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How to Take Your Phosphate Binders
How to take your phosphate binders Information for renal patients Oxford Kidney Unit Page 2 What are phosphate binders? To reduce the amount of phosphate you absorb from your food you may have been prescribed a medicine called a phosphate binder. Phosphate binders work by binding (attaching) to some of the phosphate in food. This will reduce the amount of phosphate being absorbed into your blood stream. A list of phosphate binders and how to take them is shown below. Phosphate binder How to take it Calcichew (calcium carbonate) Chew thoroughly 10-15 minutes before or immediately before food Renacet (calcium acetate) Phosex (calcium acetate) Osvaren (calcium acetate and magnesium carbonate) Swallow whole after the first Renagel 2-3 mouthfuls of food (sevelemer hydrochloride) Renvela tablets (sevelemer carbonate) Alucaps (aluminium hydroxide) Renvela powder Dissolve in 60ml of water and (sevelemer carbonate) take after the first 2-3 mouthfuls of food Fosrenol tablets Chew thoroughly towards the (lanthanum carbonate) end/immediately after each meal Fosrenol powder Mix with a small amount of (lanthanum carbonate) food and eat immediately Velphoro Chew thoroughly after the first (sucroferric oxyhydroxide) 2-3 mouthfuls The phosphate binder you have been prescribed is: ……………………………………………………………………………………………………………………………………………………….. Page 3 How many phosphate binders should I take? You should follow the dose that has been prescribed for you. Your renal dietitian can advise how best to match your phosphate binders to your meal pattern, as well as which snacks require a phosphate binder. What happens if I forget to take my phosphate binder? For best results, phosphate binders should be taken as instructed. -
New Brunswick Drug Plans Formulary
New Brunswick Drug Plans Formulary August 2019 Administered by Medavie Blue Cross on Behalf of the Government of New Brunswick TABLE OF CONTENTS Page Introduction.............................................................................................................................................I New Brunswick Drug Plans....................................................................................................................II Exclusions............................................................................................................................................IV Legend..................................................................................................................................................V Anatomical Therapeutic Chemical (ATC) Classification of Drugs A Alimentary Tract and Metabolism 1 B Blood and Blood Forming Organs 23 C Cardiovascular System 31 D Dermatologicals 81 G Genito Urinary System and Sex Hormones 89 H Systemic Hormonal Preparations excluding Sex Hormones 100 J Antiinfectives for Systemic Use 107 L Antineoplastic and Immunomodulating Agents 129 M Musculo-Skeletal System 147 N Nervous System 156 P Antiparasitic Products, Insecticides and Repellants 223 R Respiratory System 225 S Sensory Organs 234 V Various 240 Appendices I-A Abbreviations of Dosage forms.....................................................................A - 1 I-B Abbreviations of Routes................................................................................A - 4 I-C Abbreviations of Units...................................................................................A -
Evaluation of Single Dose Sodium Polystyrene
Open Access Original Article Sodium Polystyrene Sulfonate For Management of Hyperkalemia Pak Armed Forces Med J 2019; 69 (1): 37-42 EVALUATION OF SINGLE DOSE SODIUM POLYSTYRENE SULFONATE FOR MANAGEMENT OF HYPERKALEMIA AND ITS EFFECT ON OTHER SERUM ELECTROLYTES Shoaib Alam, Azfar Athar Ishaqui, Masood Ahmed Khan, Adnan Iqbal, Syed Hameez Jawed, Farah Khalid, Mir Muhammad Uzairullah, Muhammad Talha*, Usman Ashfaq*, Najam Zehra* University of Karachi, Karachi Pakistan, *Hamdard University Karachi Pakistan ABSTRACT Objective: To assess the effectiveness of sodium polystyrene sulphonate in treating hyperkalemia and its effect on different serum electrolytes level. Study Design: Quasi-experimental study. Place and Duration of Study: Lyari general hospital, 500 bedded tertiary care public sector hospital at Karachi, from Jan 2017 to Mar 2017. Material and Methods: Hyperkalemic patients were included in study who fulfilled inclusion criteria and were administered with single STAT 30 grams dose of Sodium Polystyrene Sulfonate. Serum electrolytes such as sodium, chloride, magnesium, phosphate and calcium were measured before and after 2 hours of administration of Sodium Polystyrene Sulfonate. Paired t-test was used as tool for statistical analysis. Results: Significant (p<0.05) decrease in serum potassium level with mean decrease of 0.61 mmol/L was observed in hyperkalemic patients (n=83) after single dose of Sodium Polystyrene Sulfonate. Among 83 studied patient, 67 (81%) recovered from hyperkalemia. Besides, there was significant (p<0.05) increase in sodium level with a mean increase of 2.26 mmol/L. Serum magnesium and calcium levels were significantly decreased (p<0.05) with mean difference of 0.02mmol/L and 0.13mmol/L respectively. -
In-Class Targeted Therapies That Advance Patient Care
Passionately committed to improving the lives of patients by discovering, developing and commercializing first- in-class targeted therapies that advance patient care November 2020 Forward-Looking Statements To the extent that statements contained in this presentation are not descriptions of historical facts regarding Ardelyx, they are forward-looking statements reflecting the current beliefs and expectations of management made pursuant to the safe harbor of the Private Securities Reform Act of 1995, including statements regarding the potential for Ardelyx’s product candidates in treating the diseases and conditions for which they are being developed; Ardelyx’s expectation regarding the potential approval of its NDA for tenapanor for the control of serum phosphorus in chronic kidney disease (CKD) patients on dialysis and the expected timing thereof; the commercial potential for tenapanor for the control of serum phosphorus in CKD patients on dialysis, including Ardelyx’s expectation regarding the rate of adoption and use of tenapanor, if approved; Ardelyx’s expectations regarding the size of the patient population and the size of the market for tenapanor in CKD patients on dialysis, and the potential growth thereof; and Ardelyx’s expectations regarding the exhaustion of its current capital resources. Such forward-looking statements involve substantial risks and uncertainties that could cause the development of Ardelyx’s product candidates or Ardelyx's future results, performance or achievements to differ significantly from those expressed or implied by the forward-looking statements. Such risks and uncertainties include, among others, the uncertainties inherent in research and the clinical development process; the uncertainties associated with the regulatory approval process; and the uncertainties in the drug commercialization process. -
Phosphate Binders
Pharmacy Info Sheet Phosphate Binders calcium acetate, calcium carbonate (Tums, Calsan, Apocal, Ocal), calcium liquid, aluminum hydroxide (Basaljel, Amphojel), sevelamer (Renagel), lanthanum (Fosrenol) What it does: Phosphate binders are used to treat high Special considerations for lanthamum and blood phosphorus levels. sevelamer: Calcium acetate, calcium carbonate, calcium Lanthanum should be taken during or liquid, aluminum hydroxide, lanthanum and immediately after a meal. Taking a dose on an sevelamer bind dietary phosphate. When the empty stomach can cause nausea and kidneys fail, phosphorus builds up in the body vomiting. Chew the tablet completely before because the kidneys can no longer remove swallowing. DO NOT swallow tablets whole. much phosphorus. Phosphate binders are used to lower the amount of phosphorus Sevelamer should be taken just before eating. absorbed from food to limit development of Swallow the tablet whole – Renagel should not bone and blood vessel disease. be cut or chewed. The contents of sevelamer tablets expand in water and could cause Aluminum hydroxide and calcium carbonate choking if cut chewed or crushed. may also be prescribed as antacids. Calcium preparations may also be prescribed as Phosphate binders may interfere with the calcium supplements. Use them only as absorption of certain drugs such as iron prescribed. When these medications are supplements, antibiotics, digoxin, ranitidine, prescribed as calcium supplements or antiseizure, and antiarrhythmic medications. antacids, take between meals. If you are prescribed any of these drugs, take them at least 1 hour before or 3 hours after your How it works: phosphate binder. Kidney disease can cause phosphate to accumulate which results in bone and blood What to do if you miss a dose: vessel disease. -
SODIUM POLYSTYRENE SULFONATE, USP Cation-Exchange Resin
Kayexalate® SODIUM POLYSTYRENE SULFONATE, USP Cation-Exchange Resin DESCRIPTION Kayexalate, brand of sodium polystyrene sulfonate is a benzene, diethenyl-polymer, with ethenylbenzene, sulfonated, sodium salt and has the following structural formula: The drug is a cream to light brown finely ground, powdered form of sodium polystyrene sulfonate, a cation-exchange resin prepared in the sodium phase with an in vitro exchange capacity of approximately 3.1 mEq (in vivo approximately 1 mEq) of potassium per gram. The sodium content is approximately 100 mg (4.1 mEq) per gram of the drug. It can be administered orally or in an enema. CLINICAL PHARMACOLOGY As the resin passes along the intestine or is retained in the colon after administration by enema, the sodium ions are partially released and are replaced by potassium ions. For the most part, this action occurs in the large intestine, which excretes potassium ions to a greater degree than does the small intestine. The efficiency of this process is limited and unpredictably variable. It commonly approximates the order of 33 percent but the range is so large that definitive indices of electrolyte balance must be clearly monitored. Metabolic data are unavailable. INDICATION AND USAGE Kayexalate is indicated for the treatment of hyperkalemia. CONTRAINDICATIONS Kayexalate is contraindicated in the following conditions: patients with hypokalemia, patients with a history of hypersensitivity to polystyrene sulfonate resins, obstructive bowel disease, neonates with reduced gut motility (postoperatively or drug induced) and oral administration in neonates (see PRECAUTIONS). WARNINGS Intestinal Necrosis: Cases of intestinal necrosis, which may be fatal, and other serious gastrointestinal adverse events (bleeding, ischemic colitis, perforation) have been reported in association with Kayexalate use. -
Dorset Medicines Advisory Group
Dorset Medicines Advisory Group SHARED CARE GUIDELINE FOR THE USE OF PHOSPHATE BINDERS IN THE MANAGEMENT OF HYPERPHOSPHATAEMIA IN PATIENTS WITH CHRONIC KIDNEY DISEASE. INDICATION This document provides guidance for the prescribing of phosphate binders for the management of hyperphosphatemia in patients receiving haemodialysis or peritoneal dialysis and patients with chronic kidney disease stage 4 or 5 who are not receiving dialysis. This shared care guideline covers adult patients under the care of the Dorset Renal Unit. Patients with chronic renal failure have reduced ability to excrete phosphate. Phosphate accumulation enhances parathyroid activity and leads to the calcification of arteries, significantly contributing to the excess cardiovascular morbidity in these patients, especially in younger age groups. Adequate control of serum phosphate levels is thought to be beneficial for the prevention of vascular and cardiac calcification in patients with renal failure and control of parathyroid hormone. A number of oral phosphate binders are available which may be used in the context of a multiple therapeutic approach. These include calcium acetate, calcium carbonate, calcium acetate/magnesium carbonate, lanthanum, sevelamer and sucroferric oxyhydroxide. These products may be used in combination with 1-hydroxycholecalciferol (alfacalcidol) or one of its analogues and/or cinacalcet to control the development of secondary hyperparathyroidism and renal bone disease. A calcium-based phosphate binder is generally used as the initial phosphate binder therapy for the treatment for hyperphosphatemia. Calcium acetate is preferred over calcium carbonate due to its lower elemental calcium content for the equivalent phosphate binding capacity, however patient preference in formulation should be taken into consideration. A non-calcium-based phosphate binder should be used in patients who cannot tolerate a calcium-based phosphate binder, whose serum calcium exceeds 2.5mmol/L or whose parathyroid levels are less than 15pmol/L. -
AMBERLITE™ IRP69 Ion Exchange Resin Pharmaceutical Grade Cation Exchange Resin (Sodium Polystyrene Sulfonate USP)
Product Data Sheet AMBERLITE™ IRP69 Ion Exchange Resin Pharmaceutical Grade Cation Exchange Resin (Sodium Polystyrene Sulfonate USP) Description AMBERLITE™ IRP69[1] resin is an insoluble, strongly acidic, sodium form cation exchange resin supplied as a dry, fine powder. AMBERLITE™ IRP69 Resin is suitable for use in pharmaceutical applications, both as an active ingredient and as a carrier for basic (cationic) drugs. It can be used for sustained release applications with compatible coating technologies. [1] The use of AMBERLITE™ pharmaceutical grade ion exchange resins as components of drug formulations is subject to the Food, Drug, and Cosmetic Act as amended. Regulatory Status A Drug Master File for AMBERLITE™ IRP69 is maintained with the United States Food and Drug Administration. Letters of authorization granting access to the file by FDA in support of NDA and ANDA submittals will be provided upon request. Similar help can also be offered in support of the registration of formulations containing AMBERLITE™ IRP69 in many other countries world- wide. AMBERLITE™ IRP69 is manufactured in accordance with Good Manufacturing Practices (cGMP) for bulk pharmaceutical chemicals Typical Properties AMBERLITE™ IRP69 complies with the compendial specifications for Sodium Polystyrene Sulfonate USP when tested in conformance to the compendial test methods presented in current USP/NF. Physical Properties Copolymer Styrene-divinylbenzene Type Strong acid cation Functional Group Sulfonic acid Physical Form Fine powder Chemical Properties Ionic Form as Shipped Na+ Heavy metals content [1] ≤ 10 ppm Potassium exchange capacity [1] 110–135 mg/g Water content [1] 10.0% maximum Ammonia salts [1] Negative to litmus paper Sodium content [1] 9.4%–11.5% Styrene content [1] 1 ppm maximum Particle Size § > 0.150 mm 1.0% maximum > 0.075 mm 10.0–25.0% §[1] Appears in current USP/NF Page 1 of 6 Form No. -
The Indirect Implication of SARS-Cov-2 Resulting in Kayexalate Toxicity in a Patient with Acute Kidney Injury
CODON P U B L I C A T I O N S Journal of Renal and Hepatic Disorders CASE REPORT: NEPHROLOGY The Indirect Implication of SARS-CoV-2 Resulting in Kayexalate Toxicity in a Patient with Acute Kidney Injury Charles E Middleton, IV, MD, William Daley, MD, Neha Varshney, MD Department of Pathology, University of Mississippi Medical Center, Jackson, MS, USA Abstract The clinical features of corona virus disease 2019 (COVID-19) are variable, but the majority of patients experience mild flu-like symptoms. The cases of severe disease include complications such as progressive pneumonia, acute kidney injury (AKI), multi-organ failure, and even death. This paper explores the association between COVID-19 and its effect on multiple organ systems and how the subsequent treatment of this dis- ease can itself lead to morbidity and mortality. We present a case that emphasizes the life-threatening gastrointestinal complications associated with the treatment of AKI in a patient with COVID-19. We conclude that the patients whose treatment regimens utilize medical resins should be closely monitored for gastrointestinal complications so as to mitigate the known adverse effects associated with these drugs, such as colonic mucosal ulceration, perforation, or even death. Keywords: acute kidney injury; colonic perforation; COVID-19; Kayexalate; resins; sevelamer Received: 25 November 2020; Accepted after revision: 5 February 2021; Published: 27 February 2021. Author for correspondence: Neha Varshney, MD, Assistant Professor, Department of Pathology, University of Mississippi Medical Center, 2500 North State Street, Jackson, MS 39216-4500, USA. Email: [email protected] How to cite: Middleton CE, et al. -
Estonian Statistics on Medicines 2016 1/41
Estonian Statistics on Medicines 2016 ATC code ATC group / Active substance (rout of admin.) Quantity sold Unit DDD Unit DDD/1000/ day A ALIMENTARY TRACT AND METABOLISM 167,8985 A01 STOMATOLOGICAL PREPARATIONS 0,0738 A01A STOMATOLOGICAL PREPARATIONS 0,0738 A01AB Antiinfectives and antiseptics for local oral treatment 0,0738 A01AB09 Miconazole (O) 7088 g 0,2 g 0,0738 A01AB12 Hexetidine (O) 1951200 ml A01AB81 Neomycin+ Benzocaine (dental) 30200 pieces A01AB82 Demeclocycline+ Triamcinolone (dental) 680 g A01AC Corticosteroids for local oral treatment A01AC81 Dexamethasone+ Thymol (dental) 3094 ml A01AD Other agents for local oral treatment A01AD80 Lidocaine+ Cetylpyridinium chloride (gingival) 227150 g A01AD81 Lidocaine+ Cetrimide (O) 30900 g A01AD82 Choline salicylate (O) 864720 pieces A01AD83 Lidocaine+ Chamomille extract (O) 370080 g A01AD90 Lidocaine+ Paraformaldehyde (dental) 405 g A02 DRUGS FOR ACID RELATED DISORDERS 47,1312 A02A ANTACIDS 1,0133 Combinations and complexes of aluminium, calcium and A02AD 1,0133 magnesium compounds A02AD81 Aluminium hydroxide+ Magnesium hydroxide (O) 811120 pieces 10 pieces 0,1689 A02AD81 Aluminium hydroxide+ Magnesium hydroxide (O) 3101974 ml 50 ml 0,1292 A02AD83 Calcium carbonate+ Magnesium carbonate (O) 3434232 pieces 10 pieces 0,7152 DRUGS FOR PEPTIC ULCER AND GASTRO- A02B 46,1179 OESOPHAGEAL REFLUX DISEASE (GORD) A02BA H2-receptor antagonists 2,3855 A02BA02 Ranitidine (O) 340327,5 g 0,3 g 2,3624 A02BA02 Ranitidine (P) 3318,25 g 0,3 g 0,0230 A02BC Proton pump inhibitors 43,7324 A02BC01 Omeprazole -
Nephrology II BONE METABOLISM and DISEASE in CHRONIC KIDNEY DISEASE
Nephrology II BONE METABOLISM AND DISEASE IN CHRONIC KIDNEY DISEASE Sarah R. Tomasello, Pharm.D., BCPS Reviewed by Joanna Q. Hudson, Pharm.D., BCPS; and Lisa C. Hutchison, Pharm.D., MPH, BCPS aluminum toxicity. Adynamic bone disease is referred to as Learning Objectives low turnover disease with normal mineralization. This disorder may be caused by excessive suppression of PTH 1. Analyze the alterations in phosphorus, calcium, vitamin through the use of vitamin D agents, calcimimetics, or D, and parathyroid hormone regulation that occur in phosphate binders. In addition to bone effects, alterations in patients with chronic kidney disease (CKD). calcium, phosphorus, vitamin D and PTH cause other 2. Classify the type of bone disease that occurs in patients deleterious consequences in patients with CKD. Of these, with CKD based on the evaluation of biochemical extra-skeletal calcification and increased left ventricular markers. mass have been documented and directly correlated to an 3. Construct a therapeutic plan individualized for the stage increase in cardiovascular morbidity and mortality. The goal of CKD to monitor bone metabolism and the effects of of treatment in patients with CKD and abnormalities of bone treatment. metabolism is to normalize mineral metabolism, prevent 4. Assess the role of various treatment options such as bone disease, and prevent extraskeletal manifestations of the phosphorus restriction, phosphate binders, calcium altered biochemical processes. supplements, vitamin D agents, and calcimimetics In 2003, a non-profit international organization, Kidney based on the pathophysiology of the disease state. Disease: Improving Global Outcomes, was created. Their 5. Devise a therapeutic plan for a specific patient with mission is to improve care and outcomes for patients with alterations of phosphorus, calcium, vitamin D, and CKD worldwide by promoting, coordinating, collaborating, intact parathyroid hormone concentrations. -
Case Report Sevelamer Carbonate Crystal-Induced Colitis
Hindawi Case Reports in Gastrointestinal Medicine Volume 2020, Article ID 4646732, 4 pages https://doi.org/10.1155/2020/4646732 Case Report Sevelamer Carbonate Crystal-Induced Colitis T. Lai ,1 A. Frugoli ,2 B. Barrows,3 and M. Salehpour4 1Community Memorial Health System, Graduate Medical Education, Ventura, CA, USA 2Community Memorial Health System, Graduate Medical Education, Department of Internal Medicine, Pacific Inpatient Physicians, Ventura, CA, USA 3Community Memorial Hospital, Department of Pathology, Ventura, CA, USA 4Community Memorial Hospital, Department of General Surgery, Ventura, CA, USA Correspondence should be addressed to T. Lai; [email protected] Received 19 February 2020; Accepted 30 March 2020; Published 24 July 2020 Academic Editor: Olga I. Giouleme Copyright © 2020 T. Lai et al. )is is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Hyperphosphatemia is a common and well-described complication of end-stage renal disease. Despite strict dietary constraints and compliance, phosphate binders such as calcium acetate and/or sevelamer carbonate are also needed to treat secondary hyperparathyroidism. )is case vignette describes an underrecognized adverse effect of a phosphate binder, sevelamer carbonate, inducing colitis in a 47-year-old male with insulin-dependent diabetes complicated by end-stage renal disease. He presented for recurrent abdominal pain with associated nausea and was found to have multiple circumferential lesions on computed to- mography including distal ascending, transverse, and proximal descending colon. Colonoscopy demonstrated nearly obstructing lesions worrisome for colonic ischemia or inflammatory bowel disease. Pathological review of histology demonstrated ragged colonic mucosa with ulcerative debris and nonpolarizing crystalline material at the sites of ulceration, morphologically consistent with the phosphate binder, sevelamer carbonate.