Effect of Magnesium Sulfate (A Laxative) on Accommodation and Converegence Function by Osude-Uzodike, E

Total Page:16

File Type:pdf, Size:1020Kb

Effect of Magnesium Sulfate (A Laxative) on Accommodation and Converegence Function by Osude-Uzodike, E EFFECT OF MAGNESIUM SULFATE (A LAXATIVE) ON ACCOMMODATION AND CONVEREGENCE FUNCTION BY OSUDE-UZODIKE, E. B. AND AKANOH, R. N. DEPARTMENT OF OPTOMETRY,ABIA STATE UNIVERSITY UTURU, ABIA STATE, NIGERIA Email:[email protected] *Corresponding author ABSTRACT Magnesium sulfate (MgSO4 ), a laxative and over-the-counter drug is abusively used by individuals to relieve constipation, hard and inconsistent stool, and after effect of poor diet. Thirty young volunteers of both sexes were administered 15g of MgSO4 effervescence laxative. The effect of the drug on accommodation, accommodative convergence /accommodation (AC/A) ratio, near point of convergence (NPC) and lateral phoria at far and near were studied by measuring these visual functions pre and post MgSO4 administration. Results showed that there was no effect on accommodation, NPC decreased with a peak percentage decrease of 27.5%, lateral phoria at far had peak percentage decrease of 375.4%, lateral phoria at near had peak percentage decrease of 50.9% and AC/A ratio a percentage decrease of 43.4%. These effects were found to be significant (P<0.05). Eye care practitioners should advise their patients to desist from abusing laxatives and other over-the-counter drugs and should consider its effects during analysis of visual test finding for effective patient care. KEYWORDS: Magnesium sulfate, Laxatives,Accommodation, Convergence, Near point of convergence, Lateral phoria. INTRODUCTION rectal reflex and laxatives dependent constipation3 . Laxatives of various types are widely prescribed Chronic use of laxatives can become habituating and more widely purchased without prescription leading to the development of a dilated atonic indicating a cultural pre-occupation with laxative colon, which requires increasing laxative 1 “regularity” of intestinal walls and stool . They are use with little success5,6 . generally described as over-the-counter (OTC) Magnesium sulfate also known as Epsom salt products2 . or bitter salt9 is a hydrate salt with a chemical name Laxative drugs that affect the fecal constituent of magnesium sulfate heptahydrate9,10 . Chemical accelerate elimination of stool from the rectum3 . 11 formula is MgSO4 . 7H 2 O and trade name is They can be used to relieve constipation during Andrews liver salt. pregnancy, in those whose bowel motility has been Dried magnesium sulfate is an osmotic laxative4,11 altered through use of anticholinergic drugs, or a saline laxative12,13 that acts by increasing the narcotics, antihelmintic therapy and generally bulk of the stools through attracting and holding 4 short-term treatment of constipation and other large amounts of fluids, the increased bulk results possible conditions that can lead to constipation inthe mechanical stimulationof peristalsis4 . like condition within the colon and rectum or Systemically administered drugs are known to 5,6,7 externally . The external conditions can be as a produce effect in the eye when sufficient result of poor dietary habits (most common), concentration of the drug reaches its site of action medications and psychological factors. Bowel- in the eye and can influence various clinical conscious individuals easily abuse laxatives. procedures and visual test results. Laxatives like other being an OTC drugs, the result The adverse effect of MgSO4 in the body may be similar to simple, prolonged diarrhea with system can also affect the eyes hence it is worth- symptoms of potassium ion (K+) depletion, while that the ocular and visual effects (if any) are intestinal hypotonus, alkalosis and muscle known by the primary eye-care practitioners for 8 weakness . The use of laxatives may become better patient management. habitual and can lead to hyponatremia, loss of the JNOA - VOL 10, 2003 8 MATERIALSANDMETHOD 72hours post ingestion (see fig. 2). Zcal (8.819) was Effect of magnesium sulfate on found to be greater than Ztab (1.96 0.05 ), hence, it was accommodation and convergence functions is a concluded that ingestion of 15g of MgSO4 had prospective and clinically based study. Abia State significant effect on NPC. The minus signs showed University Optometry Clinics (Uturu and that the values were less than the baseline value. Umuahia) were used for the study. Thirty healthy Analysis of data obtained showed that lateral volunteers between the ages of 18 and 34years phoria at far decreased gradually from 2hrs after were used. Those volunteers with ocular MgSO4 intake by -0.82±0.16Δ D and had a peak pathology, refractive error and history of systemic decrease 4hrs after intake with induced change of - abnormalities were screened out as suchconditions 2.29±0.28Δ D.The peak percentage induced might jeopardize the test results. Experimental change was 375. 4%. It then returned to baseline subjects were well fed during the period of the value 72hrs post ingestion. Fig. 3 showed the study and they served as their own control. graphical representation of this effect. Statistical The visual functions of i nt e res t : analysis showed a significant effect of MgSO4 on accommodation (using minus-lens-to-blur lateral phoria at far (Z 10.6> Z 1.96 at 96% method), lateral phoria (using Von-Graefe cal tab confidence interval). technique), NPC (using PD rule) and AC/A ratio Fig. 4 represents the analysis of the MgSO (using the induced phoria method) were measured 4 pre and post MgSO administration. The research effect on lateral phoria at near. Lateral phoria at 4 near decreased gradually from 2hrs after MgSO lasted fora period of 3days. Pilot studyshowedthat 4 systemic effects start 2hours after 15g MgSO intake by 0.98±0.18Δ D. Peak induced change was 4 obtained 4hrs after intake with induced change of - ingestion, hence, measurement of visual functions 2.8±0.31Δ D and percentage induced change of started 2hours post administration of 15g MgSO 4 50.9%. It returned to baseline value 72hrs post on volunteer subjects. The visual functions were ingestion. Statistically, the effect was shown to be reassessed at intervals of 30minuts till 2hours after significant (Z 7.68>Z 1.96). MgSO ingestion and then once daily for the next cal tab 4 From fig. 5, AC/A ratio decreased gradually 3days. Data obtained were analyzed using tables, from 2hrs after MgSO by 0.56±0.14. Peak figures andZ-test forsignificance ofthe result. 4 intake decrease was obtained 4hrs after intake with Magnesium sulfate used was manufactured induced change of -1.98±0.26 and percentage from Glaxo Smith Kline (Nig. PLC) with batch no. induced change of 43.4%. AC/A gradually 034E. increased and returned to baseline value 72hrs post ingestion. Statistically, the induced effect was RESULTS foundto be significant (Z 5.89>Z 1.96). The test substance, Magnesium sulfate cal tab heptahydrate was administered on volunteer subjects and its effect on visual functions of DISCUSSION interest was measured. The analysis of the data Analysis of data obtained as a result of administration of 15g MgSO , a laxative, on obtained is presented below. The symbol used in 4 the graphs: Y1, Y2, Y3, Y4, Y5, Y6, Y7, Y8, volunteer subjects showed no effect on amplitude represents 2hours, 2½hrs, 3hrs, 3½hrs, 4hrs, of accommodation (P>0.05) but significant effect 4½hrs, 24hrs, 48hrs, and 72hrs post ingestion of on NPC, lateral phoria at far and near and AC/A magnesium sulfate respectively. ratio(see figs.2-5; P<0.05). These effects can be explained on the stimulation Fig. 1 showed that MgSO4 has no effect on Amplitude of Accommodation (A.A). When the of parasympathetic nervous system in stimulating data obtained was subjected to statistical analysis, peristalsis, as the bulk of the stool is increased4,7,12,14,15 . Postganglionic parasympathetic Ztab (1.96 0.05 ) was found to be greater than Z cal (0.32) confirming the graphical representation. fibres stimulate accommodation while NPC deceased gradually from 2hours after preganglionic parasympathetic fibres stimulate convergence. In both the preganglionic and magnesium sulfate intake by 1.32cm, peak postganglionic parasympathetic fibre stimulation, decrease was obtained 4hrs after intake with 16,17 induced change of -2.8cm and percentage induced acetylcholine will be released . Ingestion of MgSO stimulates peristalsis and change of27.59%. It started to increase from 24 hrs 4 post ingestion and returned to baseline value suppresses myenteric plexus, which is also innervated by the preganglionic parasympathetic 9 JNOA - VOL 10, 2003 system. The information is sent to the brain stem synkinesis between accommodation and where the neurons of the reticular activating convergence and the accommodation by MgSO4 system processes the information and in turn administration can be explained by the fact that stimulates the motor part of the vagus nerve and ciliary body and iris sphincter muscles involved in motor part of any other cranial nerve (oculomotor accommodative action are supplied by autonomic nerve inclusive). Innervations of the motor part of fibres of oculomotor nerve not the motor fibres of the oculomotor nerve led to stimulation of medial oculomotor nerve which is being affected by recti muscles of both eyes increasing the tonic MgSO4 . convergence which results in decreased values of In conclusion, MgSO4 effervescence, a NPC and lateral phoria (far and near) tending laxative and OTC drugs, when abused can lead to towardsesophoria (as shown infigs 2-5). over convergence and esophoric conditions which The effect of 15g MgSO4 on AC/A ratio is a could degenerate to binocularity problem. Primary cumulative effect and is supported by Borish's18 eye care practitioners should take note of the use of assertion that central nervous depressants decrease over-the-counter drugs and advice patients against AC/A ratio by selectively reducing convergence its abuse. They should also consider it while response without affecting accommodation and prescribing to the patients as it affects some visual that generally, the action of drugs indicate a test results.
Recommended publications
  • Magnesium Sulfate for Neuroprotection Practice Guideline
    [Type text] [Type text] Updated June 2013 Magnesium Sulfate for Neuroprotection Practice Guideline I. Background: Magnesium sulfate has been suggested to have neuro-protective effect in retrospective studies from 1987 and 1996. Since that time three randomized control trials have been performed to assess magnesium therapy for fetal neuroprotection. These studies have failed to demonstrate statistically significant decrease in combined outcome of cerebral palsy and death or improved overall neonatal survival. However, these results did demonstrate a significant decrease in cerebral palsy of any severity by 30%, particularly moderate-severe cerebral palsy (40-45%). The number needed to treat at less than 32 weeks gestation is 56. The presumptive mechanism of action for magnesium sulfate focuses on the N-methyl-D-aspartate receptor. Additional magnesium effects include calcium channel blockade resulting in cerebrovascular relaxation and magnesium mediated decreases in free radical production and reductions in the production of inflammatory cytokines. Magnesium sulfate should not be used as a tocolytic simply because of the potential for neuro-protective effects. In a recent committee opinion, ACOG states “the available evidence suggests that magnesium sulfate given before anticipated early preterm birth reduces the risk of cerebral palsy in surviving infants” but specific guidelines should be established. “The U.S. FDA has recently changed the classification of magnesium sulfate injection from Category A to Category D. However, this change was based on a small number of neonatal outcomes in cases in which the average duration of exposure was 9.6 weeks. The ACOG Committee on Obstetric Practice and the Society for Maternal-Fetal Medicine continue to support the use of magnesium sulfate in obstetric care for appropriate conditions and for appropriate, short term (usually less than 48 hours) durations of treatment.” II.
    [Show full text]
  • Calcium Gluconate
    CALCIUM GLUCONATE CLASSIFICATION Minerals and electrolytes TRADE NAME(S) Calcium Gluconate 10% (for IV use) Calcium Gluconate gel 2.5% (for topical use) DESIRED EFFECTS Lower potassium levels; pain relief and neutralizing fluoride ion MECHANISM OF ACTION Calcium is the primary component of skeletal tissue. Bone serves as a calcium depot and as a reservoir for electrolytes and buffers. INDICATIONS Suspected hyperkalemia in adult PEA/Asystole Antidote for calcium channel blocker overdose and magnesium sulfate toxicity Gel is used for hydrofluoric acid burns Suspected hyperkalemia with adult crush injury or peaked T-waves on EKG CONTRAINDICATIONS Should not be given to patients with digitalis toxicity Should be used with caution in patients with dehydration ADVERSE REACTIONS When given too rapidly or to someone on digitalis, can cause sudden death from ventricular fibrillation May cause mild to severe IV site irritation SPECIAL CONSIDERATIONS Must either use a different IV line or flush line with copious normal saline if being given with sodium bicarbonate. When used on hydroflouric acid burns, relief of pain is the only indication of treatment efficacy. Therefore, use of analgesic agents is not recommended. DOSING REGIMEN Suspected hyperkalemia in adult PEA/asystole or adult crush injury, or evidence of EKG changes (Ex. peaked T-waves) o Calcium gluconate 10% 15-30 ml IV/IO over 2-5 minutes KNOWN calcium channel blocker overdose - administer 3 grams IV/IO may repeat dose in 10 minutes if no effect. Hydrofluoric acid burns apply calcium gluconate gel 2.5% every 15 minutes to burned area and massage continuously until pain disappears.
    [Show full text]
  • 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
    [Show full text]
  • Magnesium Sulfate
    MODULE III MAGNESIUM SULFATE Manual for Procurement & Supply of Quality-Assured MNCH Commodities MAGNESIUM SULFATE INJECTION, 500 MG/ML IN 2-ML AND 10-ML AMPOULE GENERAL PRODUCT INFORMATION Pre-eclampsia and eclampsia is the second-leading cause of maternal death in low- and middle-income countries. It is most often detected through the elevation of blood pressure during pregnancy, which can be followed by seizures, kidney and liver damage, and maternal and fetal death, if untreated. Magnesium sulfate is recognized by WHO as the safest, most effective, and lowest-cost medicine for treating pre-eclampsia and eclampsia. It is also considered an essential medicine by the UN Commission on Life-Saving Commodities for Women and Children. Other anticonvulsant medicines, such as diazepam and phenytoin, are less effective and riskier. Magnesium sulfate should be the sole first-line treatment of pre-eclampsia and eclampsia that should be procured over other anticonvulsants and made available in all health facilities to help lower maternal death rates and improve overall maternal health. MSꟷ1 | Manual for Procurement & Supply of Quality-Assured MNCH Commodities Magnesium Sulfate KEY CONSIDERATIONS IN PROCUREMENT Procurement should be made from trusted sources. This includes manufacturers prequalified by WHO or approved by a SRA for magnesium sulfate injection and 1. those with a proven record of quality products. Procurers need to focus on product quality to ensure that it is sterile and safe for patient use as magnesium sulfate is an injectable medicine. 2. KEY QUALITY CONSIDERATIONS Product specification Products that are procured must comply with pharmacopoeial specifications, such as those of the International Pharmacopoeia, US Pharmacopoeia, and British Pharmacopoeia, as detailed in the “Supply” section 4 below.
    [Show full text]
  • Magnesium for Constipation
    Magnesium for Constipation What is Magnesium Oxide? Magnesium is a mineral that the body uses to keep the organs functioning, particularly the kidneys, heart, and muscles. Magnesium can be obtained from foods such as green vegetables, nuts, and whole grain products. Though most people maintain adequate magnesium levels on their own, some disorders can lower magnesium levels, such as gastrointestinal disorders like Irritable Bowel Syndrome (IBS). Magnesium helps to increase the amount of water in the intestines, which can help with bowel movements. It may be used as a laxative due to these properties, or as a supplement for magnesium deficiency. What is the dose amount? The maximum dose for Magnesium is 2 grams or 2000 milligrams. You should not take more than 4 tablets or capsules in one day. Magnesium comes in tablets and capsules (500 mg): take orally as directed by your doctor and take with a full 8-ounce glass of liquid. One Tablespoon of Milk of Magnesium is equal to 500 mg. Tablets/Caplets may be taken all at bedtime or separately throughout the day. Side Effects There can be many side effects related to the intake of oral Magnesium. Some of the frequent side effects include diarrhea. You should notify your doctor immediately if you have any of the following severe side effects: black, tarry stools nausea Michigan Bowel Control Program - 1 - slow reflexes vomit that looks like coffee grounds Where can I purchase Magnesium? You can find Magnesium over the counter at most stores that sell supplements and at pharmacies. It typically costs $5 for a 100-count bottle.
    [Show full text]
  • Therapeutic Uses of Magnesium MARY P
    COMPLEMENTARY AND ALTERNATIVE MEDICINE Therapeutic Uses of Magnesium MARY P. GUERRERA, MD, University of Connecticut School of Medicine, Farmington, Connecticut STELLA LUCIA VOLPE, P,hD University of Pennsylvania School of Nursing, Philadelphia, Pennsylvania JUN JAMES MAO, MD, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania Magnesium is an essential mineral for optimal metabolic function. Research has shown that the mineral content of magnesium in food sources is declining, and that magnesium depletion has been detected in persons with some chronic diseases. This has led to an increased awareness of proper magnesium intake and its potential therapeutic role in a number of medical conditions. Studies have shown the effectiveness of magnesium in eclampsia and preeclampsia, arrhythmia, severe asthma, and migraine. Other areas that have shown promising results include lowering the risk of metabolic syndrome, improving glucose and insulin metabolism, relieving symptoms of dysmenorrhea, and alleviat- ing leg cramps in women who are pregnant. The use of magnesium for constipation and dyspepsia are accepted as standard care despite limited evidence. Although it is safe in selected patients at appropriate dosages, magnesium may cause adverse effects or death at high dosages. Because magnesium is excreted renally, it should be used with caution in patients with kidney disease. Food sources of magnesium include green leafy vegetables, nuts, legumes, and whole grains. (Am Fam Physician. 2009;80(2):157-162. Copyright © 2009 American Academy of Family Physicians.) agnesium is the fourth most use (e.g., diuretics, antibiotics); alcoholism; abundant essential mineral and older age (e.g., decreased absorption of in the body. It is distributed magnesium, increased renal exertion).1 approximately one half in the There are challenges in diagnosing mag- Mbone and one half in the muscle and other nesium deficiency because of its distribution soft tissues; less than one percent is in the in the body.
    [Show full text]
  • MAGNESIUM SULFATE Chemical and Technical Assessment
    MAGNESIUM SULFATE Chemical and Technical Assessment Revised by Madduri V. Rao, Ph.D. for the 68th JECFA (Original prepared by Yoko Kawamura, Ph.D. for the 63rd JECFA) 1. Summary Magnesium sulfate was evaluated by the Committee at its 63rd meeting. The outstanding information on functional uses other than nutrient supplement as well as information on commercial use of anhydrous magnesium sulfate and magnesium sulfate was requested for evaluation by the 68th JECFA meeting. Magnesium sulfate is commercially available as heptahydrate, monohydrate, anhydrous or dried form containing the equivalent of 2 - 3 waters of hydration. Magnesium sulfate occurs naturally in seawater, mineral springs and in minerals such as kieserite and epsomite. Magnesium sulfate heptahydrate is manufactured by dissolution of kieserite in water and subsequent crystallization of the heptahydrate. Magnesium sulfate is also prepared by sulfation of magnesium oxide. It is produced with one or seven molecules of water of hydration or in a dried form containing the equivalent of about 2 - 3 waters of hydration. Magnesium sulfate is available as brilliant colourless crystals, granular crystalline powder or white powder with a bitter salty cooling taste. Crystals effloresce in warm, dry air. It is freely soluble in water, very soluble in boiling water, and sparingly soluble in alcohol. Magnesium sulfate is used as a nutrient, firming agent and flavour enhancer. It is also used as a fermentation aid in the processing of beer and malt beverages. No food uses have been identified for the anhydrous form of magnesium sulfate. 2. Description Magnesium sulfate occurs with one (monohydrate), seven (heptahydrate), or no (anhydrous) molecules of water of hydration.
    [Show full text]
  • Anatomical Classification Guidelines V2020 EPHMRA ANATOMICAL
    EPHMRA ANATOMICAL CLASSIFICATION GUIDELINES 2020 Anatomical Classification Guidelines V2020 "The Anatomical Classification of Pharmaceutical Products has been developed and maintained by the European Pharmaceutical Marketing Research Association (EphMRA) and is therefore the intellectual property of this Association. EphMRA's Classification Committee prepares the guidelines for this classification system and takes care for new entries, changes and improvements in consultation with the product's manufacturer. The contents of the Anatomical Classification of Pharmaceutical Products remain the copyright to EphMRA. Permission for use need not be sought and no fee is required. We would appreciate, however, the acknowledgement of EphMRA Copyright in publications etc. Users of this classification system should keep in mind that Pharmaceutical markets can be segmented according to numerous criteria." © EphMRA 2020 Anatomical Classification Guidelines V2020 CONTENTS PAGE INTRODUCTION A ALIMENTARY TRACT AND METABOLISM 1 B BLOOD AND BLOOD FORMING ORGANS 28 C CARDIOVASCULAR SYSTEM 35 D DERMATOLOGICALS 50 G GENITO-URINARY SYSTEM AND SEX HORMONES 57 H SYSTEMIC HORMONAL PREPARATIONS (EXCLUDING SEX HORMONES) 65 J GENERAL ANTI-INFECTIVES SYSTEMIC 69 K HOSPITAL SOLUTIONS 84 L ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS 92 M MUSCULO-SKELETAL SYSTEM 102 N NERVOUS SYSTEM 107 P PARASITOLOGY 118 R RESPIRATORY SYSTEM 120 S SENSORY ORGANS 132 T DIAGNOSTIC AGENTS 139 V VARIOUS 141 Anatomical Classification Guidelines V2020 INTRODUCTION The Anatomical Classification was initiated in 1971 by EphMRA. It has been developed jointly by Intellus/PBIRG and EphMRA. It is a subjective method of grouping certain pharmaceutical products and does not represent any particular market, as would be the case with any other classification system.
    [Show full text]
  • Estonian Statistics on Medicines 2013 1/44
    Estonian Statistics on Medicines 2013 DDD/1000/ ATC code ATC group / INN (rout of admin.) Quantity sold Unit DDD Unit day A ALIMENTARY TRACT AND METABOLISM 146,8152 A01 STOMATOLOGICAL PREPARATIONS 0,0760 A01A STOMATOLOGICAL PREPARATIONS 0,0760 A01AB Antiinfectives and antiseptics for local oral treatment 0,0760 A01AB09 Miconazole(O) 7139,2 g 0,2 g 0,0760 A01AB12 Hexetidine(O) 1541120 ml A01AB81 Neomycin+Benzocaine(C) 23900 pieces A01AC Corticosteroids for local oral treatment A01AC81 Dexamethasone+Thymol(dental) 2639 ml A01AD Other agents for local oral treatment A01AD80 Lidocaine+Cetylpyridinium chloride(gingival) 179340 g A01AD81 Lidocaine+Cetrimide(O) 23565 g A01AD82 Choline salicylate(O) 824240 pieces A01AD83 Lidocaine+Chamomille extract(O) 317140 g A01AD86 Lidocaine+Eugenol(gingival) 1128 g A02 DRUGS FOR ACID RELATED DISORDERS 35,6598 A02A ANTACIDS 0,9596 Combinations and complexes of aluminium, calcium and A02AD 0,9596 magnesium compounds A02AD81 Aluminium hydroxide+Magnesium hydroxide(O) 591680 pieces 10 pieces 0,1261 A02AD81 Aluminium hydroxide+Magnesium hydroxide(O) 1998558 ml 50 ml 0,0852 A02AD82 Aluminium aminoacetate+Magnesium oxide(O) 463540 pieces 10 pieces 0,0988 A02AD83 Calcium carbonate+Magnesium carbonate(O) 3049560 pieces 10 pieces 0,6497 A02AF Antacids with antiflatulents Aluminium hydroxide+Magnesium A02AF80 1000790 ml hydroxide+Simeticone(O) DRUGS FOR PEPTIC ULCER AND GASTRO- A02B 34,7001 OESOPHAGEAL REFLUX DISEASE (GORD) A02BA H2-receptor antagonists 3,5364 A02BA02 Ranitidine(O) 494352,3 g 0,3 g 3,5106 A02BA02 Ranitidine(P)
    [Show full text]
  • Electrolytes: Enteral and Intravenous – Adult – Inpatient Clinical Practice Guideline
    Electrolytes: Enteral and Intravenous – Adult – Inpatient Clinical Practice Guideline Note: Active Table of Contents – Click each header below to jump to the section of interest Table of Contents INTRODUCTION .................................................................................................................................. 6 DEFINITIONS ....................................................................................................................................... 6 RECOMMENDATIONS ........................................................................................................................ 7 1. POTASSIUM (K+) ............................................................................................................................. 7 3- 2. PHOSPHATE (PO4 ) ........................................................................................................................ 9 3. MAGNESIUM (MG2+) ...................................................................................................................... 10 4. CALCIUM (CA2+) ............................................................................................................................ 12 5. SLIDING SCALE ELECTROLYTES ............................................................................................... 14 METHODOLOGY ............................................................................................................................... 15 COLLATERAL TOOLS & RESOURCES ..........................................................................................
    [Show full text]
  • Serum Magnesium Concentration in Children with Asthma
    Original Investigation Eurasian J Pulmonol 2014; 16: 36-9 Serum Magnesium Concentration in Children with Asthma Nevin Hatipoğlu1, Hüsem Hatipoğlu1, Özden Türel2, Çiğdem Aydoğmuş1, Nuri Engerek1, Serdar Erkal3, Rengin Şiraneci1 1Clinic of Peditrics, Kanuni Sultan Süleyman Education and Research Hospital, İstanbul 2Department of Pediatrics, Bezmialem Vakif University Faculty of Medicine, İstanbul 3Biochemistry Laboratory, Kanuni Sultan Süleyman Education and Research Hospital, İstanbul Abstract Objective: Asthma is the most common chronic disease of childhood, and magnesium is one of the most frequently found minerals in human body and it is used in the treatment of asthma. Although there are studies on magnesium levels in adult patients with asthma, there is yet no data on the lev- els of magnesium in children. The present study compared the levels of serum magnesium between the children with asthma and healthy children. Methods: Children aged between 5 and 17 years with mild-moderate persistent asthma, who were admitted to our hospital between January 2009 and August 2010, were included in the study. Serum magnesium levels were measured in 50 patients with acute asthma attack, in 50 patients receiving treatment for stable asthma, and in 50 children admitted to the hospital for any reason and matched with asthma patients except for the diagnosis of asthma. The test was performed by photometric method using Roche-Hitachi Modular P biochemistry analyzer. The normal range of serum Mg was considered to be 1.59-to-2.10 mg/dL and p<0.05 was considered statistically significant. Results: All three groups were similar in terms of mean age and gender distribution.
    [Show full text]
  • The Selection and Use of Essential Medicines
    WHO Technical Report Series 958 THE SELECTION AND USE OF ESSENTIAL MEDICINES This report presents the recommendations of the WHO Expert THE SELECTION AND USE Committee responsible for updating the WHO Model List of Essential Medicines. The fi rst part contains a review of the OF ESSENTIAL MEDICINES report of the meeting of the Expert Subcommittee on the Selection and Use of Essential Medicines, held in October 2008. It also provides details of new applications for paediatric medicines and summarizes the Committee’s considerations and justifi cations for additions and changes to the Model List, including its recommendations. Part Two of the publication is the report of the second meeting of the Subcommittee of the Expert Committee on the Selection and Use of Essential Medicines. Annexes include the revised version of the WHO Model List of Essential Medicines (the 16th) and the revised version of the WHO Model List of Report of the WHO Expert Committee, 2009 Essential Medicines for Children (the 2nd). In addition there is a list of all the items on the Model List sorted according to their (including the 16th WHO Model List of Essential Medicines Anatomical Therapeutic Chemical (ATC) classifi cation codes. and the 2nd WHO Model List of Essential Medicines for Children) WHO Technical Report Series — 958 WHO Technical ISBN 978-92-4-120958-8 Geneva TTRS958cover.inddRS958cover.indd 1 110.06.100.06.10 008:328:32 The World Health Organization was established in 1948 as a specialized agency of the United Nations serving as the directing and coordinating authority for SELECTED WHO PUBLICATIONS OF RELATED INTEREST international health matters and public health.
    [Show full text]