Piperazine (generic‚ Vermizine) Oral: piperazine citrate tablets equivalent to 250 mg of the hexahydrate; piperazine citrate syrup equivalent to 500 mg of the hexahydrate per 5 mL Praziquantel (Biltricide; others outside the USA) Oral: 600 mg tablets (other strengths outside the USA) Pyrantel pamoate (Antiminth‚ Combantrin‚ Pin-rid‚ Pin-X) Oral: 50 mg (base)/mL suspension; 62.5 mg (base) capsules (available without prescription in the USA) Suramin (Bayer 205‚ others) Parenteral: ampules containing
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Technol.‚ 100: 6137-6140. Megateli‚ S.‚ Semsari‚ S.‚ Couderchet‚ M.‚ (2009). Toxicity and removal of heavy metals (cadmium‚ copper and zinc) by Lemna gibba. Ecotoxicol. Environ. Saf. 72:1774-1780. Miretzky‚ P.‚ Saralegui‚ A.‚ Cirelli‚ A.F.‚ (2004). Aquatic macrophytes potential for the simultaneous removal of heavy metals (Buenos Aires‚ Argentina). Chemosphere‚ 57: 997-1005. Movahedian‚ H.‚ Bina‚ B.‚ Asghari‚ G.H.‚ (2005). Toxicity Evaluation of Wastewater Treatment Plant Effluents Using Daphnia magna
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Select lead agonist. Renal CP toxicity reduction will be a major driver for lead selection (50% or greater protective effects on CP renal toxicity using serum creatinine‚ inulin based GFR‚ and CP-AKI injury score) selecting a peptide if it is equal or better than rRNLS. Milestone (M1): Use the improved models including ours‚ to compare
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aldehydes (R-CHO) (e.g. acetaldehyde) or to carboxylic acids (R-CO2H)‚ while the oxidation of secondary alcohols (R1R2CH-OH) normally terminates at the ketone (R1R2C=O) stage. Tertiary alcohols (R1R2R3C-OH) are resistant to oxidation. Ethanol’s toxicity is largely caused by its primary metabolite‚ acetaldehyde (systematically ethanal)[2][3] and secondary metabolite‚ acetic acid.[3][4][5][6] All primary alcohols are broken down into
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Final Exam Part 2 1. Antiarrhythmic drugs primarily affect the activity of the following ion channels except A. Cl B. Na C. K D. Ca 2. What is a life-threatening arrhythmia caused by electrical conduction disturbances? A. Atrial fibrillation B. Ventricular fibrillation C. Ectopic foci D. Premature ventricular contraction 3. A common adverse effect from quinidine overdosage is A. Hypertension B. Tachypnea C. Cinchonism D. Dry mouth 4. Disopyramide produces a _____ in conduction
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1.0 INTRODUCTORY STATEMENT AND GENERAL INVESTIGATIONAL PLAN 1.1. Drug and Broad Objectives Harvoni is a fixed-dose combination of ledipasvir and sofosbuvir for the treatment for the chronic hepatitis C. Ledipasvir is an inhibitor of the HCV NS5A protein‚ which is required for viral replication. Resistance selection in cell culture and cross-resistance studies indicate ledipasvir targets NS5A as its mode of action. Sofosbuvir is an inhibitor of the HCV NS5B RNA-dependent RNA polymerase‚ which is
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Prevention Of Atheromatous Heart Disease By O.P. Agarwal‚ M.D.‚ F.I.C.A. Angiology‚ Vol 36‚ Number 8‚ August 1985 Presented at the 31st Annual Meeting‚ American College of Angiology and 26th Annual Meeting‚International College of Angiology‚ November 5‚ 1984. Abstract Five thousand patients of atheromatous heart disease‚ presented as angina pectoris‚ were studied over a period of five years. After adding the “Husk of Isabgol” and “Aloe vera” (an indigenous plant known as ghee-guar-ka-paththa)
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Chapter 14: Critical Care Nursing (Pg 338-366‚ 412-437) Chapter 15: Cardiovascular Disorders Coronary Artery Disease Description and Etiology The biggest contributor to cardiovascular system- related morbidity and mortality is coronary artery disease. Atherosclerosis is a progressive disease that affects arteries throughout the body. (CAD) Risk Factors for CAD 1. Age‚ Gender‚ Race (non-modifiable) a. More common in men than women b. Higher in women over 75 years of age 2. Family History
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SINGAPORE 117528 SINGAPORE Telephone Fax : : +65 6779 1200 +65 6779 1822 Emergency telephone number Emergency Phone # : 1-800-262-8200 2. HAZARDS IDENTIFICATION 2.1 GHS Classification Acute toxicity‚ Oral (Category 4) Skin irritation (Category 2) Eye irritation (Category 2) Specific target organ toxicity - single exposure (Category 3)‚ Respiratory system 2.2 GHS Label elements‚ including precautionary statements Pictogram Signal word Warning Hazard statement(s) H302 H315 H319 H335 Harmful
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colorectal cancer (n ¼ 23 patients)‚ lung cancer (n ¼ 6 patients)‚ gastroesophageal cancer (n ¼ 6 patients)‚ and pancreatic cancer (n ¼ 3 patients)‚ received _1 dose of study drug. Nausea‚ vomiting‚ and diarrhea were the principal dose-limiting toxicities and led to the maximum tolerated doses of 1.3 mg/m2 bortezomib and 125 mg/m2 irinotecan. The most common grade _3 bortezomib-related nonhematologic adverse events were fatigue (n ¼ 5 episodes)‚ diarrhea (n ¼ 4 episodes)‚ and nausea (n ¼ 4 episodes)
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