rash to more severe reactions like anaphylaxis&lt;br /&gt;
* Alterations in liver function tests&lt;br /&gt;
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Patients should be monitored for these side effects, and any severe or persistent symptoms should be reported to a healthcare provider.&lt;br /&gt;
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==Resistance==&lt;br /&gt;
Bacterial resistance to cefroxadine, as with other antibiotics, is a growing concern. Resistance mechanisms include the production of beta-lactamases, which can degrade the antibiotic, and alterations in the target PBPs, reducing the drug&amp;#039;s affinity for its target. Judicious use of cefroxadine and other antibiotics is essential to minimize the development of resistance.&lt;br /&gt;
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[[Category:Antibiotics]]&lt;br /&gt;
[[Category:Cephalosporin antibiotics]]&lt;br /&gt;
[[Category:Beta-lactam antibiotics]]&lt;br /&gt;
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		<author><name>Prab</name></author>
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