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ACKNOWLEDGMENTS This work was supported in part by the following Public Health Service grants: 2U01AI32906, 1P20RR11126, G12-RR03051, AI34858, R25-GM61838 to M.M. ; , and R01AI39191 to J.F.R. ; . We acknowledge the technical assistance of Ileana Feliciano.

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GERD with risk of recurrent aspiration pneumonia in the elderly Aciphex: dosed at 20mg daily Nexium: dosed up to 40mg daily Prevacid: dosed up to 60mg daily Prilosec omeprazole: dosed up to 40mg daily Protonix: dosed at 40mg daily Hypersecretory Conditions: ie-Zollinger-ellison Aciphex: dosed at 60mg daily up to 60mg twice a day ; Prevaicd: dosed at 60mg daily up to 90mg twice a day ; Prilosec omeprazole: dosed at 60mg daily up to 120mg three times a day ; Barrett's esophagitis: Aciphex: dosed at 20mg daily Nexium: dosed at 20mg daily Prevacid: dosed at 30mg daily Prilosec omperazole: dosed at 20mg daily Protonix: dosed at 40mg daily Clients who have failed H2Blocker therapy: Aciphex: dosed at 20mg daily Nexium: dosed at 20mg daily Prevacid: dosed at 30mg daily Prilosec omperazole: dosed at 20mg daily Protonix: dosed at 40mg daily Clients with G-tubes: Prevacid: dosed at 30mg daily Prilosec omperazole: dosed at 20mg daily Omeprazole may be approved in place of Prevacid if noted Prevacid has failed or clogs up tubes. NG tubes: may open up prevacid capsule and mix intact granules with 40ml of apple juice, then inject in NG tube ; Prevacid Suspension will be reserved for clients less than 12 years of age and clients who have difficulty swallowing. Prior authorization will be denied for clients who have tube feeds. Ptotonix Intravenous: A PA is required. Must be given in the patient's home or in a longterm care facility.
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Proton-pump inhibitors PPIs ; are a class of antisecretory compounds that suppress gastric acid secretion and are generally recognized as the most potent acid suppressants available.1 Parietal cells line the gastric mucosa and secrete acid into the gastric lumen in response to several stimuli. Within the parietal cell, a gastric transport enzyme known as hydrogen potassium adenosine triphosphatase H + K -exchanging ATPase ; is involved in the final step in acid secretion. This enzyme, commonly referred to as the proton pump, exchanges potassium ions K + ; for hydrogen ions H + ; resulting in a lower gastric pH. PPIs exert their effect by covalently binding to the proton pump and irreversibly inhibiting this ion exchange, causing an increase in gastric pH. PPIs will only inhibit proton pumps that are actively secreting acid.1 Following a meal approximately 70%-80% of the proton pumps will be active.2 Thus single doses of PPIs will not completely inhibit acid secretion and subsequent doses are required to inhibit previously inactive proton pumps and newly regenerated pumps. With regular dosing, maximal acid suppression occurs in 3-4 days.1-3 Currently, there are 5 PPIs available in a variety of formulations. They include esomeprazole, lansoprazole, omeprazole, pantoprazole, and rabeprazole. All 5 PPIs are substituted benzimidazole derivatives and are structurally related. Omeprazole is a racemic mixture of S- and R-isomers and esomeprazole represents a formulation that contains only the S-isomers of omeprazole. Following oral administration, the S-isomer has demonstrated higher plasma levels compared to the R-isomer. Primary differences between the PPIs occur in their pharmacokinetic and pharmacodynamic properties along with formulation availability. One PPI formulation, Prilosec OTC, is available over-the-counter OTC ; . All other PPI formulations require a prescription.4-12 The single entity proton-pump inhibitors that are included in this review are listed in Table 1. This review encompasses all dosage forms and strengths. Table 1. Single Entity Proton-pump Inhibitors Included in this Review Generic Name s ; Formulation s ; Example Brand Name s ; esomeprazole delayed-release capsule, Nexium, Nexium injection I.V. lansoprazole delayed-release capsule, Prevacid, Prevacid delayed-release granules IV for oral suspension, delayed-release orally disintegrating tablet, injection omeprazole delayed-release capsule Prilosec * omeprazole magnesium delayed-release tablet Prilosec OTC omeprazole and sodium capsule, packet Zegerid bicarbonate pantoprazole delayed-release tablet, Protonix, Pdotonix injection IV rabeprazole delayed-release tablet Aciphex. NDA 20-987 S-022 Page 17 Pathological Hypersecretory Conditions Including Zollinger-Ellison Syndrome The dosage of PROTONIX in patients with pathological hypersecretory conditions varies with the individual patient. The recommended adult starting dose is 40 mg twice daily. Dosage regimens should be adjusted to individual patient needs and should continue for as long as clinically indicated. Doses up to 240 mg daily have been administered. Some patients have been treated continuously with PROTONIX for more than 2 years. No dosage adjustment is necessary in patients with renal impairment, hepatic impairment, or for elderly patients. Doses higher than 40 mg day have not been studied in hepatically-impaired patients. No dosage adjustment is necessary in patients undergoing hemodialysis. PROTONIX delayed-release Tablets should be swallowed whole, with or without food in the stomach. If patients are unable to swallow a 40 mg tablet, two 20 mg tablets may be taken. Concomitant administration of antacids does not affect the absorption of PROTONIX. Patients should be cautioned that PROTONIX delayed-release Tablets should not be split, chewed or crushed. HOW SUPPLIED PROTONIX pantoprazole sodium ; Delayed-Release Tablets are supplied as 40 mg yellow oval biconvex delayed-release tablets imprinted with PROTONIX brown ink ; on one side. They are available as follows: NDC 0008-0841-10 bottles of 100 NDC 0008-0841-81 bottles of 90 NDC 0008-0841-91 bottles of 1000 NDC 0008-0841-99 carton of 10 Redipak blister strips of 10 tablets each PROTONIX is supplied as 20 mg yellow oval biconvex delayed-release tablets imprinted with P20 brown ink ; on one side. They are available as follows: NDC 0008-0843-81 bottles of 90 Storage Store PROTONIX delayed-release Tablets at 2025C 6877F excursions permitted to 1530C 59-86F ; . [See USP Controlled Room Temperature]. U.S. Patent No. 4, 758, 579 and bentyl. Studies continue to show that the simple use of a multivitamin can decrease risk of quite a number of birth defects besides the well-documented neural tube defects of spina bifida and anencephaly. For example, periconceptional intake of thiamine, niacin and pyridoxine seems to contribute to the prevention of oral-facial clefts. A multivitamin will also decrease risk of birth defects associated with vitamin B12 deficiency, which has been shown to occur in unsupplemented vegans and also surprisingly ; among people with gastroesophageal reflux problems GERD ; who use medications that decrease stomach acid production such as Prilosec, Prevacid , Nexium, Protoni and others. ; Low stomach acid production impairs absorption of vitamin B12 from food, but it is easily corrected by providing the crystalline form of vitamin B12 found in vitamin supplements. Glucophage Metformin ; is a medication for diabetes that has been shown to negatively affect absorption of vitamin B12.[For more information on these issues, please see "Aunt Cathy's Guide to Nutrition: New Discoveries about Folic Acid and Health." And "Aunt Cathy's Guide to Nutrition: a Vitamin B12 Update."] Folic acid supplementation, fortification and or multivitamin supplementation has been associated with significant reduction of risk for many anomalies besides neural tube defects. 1 ; incidence of all birth defects overall; 2 ; cardiovascular anomalies, 3 ; orofacial clefts; 4 ; limb deficiencies ; 5 ; urinary tract defects; 6 ; nonsyndromic omphalocele; and 7 ; imperforate anus.
Both the quantity and quality of dietary fat have been implicated in the incidence of colon cancer 7-10 ; . Although several mechanisms have been offered to explain the role of dietary fat in the de velopment of cancer, the exact mechanism is still not known. One of the possible mechanisms is that the activation of PLAj by dietary fat modulates the ac tivity of PKC and thus affects the development of colon cancer. Another possibility is that dietary fat may influence the structure of the plasma membranes of colonocytes, which may influence the activity of PKC because PKC binds to the membranes on acti vation 3, 4 ; . The present study was conducted to examine the effect of dietary lipid content and com position on the activity of microsomal PLAj in the large intestinal tract mucosa of the rat. The oils used in the diet to alter the fatty acid composition were either safflower oil [ n-6 ; fatty acid rich] or menhaden oil [ n-3 ; fatty acid rich]. In these studies, the enzyme activity was measured in three different locations of the rat intestinal tract: cecum, proximal colon and distal colon and zantac. Arkinson's disease is one of the most disabling chronic neurologic diseases and leads to a significant loss of quality of life.1, 2 Several drugs are available that can effectively treat the symptoms of the disease, but longterm medical management is often complicated by the appearance of levodopa-induced motor complications, leading to rapid changes between periods of severe akinesia and periods of mobility that may be accompanied by troublesome hyperkinesias.3 Dopamine agonists, amantadine, catechol O-methyltransferase COMT ; inhibitors, 3 and other drugs can effectively improve mobility and reduce dyskinesias initially but typically fail after several years.4 The administration of high-frequency continuous electrical stimulation to the subthalamic nucleus through a surgically implanted device has been shown to improve motor symptoms in patients with advanced stages of Parkinson's disease.5, 6 In open follow-up studies, mobility was significantly improved, and dyskinesias were dramatically reduced for up to five years.7 However, this therapy will be acceptable to patients only if the symptomatic benefits are greater than the inherent surgical risks and reduce the burden of disease more effectively than optimal drug therapy. Parkinson's disease interferes with various aspects of the quality of life, particularly those related to physical and social functioning.1, 2 We performed a randomized, controlled trial comparing neurostimulation with the best medical management over a six-month period. Changes in the quality of life and motor function, the latter assessed while the patient was not receiving medication, were the primary outcome measures. Topics: personal experience , health , injuries , recovery asked by: shariculaw - 6 months ago send a compliment ; please sign in to give a compliment and carafate. Then my cardiologist put me on slo-mag time release magnesium ; and it did wonders for the chest pains i was getting. They are available as follows: NDC 0008-0841-10 bottles of 100 NDC 0008-0841-81 bottles of 90 NDC 0008-0841-91 bottles of 1000 NDC 0008-0841-99 carton of 10 Redipak blister strips of 10 tablets each PROTONIX is supplied as 20 mg yellow oval biconvex delayed-release tablets imprinted with P20 brown ink ; on one side. They are available as follows: NDC 0008-0843-81 bottles of 90 NDC 0008-0843-99 carton of 10 Redipak blister strips of 10 tablets each and metoclopramide.

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Rogress in understanding the life cycle of the HIV virus has led to development of drugs that target five vital processes used by HIV to invade and take over CD4-positive cells, most of which are intracellular. Investigations into an extracellular target for treatment, the attachment and entry of HIV to cells, has resulted in production of two drugs that can interfere with viral attachment, enfuvirtide Fuzeon ; and more recently, maraviroc. Entry of HIV into CD4-bearing lymphocytes and monocytes requires several steps: a ; binding of part of the virus' envelope gp 120 ; to the CD4 receptor; this results in b ; a change in the shape of the gp 120, revealing a previously-hidden binding site for chemokine co-receptors CCR5 and CXCR4 ; , followed by c ; interaction of the gp 120 with one of two co-receptors, CCR5 or CXCR4, and and allopurinol.

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Substances in the poisons list are subject to the Chemicals Hazard Information and Packaging for Supply ; Regulations Northern Ireland ; 2002 and must be supplied in an appropriate container. The container of any poison must be impervious to the poison and sufficiently stout to prevent leakage arising from the ordinary risks of handling and transport. The outer surface of a bottle, if of no greater capacity than 1.14 litres, used for the sale or supply of a liquid poison must be fluted vertically with ribs or grooves recognisable by touch. This requirement applies to bottles made of any material. It does not apply to the sale or supply of poisons to be exported to purchasers outside the United Kingdom, or the sale or supply to a person or institution concerned with scientific education or research or chemical analysis, for the purpose of that education or research or analysis. Pharmacists should refer to the requirements of the Chemicals Hazard Information and Packaging for Supply ; Regulations Northern Ireland ; 2002 with respect to containers for poisons see section 5 and ranitidine.

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Barrier Embarrassment Hard to understand genital herpes Too little time Provider not sympathetic Provider not like me Provider different gender Provider different age Provider different race and isolation eight ; , discuss preventing transmission to a partner seven ; and, in general, have non-judgemental communications six ; . Frequency % ; 223 56.6 ; 99 25.1 ; 94 23.9 ; 75 19.0 ; 36 9.1 ; 36 9.1 ; 29 7.4 ; 16 4.1 ; education counselling occupied less than 11 minutes of clinic time. Given the numerous issues raised by a chronic STD such as genital herpes including partner disclosure, questions about preventing transmission and the potential need for suppressive therapy an International Herpes Management Forum consensus panel has recommended that all newly diagnosed patients be offered a follow-up visit after the initial diagnosis.10 Study results indicated that only 44.3% of patients reported any follow-up visit. Also of interest was the reported content covered, and the recommended content to discuss. An ASHA survey published in 19939 showed that patients were most satisfied with the counselling they received on clinical topics such as treatment and least satisfied with counselling on the psychosocial impact of herpes or its impact on sexual relationships. Patient responses demonstrated that clinical topics e.g. treatment, transmission, natural history ; were the most likely to have been covered, while the least likely were psychosocial issues e.g. emotional impact, risk reduction, effect on sexual relationships ; . Interestingly, once a topic was covered, patient levels of satisfaction were quite high for all 13 counselling topics listed on.

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Increased potassium can be related to skin infection, if severe enough and zyloprim. Exforge was also evaluated for safety in a 6-week, double-blind, active-controlled trial of 130 hypertensive patients with severe hypertension mean baseline BP of 171 113 mmHg ; . Adverse events were similar in patients with severe hypertension and mild moderate hypertension treated with Exforge. A wide age range of the adult population, including the elderly was studied range 19-92 years, mean 54.7 years ; . Women comprised almost half of the studied population 47.3% ; . Of the patients in the studied Exforge group, 87.6% were Caucasian. Black and Oriental patients each represented approximately 4% of the population in the studied Exforge group.

Prilosec OTCTM * , omeprazole * , Protoinx Zithromax * Lopid * , Questran * , Niaspan Maxalt, Imitrex Oral Zovirax * Benefit exclusion Risperdal, Seroquel Generic over-the-counter Loratadine is covered with a physician's prescription. Generic over-the-counter Loratadine is covered with a physician's prescription and proventil and Buy protonix.

There were 19 studies with 3, 819 impotent men, ranging in size from 10 to 800 men. Studies usually had a wide age range, with mean age from 35 to 61 years. In 16 of the 19 studies, smoking rates in impotent men were higher than those in the general male population. Overall the age and location matched smoking prevalence in men was 28%. In impotent men it was 40%, a significant difference of 12% 95% confidence interval 11 to 14% ; . This paper alone does not constitute a definitive link between smoking and impotence in men. But it does go a long way to making the claim, and in the end it may be more influential in terms of making young men think twice about starting smoking, and make older men think about giving it up. Women may also appreciate the information. There are at least two systematic reviews of smoking and erectile dysfunction published recently. The bottom line from these is that smoking doubles the risk of erectile dysfunction in men. Erectile problems are common in men, affecting 10-25%. All the evidence may not yet be in, but men might like to work on the basis that smoking will exacerbate a problem that age and chronic disease will bring to their door at some time. 200 Allergic Reaction to Epidural Methylprednisolone Acetate Andrew Linn, MD Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215 Jyotsna Nagda, MD Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215 We present a case of allergic reaction to methylprednisolone acetate. To date, there have been approximately 100 published reports of immediate hypersensitivity reactions occurring after oral and intravenous administration of corticosteroids 1 we could not find a reported case of hypersensitivity reaction caused after epidural administration of steroids. A 32 year-old female with a history of low back pain, RLE radiculopathy, presented to the pain clinic for her first lumbar epidural steroid injection. Her past medical history included gastroesophageal reflux, and congenital lack of sexual organs. An uneventful intralaminar lumbar epidural steroid injection was performed under fluoroscopic guidance with 3 cc's of 1% lidocaine and 80 mg of methylprednisolone acetate. Approximately 30 minutes after receiving the LESI, the patient began to develop erythema, generalized pruritus, tightness in her chest, and swelling of her throat. The angioedema did not compromise her breathing, though it did prompt her to go to emergency department, where she was treated with diphenhydramine and intravenous fluids, with resolution of her symptoms. She later underwent skin prick testing cutaneous allergic testing ; with methylprednisolone acetate, dexamethasone, and kenalog, and had immediate positive response to the first two. She was also tested for sensitivity to local anesthetics, and failed to respond to lidocaine or other amide local anesthetics. The positive skin prick test suggests an IgE mediated hypersensitivity reaction to methylprednisolone acetate. Hypersensitivity reactions to topical steroid preparations are common: approximately 5 percent of those who use steroid creams develop sensitivity reactions. Adverse reactions to systemic steroids has been reported as 0.3%, with water soluble succinate esters of methylprednisolone and hydrocortisone the more common provocateurs 1 ; . It less common for hydrophobic steroid formulations to promote a hypersensitivity reaction, though there have been cases of intra-articular injections causing urticaria, angioedema, and cardiovascular collapse 2-5 ; . References 1. Kamm GL, Hagmeyer KO. Allergic-type reactions to corticosteroids. Ann Pharmacother. 1999; 33: 451-60. Pollock B, Wilkinson SM, MacDonald-Hull SP. Chronic urticaria associated with intraarticular methylprednisolone. Brit J Dermatol 2001; 144: 1228-1230. Karsh J, Yang WH. An anaphylactic reaction to intraarticular triamcinolone: a case report and review of the literature. Ann Allergy Asthma Immunol 2003; 90: 254-8. Mace S, Vadas P, Pruzanski W. Anaphylactic shock induced by intraarticular She had a previous allergic reaction to Peotonix injection on methylprednisolone acetate. J Rheumatol 1997; 24: 1191-4. Clifford RE, Baskin MN, Novoseletsky D, Speech D, Patel R. Flushing as a side effect following lumbar transforaminal epidural steroid injection. Pain Phys 2004; 7: 427-429. Targeted Cervical Epidural Steroid Injection Using a Radiopaque Catheter--A Technique Report Muhammad Khan University of Cincinnati, Cincinnati, OH 45609 Ryan Zollett University of Cincinnati, Cincinnati, OH 45609 David Okano University of Cincinnati, Cincinnati, OH 45609 Muhammad Munir University of Cincinnati, Cincinnati, OH 45609 Introduction: Cervical radicular pain is most commonly caused by disc herniation or foraminal stenosis. Cervical epidural steroid injections have been employed in the treatment successfully for their anti-inflammatory effects. The results of such epidural injections depend on precise and prednisolone.
Express Scripts is the pharmacy benefit manager for your prescription drug benefit plan. If you have any questions about your prescription drug benefits, contact Express Scripts toll free at 877 ; 828-9744 TDD: 800 ; 855-2881 ; . The following information replaces the second paragraph of text as well as the chart located in the Express Scripts section on page 7 of the 2005 Series 2 benefit update: One of the ways your plan maintains coverage of quality cost-effective medications is a multi-tier copayment pharmacy benefit. Effective July 1, 2006, copayments for omeprazole generic Prilosec ; will decrease. Copayments will increase for non-preferred brand name drugs purchased through home delivery mail order ; . The following chart illustrates your copayment based on the type of prescription you fill and where you get it filled.Part II Copayment for: Tier 1: Generic Drugs All generic drugs except: omeprazole acid reducer ; Value Tier generics Also covered: Prilosec OTC 28-day supply retail; 84-day supply mail ; * Tier 2: Preferred Brand Name Drugs All preferred brand name drugs and: omeprazole acid reducer ; Tier 3: Non-Preferred Brand Name Drugs All non-preferred brand name drugs including: COX-2 inhibitors pain and inflammation Celebrex ; Brand name proton pump inhibitors acid reducers currently Aciphex, Nexium, Prilosec, Prevacid, Protonix ; Value Tier Generic statin cholesterol lowering lovastatin ; Generic H-2 antagonists acid blockers cimetidine 300, 400 and 800mg; famotidine 40mg; nizatidine 150 and 300mg; ranitidine 300mg.

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Proton-pump inhibitors PPIs ; are even stronger acid-reducing medications. They work by significantly reducing the stomach's production of acid and are often more effective than H2 blockers. Usually, only a single pill is required daily. Examples of PPIs include omeprazole Prilosec ; , lansoprazole Prevacid ; , rabeprazole Aciphex ; , pantoprazole Protonix ; , and esomeprazole Nexium ; . Long-term suppression of stomach acid with PPIs helps to prevent recurrence of symptoms. The prescribed dose may vary depending on the severity of symptoms. Long-term use of PPIs is generally effective and safe. Clinical programme Centering on HIV medicine, this is the programme that specializes in the delivery of direct services to people living with HIV AIDS. The services form a continuum from hotlines, voluntary counselling and testing VCT ; , medical treatment and consultation, nursing care, psychosocial support to referrals. The programme also includes the following clinical activities dermatology, genitourinary medicine, hepatitis B vaccination for health care workers, infection control, and management of needlestick injuries. HIV prevention and health promotion programme This is the programme that addresses HIV prevention in the community setting. There are four main activity areas: communication and information, targeted prevention, promoting acceptance and capacity-building. While the main focus is HIV AIDS, there is also involvement in viral hepatitis, STD and bloodborne infections in the health care setting. The characteristics of the programme are its collaborative approach, partnership with the community, and the provision of support to community-based initiatives. Policy development programme This is the programme that supports the functions of the Advisory Council on AIDS ACA ; and its committees, Scientific Working Group on Viral Hepatitis and buy bentyl.
Cyclosporin is a substrate for cytochrome p450 3a4 and the multidrug efflux pump, p-glycoprotein. If we compare 2005 Q4 expenditure with 1993 Q3 the quarter before the 1993 price cut ; , only about 21 per cent of 2005 Q4 expenditure was accounted for by products already sold in 1993 Q3, which were directly affected by the October 1993 price cut. The percentage increases to 51 per cent if all products with the same BNF chemical name as products sold in 1993 Q3 are included, as new formulations and or delivery methods seem to have been significant.3 The extent to which prices of new formulations and or delivery methods are affected by price cuts is uncertain so this analysis suggests that, by the fourth quarter of 2005, between 49 and 79 per cent of branded drug expenditure is unaffected by the 1993 price cut. The comparable figures for the 1999 price cut are 10 to 34 per cent. These figures suggest the percentage of expenditure unaffected by any price cut after five years of the current agreement could be 8 to per cent, 4 depending on the extent to which the price control constrains the price of new formulations and delivery methods.

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Analysis using a fluorescence-activated cell sorter Coulter EPICS Profile ; Nawa et aL, 1990 ; , 40 to 45~ of cells were in the S and G2 M phases of the cell cycle under the conditions used. After a 1 h adsorption period, serum-free MEM was added, the mixture was incubated at 37 C and, at the indicated times after infection, cells were infected with HSV-1 KOS at a multiplicity of As shown in Fig. l, the size of the dTTP pool increased rapidly after HSV-1 infection, reached a maximum size 6 to 9 post-infection and decreased rapidly thereafter. Both the dCTP and dGTP pools also increased in size during virus infection, but to a lesser extent. There was no significant change in the size of the dATP pool. We next studied the change in the size of the dTTP pool in Vero cells infected with TK- and RR- mutants of HSV-1 KOS. The results are shown in Fig. 2 a ; . Unexpectedly, the size of the dTTP pool of HSV-1 TK- ; -infected cells increased to almost the same extent as that of HSV-l TK + ; -infected cells. Similar results. Symptoms Nausea, no vomiting Vomiting solids occasionally Vomiting solids frequently with normal wt loss ; Causes Normal postop course Dietary noncompliance Dietary noncompliance Anatomic cause Management 1. No Rx Anti-emetics prn 1. Nutrition referral 1. Nutrition referral 2. UGI or EGD 3. Bariatric program referral 1. UGI or EGD 2. Bariatric program referral 1. Protonix 40 po BID, carafate 1gm qid 2. EGD 3. Bariatric prog referral Work up and treatment based on history. Refer to Nutrition and Bariatric program as needed.

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