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	<title>PG Blazer &#187; Pharmacology</title>
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	<description>Blaze your way towards a medical PG seat!</description>
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		<title>Online test series 6 &#8211; Pharmacology</title>
		<link>http://pgblazer.com/2011/06/online-test-series-6-pharmacology.html</link>
		<comments>http://pgblazer.com/2011/06/online-test-series-6-pharmacology.html#comments</comments>
		<pubDate>Wed, 08 Jun 2011 01:38:22 +0000</pubDate>
		<dc:creator>pgblazer</dc:creator>
				<category><![CDATA[Mock tests]]></category>
		<category><![CDATA[Pharmacology]]></category>

		<guid isPermaLink="false">http://pgblazer.com/?p=9795</guid>
		<description><![CDATA[
Questions summary:

All of the following are non selective beta blockers with additional actions except?
All of the following may be associated with beta 2 agonist treatment except?
True statement about clonidine are all except,
Finasteride is a:
Which of the following is not an alkylating agent?
Which of the following is a prodrug
All of the following are Gp IIb/Illa antagonist except?
Orange coloured urine is due to:
The drug having maximum propensity to cause peripheral neuropathy?
Nesiritide is a:

   
 
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                 Online test series 14 &#8211; Forensic Medicine</a>  
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			<content:encoded><![CDATA[<p><iframe name='proprofs' id='proprofs' height='601' width='540' frameborder=0 marginwidth=0 marginheight=0 src='http://www.proprofs.com/quiz-school/widget/v3/?id=241016&#038;bgcolor=ffffff&#038;fcolor=000000&#038;tcolor=000000&#038;w=520&#038;h=395&#038;ff=1&#038;fs=medium&#038;pplink=0&#038;socialmedia=0&#038;embedlink=0&#038;showpage=1&#038;btncolor=000000'></iframe></p>
<p>Questions summary:</p>
<ol>
<li>All of the following are non selective beta blockers with additional actions except?</li>
<li>All of the following may be associated with beta 2 agonist treatment except?</li>
<li>True statement about clonidine are all except,</li>
<li>Finasteride is a:</li>
<li>Which of the following is not an alkylating agent?</li>
<li>Which of the following is a prodrug</li>
<li>All of the following are Gp IIb/Illa antagonist except?</li>
<li>Orange coloured urine is due to:</li>
<li>The drug having maximum propensity to cause peripheral neuropathy?</li>
<li>Nesiritide is a:</li>
</ol>
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		<slash:comments>4</slash:comments>
		</item>
		<item>
		<title>Common poisonings and their management &#8211; Powerpoint presentation (ppt)</title>
		<link>http://pgblazer.com/2011/03/common-poisonings-and-their-management-powerpoint-presentation-ppt.html</link>
		<comments>http://pgblazer.com/2011/03/common-poisonings-and-their-management-powerpoint-presentation-ppt.html#comments</comments>
		<pubDate>Thu, 24 Mar 2011 11:35:22 +0000</pubDate>
		<dc:creator>pgblazer</dc:creator>
				<category><![CDATA[Pharmacology]]></category>
		<category><![CDATA[Powerpoint presentations]]></category>

		<guid isPermaLink="false">http://pgblazer.com/?p=5510</guid>
		<description><![CDATA[Powerpoint presentation summary:

General considerations

Statistics
Important things to remember


Aspirin

Indications
Clinical presentation in aspirin overdose
Complications
Management of salicylism


Paracetamol

Clinical presentation
Use of IV N-acetylcysteine


Carbon monoxide

Mechanism of hypoxia
Use of hyperbaric oxygen in management


Cocaine poisoning
Opiates
3,4-methylenedioxy-methamphetamine - MDMA (Ecstasy)

Author : Kevin O’Shaughnessy
 Download / View online
   
 
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			<content:encoded><![CDATA[<p>Powerpoint presentation summary:</p>
<ul>
<li>General considerations
<ul>
<li>Statistics</li>
<li>Important things to remember</li>
</ul>
</li>
<li>Aspirin
<ul>
<li>Indications</li>
<li>Clinical presentation in aspirin overdose</li>
<li>Complications</li>
<li>Management of salicylism</li>
</ul>
</li>
<li>Paracetamol
<ul>
<li>Clinical presentation</li>
<li>Use of IV N-acetylcysteine</li>
</ul>
</li>
<li>Carbon monoxide
<ul>
<li>Mechanism of hypoxia</li>
<li>Use of hyperbaric oxygen in management</li>
</ul>
</li>
<li>Cocaine poisoning</li>
<li>Opiates</li>
<li>3,4-methylenedioxy-methamphetamine - MDMA (Ecstasy)</li>
</ul>
<p>Author : Kevin O’Shaughnessy<br />
<a href="http://pgblazer.com/g2"> Download</a> / <a href="http://pgblazer.com/hh5">View online</a></p>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Anticoagulants, Antiplatelet drugs and Thrombolytic agents &#8211; Powerpoint presentation (ppt)</title>
		<link>http://pgblazer.com/2011/03/anticoagulants-antiplatelet-drugs-and-thrombolytic-agents-powerpoint-presentation-ppt.html</link>
		<comments>http://pgblazer.com/2011/03/anticoagulants-antiplatelet-drugs-and-thrombolytic-agents-powerpoint-presentation-ppt.html#comments</comments>
		<pubDate>Fri, 11 Mar 2011 08:32:23 +0000</pubDate>
		<dc:creator>pgblazer</dc:creator>
				<category><![CDATA[Pharmacology]]></category>
		<category><![CDATA[Powerpoint presentations]]></category>

		<guid isPermaLink="false">http://pgblazer.com/?p=5448</guid>
		<description><![CDATA[Anticoagulants, Antiplatelet drugs and Thrombolytic agents &#8211; Presentation Summary

Major classes of drugs
Platelet Activation
Aspirin
Newer antiplatelets &#8211; Thienopyridines
CAPRIE trial
CURE trial
MATCH trial
Glycoprotein IIb/IIIa antagonists
Fibrinogenesis
Heparin &#8211; Mechanism of action
Features of Low Molecular Weight Heparin
LMWH vs Unfractionated heparin
Warfarin
Pharmacokinetics of warfarin
Drugs interactions of Warfarin
Warfarin toxicity treatment
Fibrinolysis
Tissue plasminogen activator vs streptokinase
Beyond LMWH
Ximelagatran

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 ]]></description>
			<content:encoded><![CDATA[<p>Anticoagulants, Antiplatelet drugs and Thrombolytic agents &#8211; Presentation Summary</p>
<ul>
<li>Major classes of drugs</li>
<li>Platelet Activation</li>
<li>Aspirin</li>
<li>Newer antiplatelets &#8211; Thienopyridines</li>
<li>CAPRIE trial</li>
<li>CURE trial</li>
<li>MATCH trial</li>
<li>Glycoprotein IIb/IIIa antagonists</li>
<li>Fibrinogenesis</li>
<li>Heparin &#8211; Mechanism of action</li>
<li>Features of Low Molecular Weight Heparin</li>
<li>LMWH vs Unfractionated heparin</li>
<li>Warfarin</li>
<li>Pharmacokinetics of warfarin</li>
<li>Drugs interactions of Warfarin</li>
<li>Warfarin toxicity treatment</li>
<li>Fibrinolysis</li>
<li>Tissue plasminogen activator vs streptokinase</li>
<li>Beyond LMWH</li>
<li>Ximelagatran</li>
</ul>
<p><a href="http://pgblazer.com/380">Download</a> / <a href="http://pgblazer.com/s09">View online</a></p>
<div class="plus-one-wrap"><g:plusone size="medium" href="http://pgblazer.com/2011/03/anticoagulants-antiplatelet-drugs-and-thrombolytic-agents-powerpoint-presentation-ppt.html"></g:plusone></div>   
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		</item>
		<item>
		<title>Pharmacology of acute poisoning &#8211; Powerpoint presentation (ppt)</title>
		<link>http://pgblazer.com/2011/03/pharmacology-of-acute-poisoning-powerpoint-presentation-ppt.html</link>
		<comments>http://pgblazer.com/2011/03/pharmacology-of-acute-poisoning-powerpoint-presentation-ppt.html#comments</comments>
		<pubDate>Fri, 11 Mar 2011 01:20:35 +0000</pubDate>
		<dc:creator>pgblazer</dc:creator>
				<category><![CDATA[Pharmacology]]></category>
		<category><![CDATA[Powerpoint presentations]]></category>

		<guid isPermaLink="false">http://pgblazer.com/?p=5443</guid>
		<description><![CDATA[Pharmacology of acute poisoning &#8211; Powerpoint Summary

General considerations
History
Investigations
Management

Decreasing poison absorption
Increasing poison elimination


Paracetamol &#8211; overdose and management
Aspirin &#8211; overdose and management
Tri cyclic antidepressants - overdose and management
Benzodiazepine - overdose and management
Poisoning by other drugs

Author : Dr Ian Wilkinson
Download / View onl﻿ine
&#160;
   
 
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			<content:encoded><![CDATA[<p>Pharmacology of acute poisoning &#8211; Powerpoint Summary</p>
<ul>
<li>General considerations</li>
<li>History</li>
<li>Investigations</li>
<li>Management
<ul>
<li>Decreasing poison absorption</li>
<li>Increasing poison elimination</li>
</ul>
</li>
<li>Paracetamol &#8211; overdose and management</li>
<li>Aspirin &#8211; overdose and management</li>
<li>Tri cyclic antidepressants - overdose and management</li>
<li>Benzodiazepine - overdose and management</li>
<li>Poisoning by other drugs</li>
</ul>
<p>Author : Dr Ian Wilkinson</p>
<p><a href="http://pgblazer.com/ymx">Download</a> / <a href="http://docs.google.com/viewer?a=v&amp;q=cache:7_ZIi_SyBZ0J:www-clinpharm.medschl.cam.ac.uk/pages/teaching/course/overdose.ppt+http://www-clinpharm.medschl.cam.ac.uk/pages/teaching/course/overdose.ppt&amp;hl=en&amp;gl=in&amp;pid=bl&amp;srcid=ADGEESh5xk8GXDesvuMcu5MmeURtXISAnaQ8d4ZD2BljMwQM4mKVMx8HNugKRFch436t9VZ3KXhNJczcJTLM7kTxeYtVSkEq6wP_FhIE7tkvGlEAWpVyoz_E2bKrC0gJvApBmVsSQ02d&amp;sig=AHIEtbSSii_oBKsOXKfgSRTAXG9hy8Svzw">View onl﻿ine</a></p>
<p>&nbsp;</p>
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                 Common poisonings and their management &#8211; Powerpoint presentation (ppt)</a>  
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                 <a href="http://pgblazer.com/2011/01/acute-leukemia-powerpoint-presentation.html" rel="bookmark">  
                   
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                 Acute Leukemia &#8211; Powerpoint presentation</a>  
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                 Diabetes insipidus &#8211; Powerpoint presentation</a>  
             </li>  
   
           
     </ol>  
   
 ]]></content:encoded>
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		</item>
		<item>
		<title>Teriparatide &#8211; Mechanism of action</title>
		<link>http://pgblazer.com/2011/01/teriparatide-mechanism-of-action.html</link>
		<comments>http://pgblazer.com/2011/01/teriparatide-mechanism-of-action.html#comments</comments>
		<pubDate>Fri, 14 Jan 2011 01:29:04 +0000</pubDate>
		<dc:creator>pgblazer</dc:creator>
				<category><![CDATA[Pharmacology]]></category>

		<guid isPermaLink="false">http://pgblazer.com/?p=3830</guid>
		<description><![CDATA[
Teriparatide is a recombinant form of PTH that is used in patients with osteoporosis
The usual drugs used in osteoporosis are anti resorptive agents
But teriparatide has a unique mechanism of action
Endogenous PTH induces bone demineralisation
But intermittent pulses of exogenous PTH stimulates osteoblastic activity (Teriparatide is given once daily)
Teriparatide stimulates new bone formation &#8211; adds bone to periosteal surface and increases trabecular bone volume and connectivity

Reference:
Osteoporosis: a guide for clinicians By Pauline M. Camacho, Paul Miller

   
 
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 ]]></description>
			<content:encoded><![CDATA[<ul>
<li>Teriparatide is a recombinant form of PTH that is used in patients with osteoporosis</li>
<li>The usual drugs used in osteoporosis are anti resorptive agents</li>
<li>But teriparatide has a unique mechanism of action</li>
<li>Endogenous PTH induces bone demineralisation</li>
<li>But intermittent pulses of exogenous PTH stimulates osteoblastic activity (Teriparatide is given once daily)</li>
<li>Teriparatide stimulates new bone formation &#8211; adds bone to periosteal surface and increases trabecular bone volume and connectivity</li>
</ul>
<p>Reference:<br />
<a href="http://pgblazer.com/x64">Osteoporosis: a guide for clinicians By Pauline M. Camacho, Paul Miller<br />
</a></p>
<div class="plus-one-wrap"><g:plusone size="medium" href="http://pgblazer.com/2011/01/teriparatide-mechanism-of-action.html"></g:plusone></div>   
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                 Microbiology &#8211; MCQ 41 &#8211; Mechanism of action of cholera toxin</a>  
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		<item>
		<title>Adverse effects of thalidomide</title>
		<link>http://pgblazer.com/2011/01/adverse-effects-of-thalidomide.html</link>
		<comments>http://pgblazer.com/2011/01/adverse-effects-of-thalidomide.html#comments</comments>
		<pubDate>Thu, 13 Jan 2011 12:41:10 +0000</pubDate>
		<dc:creator>pgblazer</dc:creator>
				<category><![CDATA[Pharmacology]]></category>

		<guid isPermaLink="false">http://pgblazer.com/?p=3799</guid>
		<description><![CDATA[The most important adverse effect of thalidomide is teratogenicity. The others include:

Peripheral neuropathy
Deep vein thrombosis
Constipation
Rash
Fatigue
Hypothyroidism

Reference:
Basic and Clinical Pharmacology, Katzung, 10th edition, p919
   
 
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 ]]></description>
			<content:encoded><![CDATA[<p>The most important adverse effect of thalidomide is teratogenicity. The others include:</p>
<ul>
<li>Peripheral neuropathy</li>
<li>Deep vein thrombosis</li>
<li>Constipation</li>
<li>Rash</li>
<li>Fatigue</li>
<li>Hypothyroidism</li>
</ul>
<p>Reference:<br />
Basic and Clinical Pharmacology, Katzung, 10th edition, p919</p>
<div class="plus-one-wrap"><g:plusone size="medium" href="http://pgblazer.com/2011/01/adverse-effects-of-thalidomide.html"></g:plusone></div>   
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                 Pharmacology &#8211; MCQ 123 &#8211; Side effects of amiodarone</a>  
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		<item>
		<title>Drug interactions of lithium</title>
		<link>http://pgblazer.com/2011/01/drug-interactions-of-lithium.html</link>
		<comments>http://pgblazer.com/2011/01/drug-interactions-of-lithium.html#comments</comments>
		<pubDate>Thu, 13 Jan 2011 11:55:37 +0000</pubDate>
		<dc:creator>pgblazer</dc:creator>
				<category><![CDATA[Pharmacology]]></category>

		<guid isPermaLink="false">http://pgblazer.com/?p=3794</guid>
		<description><![CDATA[
Renal clearance of lithium is decreased by about 25% in those who take diuretics, hence dosage should be adjusted
Similar effect is also noted in certain newer NSAID&#8217;s
Neuroleptics (other than clozapine and newer antipsychotics) when given with lithium produce increased extra pyramidal side effects

Reference:
Basic and Clinical Pharmacology, Katzung, 10th edition, p471
   
 
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			<content:encoded><![CDATA[<ul>
<li>Renal clearance of lithium is decreased by about 25% in those who take diuretics, hence dosage should be adjusted</li>
<li>Similar effect is also noted in certain newer NSAID&#8217;s</li>
<li>Neuroleptics (other than clozapine and newer antipsychotics) when given with lithium produce increased extra pyramidal side effects</li>
</ul>
<p>Reference:<br />
Basic and Clinical Pharmacology, Katzung, 10th edition, p471</p>
<div class="plus-one-wrap"><g:plusone size="medium" href="http://pgblazer.com/2011/01/drug-interactions-of-lithium.html"></g:plusone></div>   
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		<title>SERCA &#8211; Acronym</title>
		<link>http://pgblazer.com/2010/10/serca-acronym.html</link>
		<comments>http://pgblazer.com/2010/10/serca-acronym.html#comments</comments>
		<pubDate>Thu, 28 Oct 2010 00:45:13 +0000</pubDate>
		<dc:creator>pgblazer</dc:creator>
				<category><![CDATA[Acronyms]]></category>
		<category><![CDATA[Pharmacology]]></category>

		<guid isPermaLink="false">http://pgblazer.com/?p=3359</guid>
		<description><![CDATA[
SERCA stands for:

Smooth Endoplasmic Reticulum Calcium Aptase (involved in sequestration of calcium for later release)


   
 
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     </ol>  
   
 ]]></description>
			<content:encoded><![CDATA[<div>
<p>SERCA stands for:</p>
<ul>
<li>Smooth Endoplasmic Reticulum Calcium Aptase (involved in sequestration of calcium for later release)</li>
</ul>
</div>
<div class="plus-one-wrap"><g:plusone size="medium" href="http://pgblazer.com/2010/10/serca-acronym.html"></g:plusone></div>   
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		<title>Ten classes of antidiabetic drugs</title>
		<link>http://pgblazer.com/2010/04/ten-classes-of-antidiabetic-drugs.html</link>
		<comments>http://pgblazer.com/2010/04/ten-classes-of-antidiabetic-drugs.html#comments</comments>
		<pubDate>Tue, 27 Apr 2010 01:55:41 +0000</pubDate>
		<dc:creator>admin2</dc:creator>
				<category><![CDATA[Medicine]]></category>
		<category><![CDATA[Pharmacology]]></category>

		<guid isPermaLink="false">http://www.pgblazer.com/?p=1741</guid>
		<description><![CDATA[Ten classes of antidiabetic drugs:
1. Biguanides: e.g. Metformin
2. Glinides: e.g. Repaglinide, Nateglinide
3. Sulfonylureas: e.g. Glibenclamide, Glimiperide
4. Alpha-glucosidase inhibitors: Acarbose, Voglibose
5. Thiazolidinediones: e.g. Rosiglitazone, Pioglitazone
6. Incretin mimetics (glucagon-like peptide-1 mimetics): Exenatide
7. Dipeptidyl peptidase-IV inhibitors (DPP-IV): Sitagliptin
8. Amylin analogs: e.g. Pramlintide
9. Bile acid sequestrants: e.g. Colesevelam
10. Insulin
   
 
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                 AIIMS May 2011 &#8211; MCQ 63</a>  
             </li>  
   
           
     </ol>  
   
 ]]></description>
			<content:encoded><![CDATA[<p>Ten classes of antidiabetic drugs:</p>
<p>1. Biguanides: e.g. Metformin<br />
2. Glinides: e.g. Repaglinide, Nateglinide<br />
3. Sulfonylureas: e.g. Glibenclamide, Glimiperide<br />
4. Alpha-glucosidase inhibitors: Acarbose, Voglibose<br />
5. Thiazolidinediones: e.g. Rosiglitazone, Pioglitazone<br />
6. Incretin mimetics (glucagon-like peptide-1 mimetics): Exenatide<br />
7. Dipeptidyl peptidase-IV inhibitors (DPP-IV): Sitagliptin<br />
8. Amylin analogs: e.g. Pramlintide<br />
9. Bile acid sequestrants: e.g. Colesevelam<br />
10. Insulin</p>
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		<title>Alfuzosin</title>
		<link>http://pgblazer.com/2010/03/alfuzosin.html</link>
		<comments>http://pgblazer.com/2010/03/alfuzosin.html#comments</comments>
		<pubDate>Mon, 15 Mar 2010 16:24:31 +0000</pubDate>
		<dc:creator>pgblazer</dc:creator>
				<category><![CDATA[Pharmacology]]></category>
		<category><![CDATA[Alfuzosin]]></category>
		<category><![CDATA[alpha 1 receptor antagonist]]></category>
		<category><![CDATA[Benign Prostatic Hyperplasia]]></category>
		<category><![CDATA[bhp]]></category>
		<category><![CDATA[bph]]></category>

		<guid isPermaLink="false">http://www.pgblazer.com/?p=1672</guid>
		<description><![CDATA[
It is an alpha 1 receptor antagonist
Used in treatment of Benign Prostatic Hyperplasia (BPH)

   
 
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			<content:encoded><![CDATA[<ul>
<li>It is an alpha 1 receptor antagonist</li>
<li>Used in treatment of Benign Prostatic Hyperplasia (BPH)</li>
</ul>
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		<title>Lipotropic factor</title>
		<link>http://pgblazer.com/2009/11/lipotropic-factor.html</link>
		<comments>http://pgblazer.com/2009/11/lipotropic-factor.html#comments</comments>
		<pubDate>Mon, 02 Nov 2009 10:39:27 +0000</pubDate>
		<dc:creator>pgblazer</dc:creator>
				<category><![CDATA[Medicine]]></category>
		<category><![CDATA[Pharmacology]]></category>

		<guid isPermaLink="false">http://www.pgblazer.com/?p=1423</guid>
		<description><![CDATA[Substance which prevents excess accumulation of fat in the liver.
e.g.: choline, lipocaic, inositol
   
 
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			<content:encoded><![CDATA[<p>Substance which prevents excess accumulation of fat in the liver.</p>
<p>e.g.: choline, lipocaic, inositol</p>
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		<title>Liquorice &#8211; pharyngeal demulcent</title>
		<link>http://pgblazer.com/2009/10/liquorice-pharyngeal-demulcent.html</link>
		<comments>http://pgblazer.com/2009/10/liquorice-pharyngeal-demulcent.html#comments</comments>
		<pubDate>Thu, 15 Oct 2009 08:02:22 +0000</pubDate>
		<dc:creator>pgblazer</dc:creator>
				<category><![CDATA[Pharmacology]]></category>

		<guid isPermaLink="false">http://www.pgblazer.com/?p=1417</guid>
		<description><![CDATA[Root of Glycyrrhiza glabra. (from the Greek γλυκύρριζα or γλυκόριζα meaning &#8220;sweet root&#8220;)

-used as pharyngeal demulcent
-also used in confectionaries
   
 
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			<content:encoded><![CDATA[<p style="margin: 0in; font-family: Calibri; font-size: 11.0pt;"><span style="color: black;">Root of </span><span style="font-style: italic; color: black;">Glycyrrhiza glabra.</span><span style="color: black;"> (from the Greek </span><span style="font-style: italic; color: black;">γλυκύρριζα</span><span style="color: black;"> or </span><span style="font-style: italic; color: black;">γλυκόριζα</span><span style="color: black;"> meaning &#8220;<strong>sweet root</strong>&#8220;)</span></p>
<p style="margin: 0in; font-family: Tahoma; font-size: 8.0pt; color: #666666;">
<p style="margin: 0in; font-family: Calibri; font-size: 11.0pt;">-used as <span style="font-weight: bold;">pharyngeal demulcent</span></p>
<p style="margin: 0in; font-family: Calibri; font-size: 11.0pt;">-also used in confectionaries</p>
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		<title>Normal Saline</title>
		<link>http://pgblazer.com/2009/09/normal-saline.html</link>
		<comments>http://pgblazer.com/2009/09/normal-saline.html#comments</comments>
		<pubDate>Sun, 06 Sep 2009 09:58:43 +0000</pubDate>
		<dc:creator>admin2</dc:creator>
				<category><![CDATA[Biochemistry]]></category>
		<category><![CDATA[Pharmacology]]></category>

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		<description><![CDATA[Normal Saline: 9 gram of NaCl in 1 litre of water
Definition
   
 
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			<content:encoded><![CDATA[<p>Normal Saline: 9 gram of NaCl in 1 litre of water</p>
<p>Definition</p>
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		<title>DMPS &#8211; Acronym</title>
		<link>http://pgblazer.com/2009/07/dmps-acronym.html</link>
		<comments>http://pgblazer.com/2009/07/dmps-acronym.html#comments</comments>
		<pubDate>Thu, 16 Jul 2009 03:39:09 +0000</pubDate>
		<dc:creator>pgblazer</dc:creator>
				<category><![CDATA[Acronyms]]></category>
		<category><![CDATA[Pharmacology]]></category>

		<guid isPermaLink="false">http://www.pgblazer.com/?p=1375</guid>
		<description><![CDATA[DMPS &#8211; Dimercaptopropane sulfonate. Used as a chelating agent for treatment of heavy metal poisoning.
   
 
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alt="Dimercaprol &#8211; British anti lewisite (BAL)" class="left" width="100px" height="100px"  />
                   
   
                 Dimercaprol &#8211; British anti lewisite (BAL)</a>  
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                 Forensic medicine &#8211; MCQ 14 &#8211; Preservation of brain</a>  
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                 <a href="http://pgblazer.com/2009/02/dots.html" rel="bookmark">  
                   
                     <img src="http://d36i1lch6ipbwf.cloudfront.net/wp-content/themes/arthemia/default-image.jpg" alt="DOTS &#8211; Acronym" width="100px" height="100px"  />  
                   
   
                 DOTS &#8211; Acronym</a>  
             </li>  
   
           
     </ol>  
   
 ]]></description>
			<content:encoded><![CDATA[<p>DMPS &#8211; Dimercaptopropane sulfonate. Used as a chelating agent for treatment of heavy metal poisoning.</p>
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		<title>Adverse effects of ciprofloxacin</title>
		<link>http://pgblazer.com/2009/06/adverse-effects-of-ciprofloxacin.html</link>
		<comments>http://pgblazer.com/2009/06/adverse-effects-of-ciprofloxacin.html#comments</comments>
		<pubDate>Sat, 13 Jun 2009 02:35:39 +0000</pubDate>
		<dc:creator>admin2</dc:creator>
				<category><![CDATA[Pharmacology]]></category>

		<guid isPermaLink="false">http://www.pgblazer.com/?p=1286</guid>
		<description><![CDATA[Nausea, bad taste in mouth, vomiting
Inability to concentrate, tremors, seizures
Head ache, dizziness, rashes, photophobia
Swelling of lips, tendonitis, tendon rupture
Seizures are more likely if ciprofloxacin is combined with theophylline because theophylline increases the blood levels of ciprofloxacin.
   
 
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			<content:encoded><![CDATA[<p>Nausea, bad taste in mouth, vomiting</p>
<p>Inability to concentrate, tremors, seizures</p>
<p>Head ache, dizziness, rashes, photophobia</p>
<p>Swelling of lips, tendonitis, tendon rupture</p>
<p>Seizures are more likely if ciprofloxacin is combined with theophylline because theophylline increases the blood levels of ciprofloxacin.</p>
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		<title>Rationale for multi-drug therapy in tuberculosis</title>
		<link>http://pgblazer.com/2009/06/rationale-for-multi-drug-therapy-in-tuberculosis.html</link>
		<comments>http://pgblazer.com/2009/06/rationale-for-multi-drug-therapy-in-tuberculosis.html#comments</comments>
		<pubDate>Sat, 13 Jun 2009 02:32:08 +0000</pubDate>
		<dc:creator>admin2</dc:creator>
				<category><![CDATA[Pharmacology]]></category>

		<guid isPermaLink="false">http://www.pgblazer.com/?p=1284</guid>
		<description><![CDATA[If a single drug is given for the treatment of tuberculosis, there is increased chance of development of resistance to the drug. The incidence of resistant strain in an individual will be about 1 in 10^6  to 10^8. But an indiviual be infected with 10^10 to 10^12 organisms. So if a single drug is given, the number of remaining organisms will be too high for the immune system to remove them. The probability of an organizm resistance to the drug is independant of the probability to develop resistance to other ...   
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			<content:encoded><![CDATA[<p>If a single drug is given for the treatment of tuberculosis, there is increased chance of development of resistance to the drug. The incidence of resistant strain in an individual will be about 1 in 10^6  to 10^8. But an indiviual be infected with 10^10 to 10^12 organisms. So if a single drug is given, the number of remaining organisms will be too high for the immune system to remove them. The probability of an organizm resistance to the drug is independant of the probability to develop resistance to other drugs. Hence when two drugs are combined, the probability of resistance will be about 1 in 10^12 or less. The remaining organisms can be easily removed by the immune systems. This is the rationale for multi-drug therapy in tuberculosis.</p>
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		<title>Dimercaprol &#8211; British anti lewisite (BAL)</title>
		<link>http://pgblazer.com/2009/06/dimercaprol-british-anti-lewisite-bal.html</link>
		<comments>http://pgblazer.com/2009/06/dimercaprol-british-anti-lewisite-bal.html#comments</comments>
		<pubDate>Sat, 13 Jun 2009 02:24:13 +0000</pubDate>
		<dc:creator>admin2</dc:creator>
				<category><![CDATA[Pharmacology]]></category>

		<guid isPermaLink="false">http://www.pgblazer.com/?p=1282</guid>
		<description><![CDATA[Dimercaprol, also known as British anti lewisite (BAL) is a chelating agent used in the treatment of heavy metal poising (those which act by inhibiting the SH group containing enzymes). It has two SH (sulfhydryl) groups which can bind to these atoms. It can form 1:1 or 2:1 complex with metals, 2:1 being more stable. It can be used used in the treatment of poisoning by arsenic, antimony, bismuth, copper and gold. Dimercaprol is used along with penicillamine in the treatment of lead poisoning and also in the treatment of Wilson&#8217;s ...   
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			<content:encoded><![CDATA[<p>Dimercaprol, also known as British anti lewisite (BAL) is a chelating agent used in the treatment of heavy metal poising (those which act by inhibiting the SH group containing enzymes). It has two SH (sulfhydryl) groups which can bind to these atoms. It can form 1:1 or 2:1 complex with metals, 2:1 being more stable. It can be used used in the treatment of poisoning by arsenic, antimony, bismuth, copper and gold. Dimercaprol is used along with penicillamine in the treatment of lead poisoning and also in the treatment of Wilson&#8217;s disease.</p>
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		<title>Leuprolide and flutamide</title>
		<link>http://pgblazer.com/2009/06/leuprolide-and-flutamide.html</link>
		<comments>http://pgblazer.com/2009/06/leuprolide-and-flutamide.html#comments</comments>
		<pubDate>Sat, 13 Jun 2009 02:17:01 +0000</pubDate>
		<dc:creator>admin2</dc:creator>
				<category><![CDATA[Pharmacology]]></category>

		<guid isPermaLink="false">http://www.pgblazer.com/?p=1280</guid>
		<description><![CDATA[Leuprolide is a superactive GnRH (Gonadotropin releasing hormone) agonist. It can be given with flutamide for prostate cancer. Gonadotropin secretion occurs due to pulsatile secretion of GnRH. But when a long acting GnRH agonist like leuprolide is given, initially there is an increased release of gonadotropins, but soon there is downregulation of GnRH receptors and the release is prevented. This action can be utilized in the treatment of prostatic cancer which is a hormone dependant tumour. But the initial increase in the release of gonadotropins can cause a flaring up of the ...   
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			<content:encoded><![CDATA[<p>Leuprolide is a superactive GnRH (Gonadotropin releasing hormone) agonist. It can be given with flutamide for prostate cancer. Gonadotropin secretion occurs due to pulsatile secretion of GnRH. But when a long acting GnRH agonist like leuprolide is given, initially there is an increased release of gonadotropins, but soon there is downregulation of GnRH receptors and the release is prevented. This action can be utilized in the treatment of prostatic cancer which is a hormone dependant tumour. But the initial increase in the release of gonadotropins can cause a flaring up of the tumour. This can be prevented by concurrent administration of an anti-androgen such as flutamide.</p>
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		<title>Ethinyl estradiol and norgestrel</title>
		<link>http://pgblazer.com/2009/06/ethinyl-estradiol-and-norgestrel.html</link>
		<comments>http://pgblazer.com/2009/06/ethinyl-estradiol-and-norgestrel.html#comments</comments>
		<pubDate>Sat, 13 Jun 2009 02:10:35 +0000</pubDate>
		<dc:creator>admin2</dc:creator>
				<category><![CDATA[Pharmacology]]></category>

		<guid isPermaLink="false">http://www.pgblazer.com/?p=1276</guid>
		<description><![CDATA[Ethinyl estradiol and norgestrel are a combination of drugs used as hormonal contraceptive in women. Ethinyl estradiol is synthetic estrogen analogue and norgestrel is a synthetic progesterone analogue.
Mechanism of action
Ethinyl estradiol and norgestrel cause feed back inhibition of GNRH (Gonadotropin releasing hormone), FSH (follicle stimulating hormone) and LH (leutinizing hormone). Thus the mid cycle LH surge is prevented and ovulation does not occur. Progesterone makes the cervical mucus thick and impenetrable to sperms. The tubal and uterine motility is affected in such a way as to prevent fertilisation. Even if ovulation and fertilization ...   
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			<content:encoded><![CDATA[<p>Ethinyl estradiol and norgestrel are a combination of drugs used as hormonal contraceptive in women. Ethinyl estradiol is synthetic estrogen analogue and norgestrel is a synthetic progesterone analogue.</p>
<p><strong>Mechanism of action</strong></p>
<p>Ethinyl estradiol and norgestrel cause feed back inhibition of GNRH (Gonadotropin releasing hormone), FSH (follicle stimulating hormone) and LH (leutinizing hormone). Thus the mid cycle LH surge is prevented and ovulation does not occur. Progesterone makes the cervical mucus thick and impenetrable to sperms. The tubal and uterine motility is affected in such a way as to prevent fertilisation. Even if ovulation and fertilization occurs, the endometrium will be out of phase with the fertilization and implantation does not occur. The addition of progesterone ensures that the bleeding will occur after the cycle so that continuous endometrial proliferation and potential for endometrial carcinoma by estrogenic stimulation is prevented.</p>
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		<title>Linezolid</title>
		<link>http://pgblazer.com/2009/06/linezolid.html</link>
		<comments>http://pgblazer.com/2009/06/linezolid.html#comments</comments>
		<pubDate>Fri, 12 Jun 2009 01:59:35 +0000</pubDate>
		<dc:creator>admin2</dc:creator>
				<category><![CDATA[Pharmacology]]></category>

		<guid isPermaLink="false">http://www.pgblazer.com/?p=1274</guid>
		<description><![CDATA[Linezolid is an oxazolidinone antimicrobial agent. It is a bacteriostatic agent.
Spectrum of action
MRSA (Methicillin resistant Staphylococcus areus), some VRSA (Vancomycin resistant Staphylococcus areus), VRE (Vancomycin resistant enterococci), Streptococcus pyogenes, S. viridans, S. pneumoniae, Clostridia, Mycobacterium tuberculosis, Listeria.
Mechanism of action
It binds to the 23S fraction of the 50S subunit of the bacterial ribosome. It prevents the formation of N-formyl methionine tRNA &#8211; 70S ribosome complex, thus preventing protein synthesis. Since the drug has a different site of action, it does not have cross resistance with other antimicrobial agents.
Pharmacokinetics
It is well absorbed orally.
Uses
Linezolid should ...   
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			<content:encoded><![CDATA[<p>Linezolid is an oxazolidinone antimicrobial agent. It is a bacteriostatic agent.</p>
<p><strong>Spectrum of action</strong></p>
<p>MRSA (Methicillin resistant Staphylococcus areus), some VRSA (Vancomycin resistant Staphylococcus areus), VRE (Vancomycin resistant enterococci), Streptococcus pyogenes, S. viridans, S. pneumoniae, Clostridia, Mycobacterium tuberculosis, Listeria.</p>
<p><strong>Mechanism of action</strong></p>
<p>It binds to the 23S fraction of the 50S subunit of the bacterial ribosome. It prevents the formation of N-formyl methionine tRNA &#8211; 70S ribosome complex, thus preventing protein synthesis. Since the drug has a different site of action, it does not have cross resistance with other antimicrobial agents.</p>
<p><strong>Pharmacokinetics</strong></p>
<p>It is well absorbed orally.</p>
<p><strong>Uses</strong></p>
<p>Linezolid should not be used for simple infections to prevent development of resistance. It is used for severe hospital acquired pneumonias, wound infections by MRSA, VRSA, and in febrile neutropenia.</p>
<p><em><strong>It is not useful for treatment of enterococcal bacterial endocarditis as it is only bacteriostatic.</strong></em></p>
<p><strong>Dosage</strong></p>
<p>600 mg twice daily, oral or intravenous.</p>
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		<title>Urinary antiseptics</title>
		<link>http://pgblazer.com/2009/06/urinary-antiseptics.html</link>
		<comments>http://pgblazer.com/2009/06/urinary-antiseptics.html#comments</comments>
		<pubDate>Thu, 11 Jun 2009 02:12:31 +0000</pubDate>
		<dc:creator>admin2</dc:creator>
				<category><![CDATA[Pharmacology]]></category>

		<guid isPermaLink="false">http://www.pgblazer.com/?p=1271</guid>
		<description><![CDATA[Urinary antiseptics are antimicrobial agents. When these are given in orally tolerated doses, they attain antibacterial concentrations only in urine due to concentration in the renal tubules. These can be given for lower urinary tract infections, but are not suitable for upper urinary tract infections. eg: nitrofurantoin, methenamine.
   
 
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			<content:encoded><![CDATA[<p>Urinary antiseptics are antimicrobial agents. When these are given in orally tolerated doses, they attain antibacterial concentrations only in urine due to concentration in the renal tubules. These can be given for lower urinary tract infections, but are not suitable for upper urinary tract infections. eg: nitrofurantoin, methenamine.</p>
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		<title>Isoniazid and pyridoxine</title>
		<link>http://pgblazer.com/2009/06/isoniazid-and-pyridoxine.html</link>
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		<pubDate>Thu, 11 Jun 2009 02:07:49 +0000</pubDate>
		<dc:creator>admin2</dc:creator>
				<category><![CDATA[Pharmacology]]></category>

		<guid isPermaLink="false">http://www.pgblazer.com/?p=1269</guid>
		<description><![CDATA[Isoniazid is an antituberculous drug. It can cause peripheral neuropathy and rarely convulsions by decreasing the availability of pyridoxine (vitamin B6). Isoniazid binds to pyridoxal-5-phosphate, the active form of pyridoxine to form isoniazid-pyridoxal hydrazone. Pyridoxal-5-phosphate is necessary for the functioning of the enzymes glutamic acid decarboxylase and GABA transaminase which function in the GABA synthesis pathway. Thus isoniazid decreases the synthesis of GABA. Since GABA is an inhibitory neurotransmitter, deficiency of GABA can lead to increased excitatory action and siezures.
Pyridoxine 10 mg per day can be used to prevent peripheral ...   
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			<content:encoded><![CDATA[<p>Isoniazid is an antituberculous drug. It can cause peripheral neuropathy and rarely convulsions by decreasing the availability of pyridoxine (vitamin B6). Isoniazid binds to pyridoxal-5-phosphate, the active form of pyridoxine to form isoniazid-pyridoxal hydrazone. Pyridoxal-5-phosphate is necessary for the functioning of the enzymes glutamic acid decarboxylase and GABA transaminase which function in the GABA synthesis pathway. Thus isoniazid decreases the synthesis of GABA. Since GABA is an inhibitory neurotransmitter, deficiency of GABA can lead to increased excitatory action and siezures.</p>
<p>Pyridoxine 10 mg per day can be used to prevent peripheral neuropathy. In established isoniazid induced peripheral neuropathy, pyridoxine 100 mg per day is given.</p>
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		<title>Amoxycillin and clavulanic acid (Co-amoxyclav)</title>
		<link>http://pgblazer.com/2009/06/amoxycillin-and-clavulanic-acid.html</link>
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		<pubDate>Thu, 11 Jun 2009 01:59:08 +0000</pubDate>
		<dc:creator>admin2</dc:creator>
				<category><![CDATA[Pharmacology]]></category>

		<guid isPermaLink="false">http://www.pgblazer.com/?p=1266</guid>
		<description><![CDATA[Amoxycillin is an extended spectrum aminopenicillin. But it is not active against penicillinase producing organism. Clavulanic acid is a penicillinase inhibitor which initially reversibly and then irreversibly inhibits penicillinase 2-5 except cephalosporinase. So this drug combination has a synergistic action.
   
 
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			<content:encoded><![CDATA[<p>Amoxycillin is an extended spectrum aminopenicillin. But it is not active against penicillinase producing organism. Clavulanic acid is a penicillinase inhibitor which initially reversibly and then irreversibly inhibits penicillinase 2-5 except cephalosporinase. So this drug combination has a synergistic action.</p>
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		<item>
		<title>Classification of oral hypoglycemic agents</title>
		<link>http://pgblazer.com/2009/06/classification-of-oral-hypoglycemic-agents.html</link>
		<comments>http://pgblazer.com/2009/06/classification-of-oral-hypoglycemic-agents.html#comments</comments>
		<pubDate>Thu, 11 Jun 2009 01:55:03 +0000</pubDate>
		<dc:creator>admin2</dc:creator>
				<category><![CDATA[Pharmacology]]></category>

		<guid isPermaLink="false">http://www.pgblazer.com/?p=1262</guid>
		<description><![CDATA[
Sulphonyl ureas &#8211; first generation (tolbutamide, chlorpropamide); second generation &#8211; (glibenglamide, glipizide, gliclazide, glimiperide)
Biguanides &#8211; metformin
Meglitinides &#8211; repaglinide, nateglinide
Thiazolidine diones &#8211; rosiglitazone, pioglitazone
Alpha glucosidase inhibitors &#8211; acarbose, miglitol
 Dipeptidyl peptidase-4 (DPP-4) inhibitors &#8211; sitagliptin
Glucagon like peptide (GLP-1) analogue &#8211; exenatide

   
 
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			<content:encoded><![CDATA[<ol>
<li>Sulphonyl ureas &#8211; first generation (tolbutamide, chlorpropamide); second generation &#8211; (glibenglamide, glipizide, gliclazide, glimiperide)</li>
<li>Biguanides &#8211; metformin</li>
<li>Meglitinides &#8211; repaglinide, nateglinide</li>
<li>Thiazolidine diones &#8211; rosiglitazone, pioglitazone</li>
<li>Alpha glucosidase inhibitors &#8211; acarbose, miglitol</li>
<li> Dipeptidyl peptidase-4 (DPP-4) inhibitors &#8211; sitagliptin</li>
<li>Glucagon like peptide (GLP-1) analogue &#8211; exenatide</li>
</ol>
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		<title>Glibenclamide</title>
		<link>http://pgblazer.com/2009/06/glibenclamide.html</link>
		<comments>http://pgblazer.com/2009/06/glibenclamide.html#comments</comments>
		<pubDate>Wed, 10 Jun 2009 15:39:40 +0000</pubDate>
		<dc:creator>admin2</dc:creator>
				<category><![CDATA[Pharmacology]]></category>

		<guid isPermaLink="false">http://www.pgblazer.com/?p=1260</guid>
		<description><![CDATA[Glibenclamide is an oral hypoglycemic drug belonging to the group sulphonyl ureas. It is a second generation sulphonyl urea. Other sulphonyl ureas include &#8211; glipizide, gliclazide and glimiperide.
Mechanism of action
It acts by increasing the release of insulin from the pancreatic beta cells. Glibenclamide acts by binding to sulphonyl urea receptor of the ATP sensitive potassium channel in the pancreatic beta cells. This reduces conductivity of the channel, which causes depolarisation of the pancreatic beta cells, resulting in the opening of voltage sensitive calcium channels. Opening of the channels cause calcium ...   
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			<content:encoded><![CDATA[<p>Glibenclamide is an oral hypoglycemic drug belonging to the group sulphonyl ureas. It is a second generation sulphonyl urea. Other sulphonyl ureas include &#8211; glipizide, gliclazide and glimiperide.</p>
<p><strong>Mechanism of action</strong></p>
<p>It acts by increasing the release of insulin from the pancreatic beta cells. Glibenclamide acts by binding to sulphonyl urea receptor of the ATP sensitive potassium channel in the pancreatic beta cells. This reduces conductivity of the channel, which causes depolarisation of the pancreatic beta cells, resulting in the opening of voltage sensitive calcium channels. Opening of the channels cause calcium influx which leads to release of insulin.</p>
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		<title>Albenadazole</title>
		<link>http://pgblazer.com/2009/06/albenadazole.html</link>
		<comments>http://pgblazer.com/2009/06/albenadazole.html#comments</comments>
		<pubDate>Wed, 10 Jun 2009 15:32:21 +0000</pubDate>
		<dc:creator>admin2</dc:creator>
				<category><![CDATA[Pharmacology]]></category>

		<guid isPermaLink="false">http://www.pgblazer.com/?p=1258</guid>
		<description><![CDATA[It is an antihelminthic drug, a newer congener of mebendazole.  Mechanism of action is same as that of mebendazole. It inhibits glucose uptake into the helminth&#8217;s cells and depletes the glycogen storage. This is by binding to the beta-tubulin and preventing its polymerisation. Microtubules within the cells of the helminths disappear. The drugs inconsistently absorbed from the intestine. Absorption can increased by giving along with a fatty meal.
Adverse effects
Mostly GI symptoms, alopecia
Uses
Single dose 400 mg albenazole is given for hook worm, ascarias, enterobius. 400 mg daily for 3 days is ...   
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			<content:encoded><![CDATA[<p>It is an antihelminthic drug, a newer congener of mebendazole.  Mechanism of action is same as that of mebendazole. It inhibits glucose uptake into the helminth&#8217;s cells and depletes the glycogen storage. This is by binding to the beta-tubulin and preventing its polymerisation. Microtubules within the cells of the helminths disappear. The drugs inconsistently absorbed from the intestine. Absorption can increased by giving along with a fatty meal.</p>
<p><strong>Adverse effects</strong></p>
<p>Mostly GI symptoms, alopecia</p>
<p><strong>Uses</strong></p>
<p>Single dose 400 mg albenazole is given for hook worm, ascarias, enterobius. 400 mg daily for 3 days is given for strongyloides and tape worm. 400 mg twice daily for two weeks is given for neurocysticercosis. Should not be given in ocular cysticercosis as the reaction can cause blindness.</p>
<p>In hydatid disease, it is given as 400 mg twice daily for four weeks. Can be given before and after surgery and also in inoperable cases. Albenazole is also given in cutaneous larva migrans in a dose of 400 mg daily. Albendazole is used in filariasis along with diethyl carbamazine.</p>
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		<title>Metronidazole</title>
		<link>http://pgblazer.com/2009/06/metronidazole.html</link>
		<comments>http://pgblazer.com/2009/06/metronidazole.html#comments</comments>
		<pubDate>Wed, 10 Jun 2009 14:33:38 +0000</pubDate>
		<dc:creator>admin2</dc:creator>
				<category><![CDATA[Pharmacology]]></category>

		<guid isPermaLink="false">http://www.pgblazer.com/?p=1256</guid>
		<description><![CDATA[Metronidazole is a nitro-imidazole drug which has antiprotozoal and anti-anaerobe activity.
Spectrum
Protozoans - Entamoeba histolytic, Giardia lamblia, Trichomonas vaginalis
Bacteria &#8211; Camphylobacter jejuni, Helicobacter pylori, Fusobacterium, Bacteriodes fragilis, Spirochaetes, Clostridium perfringens, Clostridium difficile
Mechanism of action
Metronidazole has a nitro group which is converted into nitro radicle by the redox proteins of anaerobes. This acts as an electron acceptor and the availability of electrons to the electron transport chain is reduced. Certain organizms develop resistance to metronidazole by preventing the generation of nitro radicle.
Pharmacokinetics
Metronidazole is completely absorbed from the intestine and very little reaches the ...   
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			<content:encoded><![CDATA[<p>Metronidazole is a nitro-imidazole drug which has antiprotozoal and anti-anaerobe activity.</p>
<p><strong>Spectrum</strong></p>
<p>Protozoans - Entamoeba histolytic, Giardia lamblia, Trichomonas vaginalis</p>
<p>Bacteria &#8211; Camphylobacter jejuni, Helicobacter pylori, Fusobacterium, Bacteriodes fragilis, Spirochaetes, Clostridium perfringens, Clostridium difficile</p>
<p><strong>Mechanism of action</strong></p>
<p>Metronidazole has a nitro group which is converted into nitro radicle by the redox proteins of anaerobes. This acts as an electron acceptor and the availability of electrons to the electron transport chain is reduced. Certain organizms develop resistance to metronidazole by preventing the generation of nitro radicle.</p>
<p><strong>Pharmacokinetics</strong></p>
<p>Metronidazole is completely absorbed from the intestine and very little reaches the colon.</p>
<p><strong>Adverse effects</strong></p>
<p>CNS side effects, peripheral neuropathy, anorexia, nausea, metallic taste in mouth, head ache, neutropenia, rashes, thrombophlebitis when injected.</p>
<p><strong>Contra indications</strong></p>
<p>Chronic alcoholism because of disulfiram like reaction (Antabuse like reaction), neurological disorders, blood dyscrasias.</p>
<p><strong>Drug interactions</strong></p>
<p>Rifampicin and barbiturates induce hepatic metabolism. Cimetidine reduces the metabolism. Both these are by the action on CYP450.</p>
<p><strong>Uses of metronidazole</strong></p>
<p>Amoebiasis &#8211; 800 mg thrice daily for 7 to 10 days is given for amoebic liver abscess. In severe infections, intravenous therapy is initially given and followed by oral therapy. 400 mg thrice daily for mild intestinal amoebiasis.</p>
<p>It is also indicated in Giardiasis and Trichomoniasis.</p>
<p>Metronidazole is used in the triple drug regimen for Helicobacter pylori infection in peptic ulcer.</p>
<p>It can also be given in pseudomembranous colitis due to Clostridium difficile.</p>
<p>Metronidazole can be given for anaerobic infection after pelvic or colorectal surgery. Gentamicin is added as it is usually a mixed infection.</p>
<p>Trench mouth (ulcerative gingivitis) caused by fusobacterium is also treated with metronidazole.</p>
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		<title>Why is methylergometrine not used in the induction of labour?</title>
		<link>http://pgblazer.com/2009/06/why-is-methylergometrine-not-used-in-the-induction-of-labour.html</link>
		<comments>http://pgblazer.com/2009/06/why-is-methylergometrine-not-used-in-the-induction-of-labour.html#comments</comments>
		<pubDate>Wed, 10 Jun 2009 14:15:23 +0000</pubDate>
		<dc:creator>admin2</dc:creator>
				<category><![CDATA[Pharmacology]]></category>

		<guid isPermaLink="false">http://www.pgblazer.com/?p=1254</guid>
		<description><![CDATA[Methylergometrine produces non-physiological spasmodic contraction of the uterus in moderate to high doses and the uterus does&#8217;nt fully relax between the contractions. It also causes contraction of the lower segment of uterus. So the delivery of the fetus can be affected.
It is used after the delivery of the shoulder of the infant to reduce post partum hemorrhage. But it is indicated only in cases which have a higher risk of post partum hemorrhage.
   
 
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			<content:encoded><![CDATA[<p>Methylergometrine produces non-physiological spasmodic contraction of the uterus in moderate to high doses and the uterus does&#8217;nt fully relax between the contractions. It also causes contraction of the lower segment of uterus. So the delivery of the fetus can be affected.</p>
<p>It is used after the delivery of the shoulder of the infant to reduce post partum hemorrhage. But it is indicated only in cases which have a higher risk of post partum hemorrhage.</p>
<div class="plus-one-wrap"><g:plusone size="medium" href="http://pgblazer.com/2009/06/why-is-methylergometrine-not-used-in-the-induction-of-labour.html"></g:plusone></div>   
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		<title>Adverse effects of corticosteroids</title>
		<link>http://pgblazer.com/2009/06/adverse-effects-of-corticosteroids.html</link>
		<comments>http://pgblazer.com/2009/06/adverse-effects-of-corticosteroids.html#comments</comments>
		<pubDate>Wed, 10 Jun 2009 02:08:34 +0000</pubDate>
		<dc:creator>admin2</dc:creator>
				<category><![CDATA[Pharmacology]]></category>

		<guid isPermaLink="false">http://www.pgblazer.com/?p=1250</guid>
		<description><![CDATA[
Produces Cushing&#8217;s habitus &#8211; moon face, supraclavicular hump, trunkal obesity and relatively thin limbs, hirsuitim.
It causes proximal myopathy &#8211; shoulder, arms, hip, thigh
Fragility and thinning of skin &#8211; causes purple striae, especially on lower abdomen and thigh, easy bruisability and telangectasias
Decreased wound healing
Increased susceptibility to infections &#8211; flaring of tuberulosis can occur, predispose to oppurtunistic infections like candidiasis
Can cause posterior subcapsular cataract
Can cause peptic ulcer and silent perforation (two fold increase in risk)
Can cause hyperglycemia and may precipitate diabetes mellitus.
In pregnant females, steroids can cause gestational diabetes mellitus, hypertension and ...   
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			<content:encoded><![CDATA[<ol>
<li>Produces Cushing&#8217;s habitus &#8211; moon face, supraclavicular hump, trunkal obesity and relatively thin limbs, hirsuitim.</li>
<li>It causes proximal myopathy &#8211; shoulder, arms, hip, thigh</li>
<li>Fragility and thinning of skin &#8211; causes purple striae, especially on lower abdomen and thigh, easy bruisability and telangectasias</li>
<li>Decreased wound healing</li>
<li>Increased susceptibility to infections &#8211; flaring of tuberulosis can occur, predispose to oppurtunistic infections like candidiasis</li>
<li>Can cause posterior subcapsular cataract</li>
<li>Can cause peptic ulcer and silent perforation (two fold increase in risk)</li>
<li>Can cause hyperglycemia and may precipitate diabetes mellitus.</li>
<li>In pregnant females, steroids can cause gestational diabetes mellitus, hypertension and eclampsia</li>
<li>It may cause IUGR in the fetus</li>
<li>Hypertension due to salt water retention</li>
<li>Hypokalemia alkalosis</li>
<li>Edema</li>
<li>Osteoporosis &#8211; is an indication for withdrawl of steroids and can be prevented by concurrent administration of vitamin D, calcium bisphosphonates and estrogen in females and androgen in males.</li>
<li>Growth retardation in children</li>
<li>Suppression of hypothalamo-pituitary-adrenal axis</li>
<li>Steroid induced psychosis. Mild euphoria can occur more frequently.</li>
</ol>
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		<title>What is lactulose? Why is it preferred in patients with hepatic precoma?</title>
		<link>http://pgblazer.com/2009/06/what-is-lactulose-why-is-it-preferred-in-patients-with-hepatic-precoma.html</link>
		<comments>http://pgblazer.com/2009/06/what-is-lactulose-why-is-it-preferred-in-patients-with-hepatic-precoma.html#comments</comments>
		<pubDate>Wed, 10 Jun 2009 01:58:27 +0000</pubDate>
		<dc:creator>admin2</dc:creator>
				<category><![CDATA[Pharmacology]]></category>

		<guid isPermaLink="false">http://www.pgblazer.com/?p=1247</guid>
		<description><![CDATA[Lactulose is a semi-synthetic disaccharide composed of fructose and galactose. It is not absorbed in the intestine. It is broken down into osmotically more active products by the intestinal flora. This causes osmotic diarrhoea.
Hence it is used in the treatment of constipation. 10 gm twice daily is the dosage. It softens stools in one to three days.
Use in hepatic precoma
The products of lactulose degradation decreases the pH of the intestine. This converts the ammonia produced by the intestinal flora into NH4+ ions, thus decreasing the absorption. Hence it is used ...   
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			<content:encoded><![CDATA[<p>Lactulose is a semi-synthetic disaccharide composed of fructose and galactose. It is not absorbed in the intestine. It is broken down into osmotically more active products by the intestinal flora. This causes osmotic diarrhoea.</p>
<p>Hence it is used in the treatment of constipation. 10 gm twice daily is the dosage. It softens stools in one to three days.</p>
<p><strong>Use in hepatic precoma</strong></p>
<p>The products of lactulose degradation decreases the pH of the intestine. This converts the ammonia produced by the intestinal flora into NH4+ ions, thus decreasing the absorption. Hence it is used in the treatment of hepatic coma (porto-systemic encephalopathy). For this a higher dose of 20 gm three times daily or more may be needed.</p>
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