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Carbonic Anhydrase Inhibitors and Activators: Small
Carbonic Anhydrase Inhibitors and Activators: Small

... Cytosol Cytosol Membrane-bound Cytosol Cytosol Membrane-bound Unknown Membrane-bound ...
Management and Prevention of Upper GI Bleeding
Management and Prevention of Upper GI Bleeding

... acute bleeding ulcers. A possible mechanism involved in increased false-negative rates of H. pylori testing is the pH buffering effect of blood; higher alkalinity has been associated with higher rates of false-negative results. Nonsteroidal anti-inflammatory drugs, including aspirin, continue to b ...
Abstract
Abstract

... If total drug concentrations are increased beyond the point at which the binding sites on albumin are saturated, biologically active free-drug concentrations increase disproportionately to the increasing total drug concentration. The clearance of NSAIDs is usually by hepatic metabolism, with product ...
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... Use in Ambulatory Patients ULTRAM® may impair the mental and or physical abilities required for the performance of potentially hazardous tasks such as driving a car or operating machinery. The patient using this drug should be cautioned accordingly. Use With MAO Inhibitors and Serotonin Re-uptake In ...
Curr.Med. Chem._Martínez, A._2015 - digital
Curr.Med. Chem._Martínez, A._2015 - digital

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Drugs acting on RAAS by Dr Vignesh S
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Basics Pharmacology Review - Dr. Roland Halil

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View Prescribing Details

... Carefully consider the potential benefits and risks of Ranoxen™ Plus (Naproxen and Esomeprazole) and other treatment options before deciding to use Ranoxen™ Plus (Naproxen and Esomeprazole). Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals. I ...
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Acetaminophen and Salicylates Toxicity and Management

... • Temple AR. Acute and chronic effects of aspirin toxicity and their treatment. Arch Intern Med 1981;141:367 ...
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Discovery and development of direct thrombin inhibitors



Direct thrombin inhibitors (DTIs) are a class of anticoagulant drugs that can be used to prevent and treat embolisms and blood clots caused by various diseases. They inhibit thrombin, a serine protease which affects the coagulation cascade in many ways. DTIs have undergone rapid development since the 90's. With technological advances in genetic engineering the production of recombinant hirudin was made possible which opened the door to this new group of drugs. Before the use of DTIs the therapy and prophylaxis for anticoagulation had stayed the same for over 50 years with the use of heparin derivatives and warfarin which have some well known disadvantages. DTIs are still under development, but the research focus has shifted towards factor Xa inhibitors, or even dual thrombin and fXa inhibitors that have a broader mechanism of action by both inhibiting factor IIa (thrombin) and Xa. A recent review of patents and literature on thrombin inhibitors has demonstrated that the development of allosteric and multi-mechanism inhibitors might lead the way to a more safer anticoagulant.
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