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INTRODUCTION Neuropathic pain and muscle-related pain associated with neurological disorders, such as multiple sclerosis MS ; , are not always amenable to treatment with conventional analgesic drugs. In addition, some patients may not tolerate existing treatment options well. Patients with MS may also have to contend with muscle spasticity, tremor, impaired bladder control, muscle weakness, dystonia and ataxia, and currently available drugs may not offer adequate control of these symptoms. An agent with a different mode of action to currently available drugs, which can address many of these issues would, therefore, be desirable. Cannabis-based medicinal extracts CBME ; are being investigated as such agents for patients experiencing these problems. The Medical Research Council MRC ; is sponsoring a large study n 667 ; of a natural cannabis oil oral capsule Cannador ; and a synthetic THC oral capsule Marinol ; for the relief of MS symptoms. This is the Cannabinoids in Multiple Sclerosis CAMS ; study and first phase results are due to be made public in September 2003. However, GW Pharmaceuticals submitted a licence application to MHRA in March 2003 for their CBME product, Sativex, for the treatment of the symptoms of MS and neuropathic pain [Personal communication, GW Pharmaceuticals, 19 05 03]. This is a pump action oromucosal spray device that contains 2.7mg THC and 2.5mg CBD per actuation. If licensed, this product will be marketed and distributed in the UK by Bayer plc. This monograph discusses the GW Pharmaceuticals CBME product. are then released slowly over a prolonged period [1]. In one study of 86 chronic cannabis users, some had intermittently positive urine tests for up to 77 days after last smoking cannabis, but with negative tests occurring periodically during that time [2]. The average elimination time in these chronic, heavy users is probably about 4 weeks. It is not clear what the implications of this delayed elimination are for the persistence of any adverse effects or interactions. CBD has a half-life of 2 to 5 days when taken orally [3].
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It has been reported that life expectancy of type-2 diabetics is shortened by about seven years.16 We have a type-2 diabetes epidemic in the US of over 21 million people, plus at least 54 million pre-diabetics. The total direct and indirect cost of diabetes is approximately US$160 billion. One of every five dollars allocated by the National Institutes of Health NIH ; is for diabetes. Diabetes is the most expensive chronic disease with most of the cost spent on the vascular and neurological complications. It is a cardiovascular coronary artery disease risk equivalent. Heart attacks and stroke are two to six times more common. Diabetes is the leading cause of new adult blindness, end-stage renal disease, dialysis, and non-traumatic limb amputations.We know that diabetes accelerates the atherosclerotic process. Arteriosclerotic disease occurs at a younger age, is more widespread, and is more severe.17 Recent surveys indicate that one in every three coronary intensive care patients has diabetes and one of every four hospitalized patients has diabetes. The cost of medication is only about 1011% of total cost.We should be able to prescribe the best medication required to control diabetes and cardiovascular risk factors.The real challenge is to use this information and guidelines to improve diabetes care with a goal of A1C 6%, reduce complications, decrease the cost of diabetes and cardiovascular disease management, improve health, and health-related quality of life.
Cases Related to Hatch-Waxman, Other Collusion Cases . Hatch-Waxman Amendments: A Brief Summary . Brand Name Generic Name Ativan Tranxene lorazepam clorazepate dipostassium . BuSpar buspirone Cardizem CD diltiazem . Cipro ciprofloxacin hydrochloride . Hytrin terazosin hydrochloride . K-Dur-20 potassium chloride . Neurontin gabapentin . Nolvarex tamoxifen citrate . Paxil paroxetine Prilosec omeprazole . Procardia XL extended-release nifedipine . Relafen nabumetome . Taxol paclitaxel . Tiazac diltiazem hydrochloride . Cases Related to Fraud Involving Pricing . Lupron Depot leuprolide . Cases Related to Deceptive Marketing . Claritin loratadine . Coumadin warfarin sodium . Premarin conjugated estrogens . Synthroid levothyroxine . understanding of the Hatch Waxman Amendments to the Federal Food, Drug, and Cosmetic Act1 is necessary in order to appreciate the tactics pharmaceutical companies use to delay and prevent generic competition. A more complete discussion of Hatch Waxman and the drug approval process is covered in a companion piece, Overview of Hatch Waxman: Legislative Background issued by Families USA in April 2002. ; . Congress enacted Hatch Waxman in 1984 in part to facilitate the development and expedite the approval of generic drugs. Hatch Waxman shortened the generic drug approval process by allowing generic manufacturers to file an Abbreviated New Drug Application ANDA ; , incorporating data that the brand name drug manufacturer has already submitted to the FDA. With the ANDA, the generic manufacturer must make one of four certifications to the FDA regarding each patent the brand name manufacturer has submitted to the Orange Book.2 The Orange Book is a publication that lists all prescription drugs approved for use in the U.S. and the patents covering those drugs. The fourth of these certifications, referred to as a Paragraph IV Certification, is the one that has been manipulated by drug manufacturers to extend brand name monopolies. With a Paragraph IV Certification, the generic manufacturer claims that the brand drug patent is invalid or will not be infringed by the generic.3 When a generic manufacturer files a Paragraph IV Certification, it must notify the patent holder for simplicity, referred to here as the brand name drug manufacturer ; . If the brand name drug manufacturer sues the generic manufacturer for patent infringement within 45 days of notice, the FDA cannot issue final approval of that genericor any other generics related to that brand name drugfor 30 months the 30 Month Stay ; unless the patent expires or there is resolution of the lawsuit. The first generic manufacturer filing an ANDA with a Paragraph IV certification is eligible for 180 days, during which time its product will be the only generic on the market the Exclusivity Period ; . The Exclusivity Period starts running either when the generic is commercially marketed or when there is a court decision finding that the patent is either invalid or not infringed by the generic.4 Despite the goal of Hatch Waxman to expand consumer access to generics, the 30 Month Stay and the Exclusivity Period have presented crafty brand name manufacturers with opportunities to extend their monopolies through a variety of anticompetitive tactics. n 30 Month Stay: Since the filing of a patent infringement action within 45 days of notice of a Paragraph IV Certification ANDA delays FDA approval of the generic, brand name manufacturers have an incentive to claim, obtain, and list as many patents as possible. Even a completely frivolous patent infringement action will preclude FDA approval for up to 30 months. This has resulted in brand name manufacturers warehousing as many patents as they can and filing frivolous lawsuits when notified of a Paragraph IV Certification ANDA.

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What about drug therapy? If a better diet and more exercise do not get your cholesterol under control, if you have a strong family history of heart disease, or if your cholesterol is extremely high, you will probably need medication. In fact, drugs are so effective in reducing cholesterol-related deaths that many authorities now recommend them for anyone with high LDL levels. Several types of medications are available.
SMOOT, JOHN MEDLEY, M.D. 07716 ; Batesville, MS 38606 Licensee prohibited from practicing medicine until such time as determination is made that he is able to return to the practice of medicine with reasonable skill and safety to patients. May 28, 1999. The Order of Prohibition effective May 28, 1999, is removed. Licensee may return to the practice of medicine, subject to terms and conditions. August 9, 1999. Consent Order executed in consideration of reinstatement of license, whereby Licensee agrees to certain probationary terms and conditions. August 18, 1999. WARNICK, JAMIE SUE, M.D. 15164 ; Southaven, MS Licensee's practice of medicine shall be restricted to general pediatric care, and Licensee shall be prohibited from performing certain medical care and or procedures, pending the outcome of the scheduled hearing on July 15, 1999. July 2, 1999. Order of Prohibition is removed, and Licensee authorized to return to the practice of medicine subject to certain conditions. July 15, 1999 and orlistat.
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Two years passed. Richard's symptoms weren't getting any worse, and some of them were even beginning to slack off. In my efforts to help, I had prescribed antibiotics, antidepressants, and stimulants. Richard himself explored every conceivable homeopathic option, without appreciable results. I was unable to persuade myself that any of the medications I had prescribed had made a difference, either. It seemed to me that Richard was beginning to get better on his own. By then, his level of activity during any given day hovered at around forty percent of what would have been normal for him. At the start of his illness, I measured Richard's activity level at about twenty percent. Defining a person's activity level in a scientific manner can be complicated, but not impossible. In 1988, two researchers performed a study in which they asked subjects to keep a detailed daily diary in order to calculate the amount of energy expended for every activity. There is a small amount of energy expended for sleep, more for playing the piano, still more for swimming. Using their method, I might have calculated and parlodel. James D. Dannenbaum, Chairman Donald C. Spencer, M.D., Vice Chairman Karen B. Heusinkveld, R.N., Dr.P.H., Secretary F. Diane Barber, R.N. Karen Bonner Audreyjane Castro A. Clare Buie Chaney, Ph.D. Lloyd K. Croft, D.D.S. Carolyn D. Harvey, R.N., Ph.D. Rubye H. Henderson Larry Herrera, M.D. Sue Sandlin Courtney M. Townsend, Jr., M.D. J. Taylor Wharton, M.D. Ex officio Member Chair, Texas Board of Health Debra Stabeno, Designee Executive Director Mickey L. Jacobs, M.S.H.P. Interchange Category: If this medication is ordered. THERAPEUTIC INTERCHANGE: Calcium citrate 21% elemental calcium ; Calcium gluconate 9% elemental calcium ; Calcium lactate 13% elemental calcium ; GENERIC INTERCHANGE: Calcium Carbonate: OSCAL-500 1, 250mg calcium carbonate 500mg elemental ; TUMS various doses TITRALAC various doses TITRALAC PLUS liquid 5-15mL calcium carbonate 500mg, simethicone 20mg 5mL and periactin.
Evista is supposed to have a more powerful gyno blocking effect than nolvadex. Genox nolvadex, tamoxifen ; -without rx 10mg-30 tabs manufacturer pacific generic name: genox genox approved fda rx nolvadex without rx store med's offer tamoxifen rx online-free meds meds breast free rx treat cancer and pioglitazone. 20-jun-2001, # 2 weam join date: apr 2001 745 karmic power: 0 karma hits: -525 there is a very big difference in mechanism between both nolvadex is an anti-estrogen which works by blocking estrogen receptors at the breast tissue arimidex is an anti-aromatase which works by blocking the aromatase enzyme which converts testosterone into estrogen nolvadex do not decrease estrogen concentration in blood therefor it won't decrease or prevent estrogenic side effects as bloating, water retention, blood pressure.
Fig. 6A shows the OR K influx as a function of external K in Na-free medium at different intracellular Na concentrations . It can be seen that internal Na stimulated the OR K influx . As shown in Fig. 6B, the stimulation produced by internal Na involved an FS component of the K influx . Table II shows the kinetic parameters of the FS K influx for the three subjects studied. The Ko.5 for external K ranged from 11 to 23 and was not affected by the internal Na concentration . The V, ax of the FS K influx increased with the elevation of internal Na . The stimulatory effect of internal Na on the FS K influx was half-maximal at 5 mmol liter cell of Na . can be seen in Fig. 6, in Na ; free cells, the OR and FR K influxes were a linear function of external K. In cells containing Na, the FS K influx was a saturable function of the external K concentration . These data indicate that internal Na had a stimulatory role on the Na .-independent K influx and piracetam. Inevitable future progression of disease may not improve outcomes, despite everybody's hopes to the contrary. The second issue that I wanted to get to is duration of treatment. From bone-scan data, at least, we know that early observation of disease status after you begin a new hormone therapy can be misleading, for sure. Bone scans in particular can actually look worse, and we have reasonable evidence that blood test results can spike and fall in response to a new hormone therapy. Three months is a little long for that still to be true, but, again, in a patient with no symptoms, one would be inclined to hold tight and see what the shape of the curve is for the markers. Maybe they are going to spike and drop. DR ABEL: Is there a conflict between the concept of advocating late extended adjuvant therapy and not treating based on tumor markers. Is that conceptually coherent? DR HUDIS: I think so, because the patient population is quite different. In the extended adjuvant setting, overwhelmingly, you're dealing with patients who are cured, so your toxicity profile matters a whole lot. In the metastatic setting, you're palliating, for example, nolvwdex dosing. The side effects of antipsychotic drugs vary greatly and the long term effects are still unknown and piroxicam.

1986 molvadex approved as adjuvant therapy for use alone in postmenopausal women with lymph node-positive early breast cancer. BARR LABS BARR LABS BARR LABS BARR LABS BARR LABS BARR LABS BIRCHWOOD LABS HI-TECH PHARMACAL CORP., INC HI-TECH PHARMACAL CORP., INC and pletal. Anatomy of a billion dollar lie on january 28th, 2004, the us federal drug administration published this press release. ASTHMA: INHALED STEROIDS MAY NOT BE ENOUGH FOR SOME CHILDREN Some children may not be able to keep their asthma under control even if they consistently report using inhaled corticosteroids, a mainstay of asthma treatment. Children with mild to moderate asthma over a one-year period were 20 percent less likely to report having well-controlled asthma compared with those not using any inhaled steroids, a study from researchers at Children's Hospital in boston found. The findings, presented at the American Thoracic Society international Conference in San francisco, held even when the severity of the children's asthma was taken into account. The researchers said it is possible that some children are genetically less responsive to steroids. GREEN TEA: HERBAL AGENTS CAN PREVENT BLADDER INFLAMMATION Herbal agents could be used to treat inflammatory bladder diseases, according to a preliminary study that looked at the ability of green tea to protect bladder cells from inflammation. The study from researchers at the University of Pittsburgh School of Medicine, found catechins--plant metabolites that provide green tea with many anti-oxidative properties--protected normal and cancerous bladder cells from inflammation when researchers exposed the cells to hydrogen peroxide. in a presentation at the American Urological Association in Anaheim, California, the researchers said the results indicate herbal supplements from green tea could be a treatment option for various bladder conditions that are caused by injury or inflammation. SLEEP APNEA: PATIENTS FACE GREATER RISK FOR DEVELOPING DIABETES Patients with obstructive sleep apnea are at increased risk for developing of type ii diabetes, independent of other risk factors, according to researchers at the yale University School of Medicine. in obstructive sleep apnea, the upper airway narrows, or collapses, during sleep. Periods of apnea end with a brief partial arousal that may disrupt sleep up to hundreds of times a night. Obesity is a major risk factor for sleep apnea. in a study presented at the American Thoracic Society 2007 international Conference, the researchers said it is now known exactly what the link is between sleep apnea and diabetes, it is thought that sleep apnea activates the body's fight-orflight response. This triggers a cascade of events, including the production of high levels of the hormone cortisol that ultimately leads to insulin resistance and glucose intolerance, pre-diabetic conditions that, if left untreated, can lead to the development of diabetes. CANCER: ASPIRIN MAY PROTECT AGAINST COLORECTAL DISEASE Aspirin's ability to reduce the risk of colorectal cancer, an association seen in a large number of studies, appears to depend on the drug's inhibition of the COX-2 enzyme, the action that also underlies aspirin's usefulness for treating pain and inflammation. in a study published in the New england Journal of Medicine, investigators from Massachusetts General Hospital, Dana-farber Cancer institute and brigham and women's Hospital reported that regular aspirin intake only reduced the incidence of colorectal tumors that overexpress COX-2. The researchers said an individual who has had colorectal cancer in the past is at higher risk for subsequent tumors, and that might be someone who should discuss the advisability of taking aspirin with his or her primary care physician. They said, however, that current evidence does not support generally recommending aspirin therapy to reduce colorectal cancer risk and premphase and nolvadex, for example, nolvdex prescribing information.

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The usual concentration in which Kollidon VA 64 is used as a binder in tablets and granules lies between 2 % and 5 %. This range is similar to that of Kollidon 30 in tablets. As a typical example of wet granulation Fig. 82 shows that there are no significant differences in the compression diagrams for Kollidon 25, Kollidon 30 and Kollidon VA 64 214.
1. Chabal C, Erjavec MK, Jacobson L et al. Prescription opiate abuse in chronic pain patients: Clinical criteria, incidence, and predictors. Clin J Pain 1997; 13: 150-155. Atluri S, Sudarshan G. A screening tool to determine the risk of prescription opioid abuse among patients with chronic nonmalignant pain. Pain Physician 2002; 5: 447-448. Manchikanti L, Brown K, Singh V. National All Schedules Prescription Electronic Reporting Act NASPER: Balancing substance abuse and medical necessity in interventional pain management. Pain Physician 2002; 5: 294-319. Hill CS. When will adequate pain treatment be the norm? JAMA 1995; 274: 18811882. Dahl JL. Improving the practice of pain management. JAMA 2000; 284: 2785. Hoffmann DE. Pain management and palliative care in the era of managed care: Issue for health insurers. J Law, Med & Ethics 1998; 26: 267-289. Cleeland CS, Gonin R, Hatfield AK et al. Pain and its treatment in outpatients with metastatic cancer. N Engl J Med 1994; 330: 592-596. Joranson DE, Carrow GM, Ryan KM et al. Pain management and prescription monitoring. J Pain Symptom Manage 2002; 23: 231-238. Portenoy RK. Opioid therapy for chronic nonmalignant pain: Clinicians' perspective. J Law Med Ethics 1996; 24: 296-309. Pappagallo M, Heinberg LJ. Ethical issues in the management of chronic nonmalignant pain. Semin Neurol 1997; 17: 203211. Model Guidelines for the Use of Controlled Substances for the Treatment of Pain. Federation of State Medical Boards of the United States, Inc., May 1998. Glajchen M. Chronic pain: Treatment barriers and strategies for clinical practice. J Board Fam Pract 2001; 14: 211-218. American Pain Society. Chronic Pain in America: Roadblocks to Relief. Available at: : ampainsoc . 19 and propranolol.

See A. Towse, What are the short and long run implications for the UK of parallel trade in pharmaceuticals?, Working Paper, London, Office of Health Economics, 1-20. Average expenditure on health, in percentage of GDP, differs by about 20% between the former EU-15 and the accession States former EU-15 8% of GDP; accession states 6.5% ; . In nominal terms, this translates into an average health expenditure per capita in the eight acceding countries, without Cyprus and Malta, of approximately 18% of the average health expenditure per capita in the former EU-15. There are also clear differences between individual acceding countries. While Slovenia is by far the richest country, with a GDP per capita of 16, 000 i.e. approximately 50% above the accession countries' average ; , Latvia's GDP per capita is almost 50% below the accession countries' average. Kanavos, Panos, Joan Costa-i-Font, Sherry Merkur, and Marin Gemmill, The Economic Impact of Pharmaceutical Parallel Trade in European Union Member States: A Stakeholder Analysis, Special Research Paper 2004 ; , LSE Health and Social Care. See Danzon, supra.
Otoxicity of RSG, and the lack of in vivo genotoxicity data in particular, the present study was designed to evaluate whether this drug can cause DNA damage in the hepatocytes and peripheral blood lymphocytes of treated rats. DNA damage was measured using the single cell gel electrophoresis assay Comet assay ; , a method that is used widely for the detection of DNA damage both in vivo and in vitro [Tice et al., 2000; Hartmann et al., 2003]. These are not all the possible side effects of nolvadex. From Austria and Germany report the combined findings of the Austrian Breast and Colorectal Cancer Study Group trial 8 ABCSG trial 8 ; and the Arimidex Nolvadxe 95 trial ARNO 95 ; . The trials involved more than 3, 000 women who received standard treatment for early-stage breast cancer lumpectomy plus radiation or mastectomy ; followed by tamoxifen. After 2 years on the drug, 1, 608 women were randomized to continue tamoxifen, and 1, 618 were assigned to switch to anastrozole. After median follow up of 28 months, the researchers reported a 40% decrease in risk of local or distant metastasis or contralateral breast cancer in the women who took anastrozole compared with the tamoxifen group. In absolute terms, anastrozole conferred a 3.1% eventfree survival benefit over tamoxifen 95.8% versus 92.7% ; . There was no significant difference in overall survival between the groups after 3 years. As expected, however, the drugs did have different side effects. Women on anastrozole experienced significantly more bone fractures odds ratio [OR] 2.14 ; and significantly fewer thromboses OR 0.25 ; than women on tamoxifen. Women on anastrozole also reported more bone pain and nausea. Lead author Raimund Jakesz, MD, of the Vienna Medical University, says the findings support those of earlier trials--in particular the Arimidex, Tamoxifen, Alone or in Combination ATAC ; trial--that found aromatase inhibitors superior to tamoxifen for preventing recurrences, particularly in the first 2 years of therapy. They also suggest that women who have taken 2 to 3 years of tamoxifen therapy should be switched to an aromatase inhibitor for their remaining years of hormonal treatment. That group of patients is likely getting smaller, said Christy Russell, MD, of the University of Southern California's Norris Comprehensive Cancer Center. Russell was not involved in the new research. She serves as. If you already have breast cancer, talk with your doctor about how the benefits of treating breast cancer with nolvadex compare to the risks that are described in this document and orlistat.
There are no data to support the use of nolvadex other than for 5 years see clinical pharmacology - clinical studies - reduction in breast cancer incidence in high risk women.

PUBLICATIONS: a Articles in Refereed Journals : Francis GS, Bonni A, Shen Hechtman P, Yamout B, Carpenter S, Karpati G, Chang PL. Metachromatic leukodystrophy: multiple nonfunctional and pseudodeficiency alleles in a pedigree: problem with diagnosis and counseling. Ann Neurol, 34: 212-218, 1993. Yamout B, Farhat W, Nuweihed I, Hushaymi I. Changes in migraine's symptoms from childhood to adolescence. European Neurology, 36: 174-176, 1996. Yamout B, Nassar N, Ghayyad E, Habbal A. Neurobrucellosis: Clinical presentation, treatment and outcome in seven cases. Accepted for publication in the Mediterranean Journal of infectious and Parasitic Diseases, 11: 111-115, 1996. Yamout B, Zaytoun G, Nuweihed I. The role of facial nerve conduction studies and electromyography in predicting the outcome of Bell's Palsy. Accepted for publication in the European Journal of Neurology, 4: 1-4, 1997. Yamout B, Tayyim A, Farhat W. Meralgia paresthetica as a complication of laparoscopic cholecystectomy. Clinical neurology and neurosurgery, 96: 143-144, 1994. Khalil A, Yamout B, Tabbal S, Salem Z, Mroueh A. Case report and review of literature: leptomeningeal relapse in epithelial ovarian cancer. Gynecologic Oncology, 54: 227231, 1994. Yamout B, Kyriakides T, Tamim W, Drousiotov A. Myalgia, neuromyopathy and internalized capillaries. A steroid-responsisve syndrome. Acta Neurologica Scandinavica, 91: 294-296, 1995. Deeb L, Yamout B, Shamseddine A, Shabb N, Uthman S. Meningeal Carcinomatosis as the presenting manifestation of gastric adenocarcinoma. Accepted for publication in the American Journal of Gastroenterology, 92: 329-331, 1997. Fayyad M, yamout B, Mroueh S. Alpha Interferon in the Treatment of Subacute Sclerosing. Panencephalitis. Journal of Child Neurology, 12: 486-488, 1997. Nuwayhid I, Yamout B, Azar G. The effects of narghille smoking on pregnancy outcome. The American Journal of Epidemiology, 148: 375-383, 1998. DEXTROSE 30% WATER IV SOLN. DEXTROSE 30% WATER IV SOLN DEXTROSE 60% WATER IV SOLN. TRAVASOL 5% IV SOLUTION TRAVASOL 8.5%-ELECTROLYTES TRAVASOL 8.5% IV SOLUTION POTASSIUM CL 2 MEQ ML VIAL ACETIC ACID 0.25% IRRIG. NOLVADEX 10 MG TABLET DEXTROSE 5%-1 2NS IV SOLN. DEXTROSE 5%-1 2NS IV SOLN. DEXTROSE 5%-1 2NS IV SOLN. DEXTROSE 5%-1 2NS IV SOLN. DEXTROSE 5%-1 2NS IV SOLN. DEXTROSE 5%-1 2NS IV SOLN. DEXTROSE 5%-NS IV SOLUTION DEXTROSE 5%-NS IV SOLUTION DEXTROSE 5%-NS IV SOLUTION DEXTROSE 10%-NS IV SOLUTION RINGERS INJECTION RINGERS INJECTION RINGERS IRRIGATION SOLUTION RINGERS INJECTION SORBITOL 3% UROLOGIC IRRIG D5-1 4NS KCL 10 MEQ L IV SOL D5-1 4NS KCL 20 MEQ L IV SOL D5-1 4NS KCL 20 MEQ L IV SOL D5-1 4NS KCL 30 MEQ L IV SOL D5-1 4NS KCL 40 MEQ L IV SOL D5-1 2NS KCL 10 MEQ L IV SOL D5-1 2NS KCL 20 MEQ L IV SOL D5-1 2NS KCL 20 MEQ L IV SOL D5-1 2NS KCL 30 MEQ L IV SOL D5-1 2NS KCL 40 MEQ L IV SOL D5W KCL 20 MEQ L IV SOLUTION D5W KCL 20 MEQ L IV SOLUTION KCL 20 MEQ NS 500 ML IV SOLN RINGERS INJECTION DEXTROSE 2.5%-1 2 RINGERS DEXTROSE 5%-RINGERS IV SOLN DEXTROSE 5%-RINGERS IV SOLN DEXTROSE 5%-RINGERS IV SOLN DEXTROSE 5%-RINGERS IV SOLN LACTATED RINGERS INJECTION.

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