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4 several years after prilosec was introduced at 20 mg, a 10 mg capsule was finally marketed.
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School children, and have in large part been conducted in summer treatment program or laboratory classroom settings. However, these well-documented gains in daily academic work have not translated into gains in long-term academic achievement MTA Cooperative Group, 1999; Swanson et al., 1995 ; . It is possible that this lack of longterm effects is related to the fact that the school tasks in which children and adolescents typically engage are dramatically different i.e., individual seatwork or teachersupervised worksheets vs. note-taking during lectures, subsequent independent studying, and quizzes and tests ; . Stimulants may not affect the classroom activities in which adolescents engage on a daily basis in the same way that drugs benefit children's daily performance. As was the case 2 decades ago with ADHD children, attempts have been made to evaluate stimulant response in adolescents on laboratory measures or cognitive tasks that are thought to relate to academic performance e.g., Klorman, Brumaghim, Fitzpatrick, & Borgstedt, 1991 stimulants have improved performance on such tasks. However, the correspondence between improvement on these laboratory tasks and actual classroom performance is yet to be tested, and there is no reason to think that it will be better than in childhood. Indeed, there have been very few studies of the relationship between performance on informationprocessing tasks in the laboratory and corresponding measures in the natural environment, and the existing studies have not shown much evidence for such a relationship Kupietz & Richardson, 1978; Lovejoy & Rasmussen, 1990 ; . For example, Pelham and colleagues have obtained only minimal correlations between laboratory and natural measures of attention, particularly when the question is whether drug effects on the laboratory tasks correlate with drug effects in the natural environment Pelham & Milich, 1991; Pelham, Schneider, Evans, & Carlson, 1992 ; . Furthermore, such tasks do not reflect the academic setting in which adolescents with ADHD are typically involved--a classroom in which they are required to attend to a lecture, take notes, study independently, and take quizzes and tests. One small study has examined stimulant effects on such tasks in young adolescents with ADHD. Evans and Pelham 1991 ; reported significant stimulant effects for classroom behavior and direct measures of academic performance in 9 adolescents. Data were collected over a 6-week period in a summer treatment program STP ; during a lecture-format history class. Quiz scores, assignment scores, test scores, behavior observations, and teacher ratings were collected daily in a double-blind, placebo-controlled, randomized stimulant trial. There were significant improvements due to stimulant medication on all of the measures except rule violations and teacher ratings of oppositional and defiant behavior. Although there appeared to be considerable individual differences in response to medication, the small sample size and the design of the trial weekly medication, for example, drug movies.
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Ketoprofen Ketofen ; was originally marketed as a dual inhibitor of cyclooxygenase and 5-lipoxygenase.27 Such activity would broaden the anti-inflammatory potential of the compound, in theory making it superior to other NSAIDs. However, such claims are based on early in vitro data4 and have been challenged with results from experimental models in rats. Ketoprofen had no effect on LTB-4 concentration in such models at doses that produced virtually 100% inhibition of PGE2 and TXB-2 production.28 In two studies involving ketoprofen on exudate eicosanoid concentrations in the horse, the drug significantly reduced PGE2 but not LTB-4 levels. The dose rate used was 2.2 mg kg once or twice daily two doses ; . In another study, synovitis was induced in the mid carpal joint of 12 horses by the injection of carrageenan. Although intravenous administration of ketoprofen significantly reduced PGE2 concentrations in synovial fluid at 6 and 9 h after administration, the LTB-4 levels were unaffected. Joint effusion was reduced at 3 h and lameness was reduced at 3 and 6 h after ketoprofen treatment.29 At clinical doses of 2.2 mg kg d, the drug should not be considered as superior to other NSAIDs based on claims about its ability to inhibit 5-lipoxygenase. In a recent study with experimentally induced synovitis in horses sterile carrageenan ; the analgesic and anti-inflammatory effects of ketoprofen 2.2 and 3.6 mg kg ; and phenylbutazone 4.4 mg kg ; were compared. All NSAID-treated horses had PGE2 compared with saline treated horses. The effect lasted longer with phenylbutazone treated horses than ketoprofen treated horses.30 There were no treatment effects on leukotriene B4 which would supposedly happen if ketoprofen was indeed inhibiting the lipoxygenase pathway ; . Only phenylbutazone treatment reduced lameness, joint temperature, and synovial fluid volume. The conclusion was that phenylbutazone was more effective than ketoprofen in reducing lameness, joint temperature, synovial fluid volume, and synovial fluid PGE2. The results do not support lipoxygenase inhibition by either NSAID and prinivil.
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MILBANK REPRESENTS ASTRAZENECA IN SECOND WAVE PRILOSEC TRIAL: PRILOSEC PATENTS UPHELD AND INFRINGED BY DRUG MANUFACTURERS APOTEX AND IMPAX NEW YORK, June 1, 2007 The Federal district court in Manhattan has found two AstraZeneca formulation patents for Pgilosec both valid and infringed by two manufacturers and distributors of generic omeprazole Prilksec ; . The international law firm Milbank, Tweed, Hadley & McCloy LLP, led by New York-based partner Errol B. Taylor, represented AstraZeneca in this second wave of Prikosec trials. Pril9sec is one of the most widely prescribed medicines in history. Mr. Taylor is long-standing legal advisor to AstraZeneca and led the Milbank trial team that enforced these formulation patents during the second wave of Prilosec litigation and procardia.
Physicians often use an approach called "step therapy" to treat their patients for certain diseases. Under step therapy, select groups of drugs, called "first-line agents, " are used initially. Then, if the first-line agents fail to treat the patient, other groups of drugs, called "second-line agents, " are used. Effective January 1, 2004, preferred drugs in second-line drug classes moved to Tier-3 of our 3-Tier Pharmacy Copayment Program, and the following drugs in second-line drug classes moved to our List of Non-Covered Drugs: Atacand Atacand HCT Avalide Avapro Genotropin Prevacid Prilosec Sporanox capsules only ; Teveten Teveten HC.
If I had AS and it was progressing on objective study, I would opt for early surgery before symptoms appear -- before the myocardium is damaged. RTJ 8-17 EFFECT OF INTRAVENOUS OMEPRAZOLE ON RECURRENT BLEEDING AFTER ENDOSCOPIC TREATMENT OF BLEEDING PEPTIC ULCERS Bleeding recurs in about 20% of patients after endoscopic treatment of bleeding peptic ulcers PU ; . In vivo studies have shown that a high intragastric pH facilitates platelet aggregation and clot formation. Although histamine H2-receptor blockers raise pH to some extent, evidence of their effectiveness in bleeding PUs is conflicting. This study assessed effectiveness of the proton pump inhibitor omeprazole Prilosec ; which maintains intragastric pH at near neutral levels. Does omeprazole, given iv, reduce rate of recurrence of bleeding after endoscopic treatment of bleeding? Conclusion: Omeprazole substantially reduced recurrence rate and promethazine.
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Gested that the decreased Ca2 transient was caused by a reduction of the Ca2 current. Reports of the percent reduction of the Ca2 current produced by metabolic inhibition in ventricular myocytes vary from 17 to 55% 6, 21, ; . We found that the amplitude of the Ca2 current decreased by 23 11% in pacemaker cells, which was small and not statistically significant, making it unlikely that the decrease in the Ca2 transient was entirely due to the inhibition of the Ca2 current. We 15 ; previously showed that in cane toad pacemaker cells, 67% of the Ca2 transient arises from release of Ca2 from the SR. Thus the 65% reduction in SR Ca2 content observed in the present experiments would be expected to reduce the Ca2 transient to 52% 33 67 ; . This is similar to the reduction to 56% that we observed; it seems likely, therefore, that the substantially reduced SR Ca2 content is the main cause of the decreased Ca2 transients. Loading of the SR with Ca2 is a balance between uptake and release. It is known that SR Ca2 -ATPase is inhibited during metabolic inhibition by both acidosis and elevated inorganic phosphate 5, 26 ; . In support of this possibility, we found that the time course of decay of Ca2 transients was significantly slower in the presence of CN . There is also evidence that Ca2 may leak out of the SR through the pump under conditions of metabolic inhibition 24 ; . However, several studies 6, 27 ; in ventricular myocytes have shown that the SR Ca2 content was maintained or increased during metabolic inhibition. Overend et al. 27 ; proposed that the enhanced SR Ca2 content was because the Ca2 spark frequency declined during metabolic inhibition and that this constituted the major leak pathway. Consequently, even though there was a reduction in SR Ca2 uptake, the reduction in Ca2 leak was greater, leading to an increase in SR Ca2 stores. While this may well be true, it is also noteworthy that they inhibited surface membrane Ca2 -ATPase with carboxyeosin in their experiments, which would tend to increase resting [Ca2 ]i and SR Ca2 loading. Whatever the cause of the differences between preparations during metabolic inhibition, it seems clear that in pacemaker cells during brief exposure to CN , the SR Ca2 store is substantially depleted, and this contributes to the reduced Ca2 transients. Possible involvement of cAMP during the metabolic inhibition. In the present study, we found that elevated [cAMP]i could temporarily reverse the effects of CN on the amplitude of the Ca2 transient and on pacemaker activity. One possible explanation is that CN acts through cytochrome P-450 34 ; . Cytochrome P-450 forms a superfamily of proteins that metabolize a range of substrates, including steroids, fatty acids, and drugs for a review, see Ref. 7 ; . Cytochrome P-450 degrades arachidonic acid to epoxyeicosatrienoic acids 28 ; , which stimulate adenylyl cyclase and or inhibit phosphodiesterases, causing increased cAMP production 29, 34 ; . Because oxygen is required for cytochrome P-450-mediated reactions, it has been suggested that failure of cytochrome P-450 activity could.
And if i did not have insurance it would have cost me 27 0 them in the store would have been only 7 00 here in the usai starting to take one nexium in the morning and one prilosec in the evening and propoxyphene.
Women's bodies means to limit women's work in such a way that they cannot escape" Barbieri 1991 ; . Sexual and gender identities and relations are not uniform, and we need to consider ways in which they intersect with other axes of social differentiation. Gender identities vary with the stages of the life cycle, and the meaning of sex and age varies with socioeconomic and ethnic factors in the construction of identities and relations. We must also take into account family structure, economic organization, division of labor, religious beliefs and practices, and other cultural aspects. Gender Relations Gender is a part of all human experience and all social relations, and as such continually influences the value, power and identity of each participant. In general, Latin American societies assign certain political and economic values to men and applaud their roles in public leadership, whereas they assign certain moral values to women and venerate their maternal roles and their functions as transmitters of cultural and religious traditions in the home. These relations are part of social fabrics in which men, in general, have more power for decision-making and action than do women. Nevertheless, is it crucial to remember that this is not a simple dual hierarchy. Each individual's class, ethnic group and generation influence his or her experience within the gender structure. In Bolivia, white adult women in the middle and upper classes have much more power for decision-making and action than do adolescent men who are indigenous peasants. While powerful government, church and economic institutions are dominated by men, it is by an elite group of men. The majority of Bolivian men who are poor, indigenous and poorly educated ; do not in any sense "dominate" the society and enjoy very few privileges, even relative to their wives and sisters. Because we know that gender systems and relationships change, that they have evolved through time and differ across societies, we know that the current situation can change. But since relations of superior power for some and disadvantage for others cross all spheres of life personal, public, private, practical, symbolic - change must be sought in all of these spheres. How do we affect such change? Jeanine Anderson 1997 ; suggests that conflict is inherent in human life. Within a family, conflict between generations is as inevitable as conflict between men and women, due to positions that individuals occupy in the family and society, division of labor and necessary interdependence. Anderson adds, however, that cooperation is also present, as gender systems both channel and regulate relations of conflict and cooperation. Individuals and organizations can make a positive impact on these relations by ensuring that gender conflicts and negotiations are carried out through the democratic processes of dialogue and by refusing to acquiesce to unjust conventions and situations, thus becoming silent accomplices of oppression. Gender and Health Working with sexual and reproductive health from a gender perspective allows us to go beyond a biological focus on women's bodies to a better understanding of men and women's socially construed identities and needs, in order to address the social relations that influence each person's sexual and reproductive health. Services and providers can better respond to user.
| Prilosec for infants dosage44. When assessing the patient's Current Residence M0300 ; , you can: Use interview to determine whether the residence is the patient's or is another type of residence. Tell the type of residence by looking at the dwelling. Call a neighbor to clarify the patient's current residence. Determine whether the residence is a boarding home or rented room, board and care, or assisted living facility by looking around. 45. Mrs. Albers lives alone but is staying with a close friend while she recovers from surgery. In responding to M0300 and M0340: The close friend's home is the current residence M0300--Response 5 ; . The home Mrs. Albers owns is her current residence M0300--Response 1 ; . Mrs. Albers lives alone M0340--Response 1 ; . Mrs. Albers lives with a friend M0340--Response 4 ; . Supportive Assistance 46. The type and quantity of supportive assistance a patient needs: Can be permanent, temporary or occasional. Requires evaluation of the patient's current and anticipated needs. Will be determined by a complete assessment of health status and abilities. Is constant from one assessment point to another. 47. The OASIS items for Supportive Assistance M0350, M0360 ; report: Anyone who helps, including agency staff. Only primary caregivers who are sons or daughters. Those who provide assistance and those who take lead responsibility. Anyone who is paid to provide help. 48. Once it is determined that the patient has a single primary caregiver: Skip to OASIS items for reporting sensory status. Report how often the primary caregiver assists the patient. Report what types of assistance the primary caregiver provides. Address all interview questions only to that person. 49. When assessing Primary Caregiver Assistance M0360, M0370, M0380 ; , consider that: A patient may be hesitant to acknowledge that assistance is needed. You will need to confirm what the patient tells you. The patient has a clear sense of who takes lead responsibility. No one person may take lead responsibility and proventil.
Partnership returns which are recorded in Equity income from affiliates. Such returns include a priority return provided for in the Partnership Agreement, variable returns based, in part, upon sales of certain former Astra USA, Inc. products, and a preferential return representing Merck's share of undistributed AZLP GAAP earnings. These returns aggregated $833.5 million, $646.5 million and $391.5 million in 2005, 2004 and 2003, respectively. The 2003 results reflect a lower preferential return, primarily resulting from the impact of generic competition for Prilosec. The AstraZeneca merger triggers a partial redemption of Merck's limited partnership interest in 2008. Upon this redemption, AZLP will distribute to KBI an amount based primarily on a multiple of Merck's average annual variable returns derived from sales of the former Astra USA, Inc. products for the three years prior to the redemption the Limited Partner Share of Agreed Value ; . In conjunction with the 1998 restructuring, for a payment of $443.0 million, which was deferred, Astra purchased an option the Asset Option ; to buy Merck's interest in the KBI products, excluding the gastrointestinal medicines Nexium and Prilosec. The Asset Option is exercisable in 2010 at an exercise price equal to the net present value as of March 31, 2008 of projected future pretax revenue to be received by the Company from the KBI products the Appraised Value ; . Merck also has the right to require Astra to purchase such interest in 2008 at the Appraised Value. In addition, the Company granted Astra an option to buy Merck's common stock interest in KBI, exercisable two years after Astra's purchase of Merck's interest in the KBI products. The exercise of this option by Astra is also provided for in the year 2017 or if combined annual sales of the two products fall below a minimum amount provided, in each case, only so long as either the Merck option in 2008 or AstraZeneca's option in 2010 has been exercised. The exercise price is based on the net present value of estimated future net sales of Nexium and Prilosec as determined at the time of exercise. The 1999 AstraZeneca merger constituted a Trigger Event under the KBI restructuring agreements. As a result of the merger, in exchange for Merck's relinquishment of rights to future Astra products with no existing or pending U.S. patents at the time of the merger, Astra paid $967.4 million the Advance Payment ; , which is subject to a true-up calculation in 2008 that may require repayment of all or a portion of this amount. The True-Up Amount is directly dependent on the fair market value in 2008 of the Astra product rights retained by the Company. Accordingly, recognition of this contingent income has been deferred until the realizable amount, if any, is determinable, which is not anticipated prior to 2008. Under the provisions of the KBI restructuring agreements, because a Trigger Event has occurred, the sum of the Limited Partner Share of Agreed Value, the Appraised Value and the True-Up Amount is guaranteed to be a minimum of $4.7 billion. Distribution of the Limited Partner Share of Agreed Value and payment of the True-Up Amount will occur in 2008. AstraZeneca's purchase of Merck's interest in the KBI products is contingent upon the exercise of either Merck's option in 2008 or AstraZeneca's option in 2010 and, therefore, payment of the Appraised Value may or may not occur.
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| Drug Name PREVACID I.V. PREVACID NAPRAPAC PREVACID SOLUTAB PREVACID CAPSULES PREVACID PACKETS PREVPAC PRILOSEC PROTONIX ZEGERID CAPSULES ZEGERID PACKETS Genitourinary Agents 5 Alpha-reductase Inhibitors AVODART finasteride PROSCAR Alpha1-adrenergic Blocking Agents CARDURA XL doxazosin mesylate FLOMAX terazosin hcl UROXATRAL Antispasmodics, Urinary DETROL LA DETROL DITROPAN XL ENABLEX flavoxate hcl oxybutynin chloride er oxybutynin chloride syrup oxybutynin chloride tablets OXYTROL SANCTURA VESICARE Genitourinary Agents ELMIRON THIOLA Impotence Agents * LEVITRA * Phosphate Binders FOSRENOL PHOSLO CMS Approval Date: 06 2007 Material ID: H2931002 2931006 2961002 2961011.
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These two clinical studies demonstrated that pfilosec otc was effective in increasing the proportion of patients with no heartburn over 24 hours and that the effectiveness of prilosec otc increases from day 1 to day 1 before using prilosec otc or any medicine, fda advises consumers to read the package label for complete information about the products uses, warnings, and directions and ranitidine.
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Split-up? "This is the question that haunts us, " Analysts are speculating year after year, when Akzo Nobel is going to split-up its hybrid portfolio. Analysts believe its valuation would improve if it spun off its fast-growing pharmaceuticals business. But is it wise to split-up? The group's pharmaceutical operation can be seen as an insulator against the cyclical nature of coatings and chemicals. In March 2001 a split-up was still "highly unlikely": A major break-up is highly unlikely and Mr van Lede stressed that the group has a number of priorities, the first of which is pharmaceuticals. Since many analysts define companies as and relafen and prilosec, because drug testing.
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Lexapro TM escitalopram oxalate ; is marketed by Forest Pharmaceuticals, Inc. Lotensin HCT benazepril HCl hydrochlorothiazide ; is marketed by Novartis Pharmaceuticals Corporation. Lotensin benazepril HCl ; is marketed by Novartis Pharmaceuticals Corporation. Lotronex alosetron HCl ; is marketed by GlaxoSmithKline. Luvox fluvoxamine maleate ; , a discontinued product, was marketed by Solvay Pharmaceuticals, Inc. Mevacor lovastatin ; is marketed by Merck & Co., Inc. Mircette desogestrel ethinyl estradiol ; is marketed by Organon Inc. Monistat 3 miconazole nitrate ; is marketed by McNeil PPC, Inc. Monopril fosinopril sodium ; is marketed by Bristol-Myers Squibb Company. Motrin ibuprofen ; and Motrin Migraine ibuprofen ; are marketed by McNeil Consumer & Specialty Pharmaceuticals. Mycelex -7 clotrimazole ; is marketed by Bayer Corporation. Naprelan naproxin sodium ; is marketed by Elan Biopharmaceuticals. Neulasta TM pegfilgrastim ; is marketed by Amgen. Neurontin gabapentin ; is marketed by Parke-Davis, a division of Pfizer Inc. Nexium esomeprazole magnesium ; is marketed by AstraZeneca LP. Nicorette nicotine ; is marketed by GlaxoSmithKline. Nicotrol nicotine ; is marketed by Pharmacia & Upjohn. Norvasc amlodipine besylate ; is marketed by Pfizer Inc. Orfadin nitisinone ; is marketed by Swedish Orphan International AB. Ortho Tri-Cyclen norgestimate ethinyl estradiol ; is marketed by Ortho-McNeil Pharmaceutical. Ortho-Novum 7 norethindrone ethinyl estradiol ; is marketed by Ortho-McNeil Pharmaceutical. Orudis KT ketoprofen ; is marketed by Whitehall-Robins Healthcare. OxyContin oxycodone HCl ; is marketed by Purdue Pharma L.P. Paxil paroxetine HCl ; is marketed by GlaxoSmithKline. Pegasys peginterferon alfa-2a ; is marketed by Hoffmann-La Roche Inc. Pepcid AC famotidine ; is marketed by Johnson & Johnson-Merck Consumer Pharmaceuticals Co. Plan B levonorgestrel ; is marketed by Women's Capital Corporation. Prevacid lansoprazole ; is marketed by TAP Pharmaceuticals Inc. Preven levonorgestrel ethinyl estradiol ; is marketed by Gyntics Inc. Prilosec omeprazole ; is marketed by AstraZeneca LP. Prinivil lisinopril ; is marketed by Merck & Co., Inc. Prinzide lisinopril hydrochlorothiazide ; is marketed by Merck & Co., Inc. Protonix pantoprazole sodium ; is marketed by Wyeth Pharmaceuticals. Prozac fluoxetine HCl ; is marketed by Eli Lilly and Company. Raptiva TM efalizumab ; is marketed by XOMA Ltd. Rebif interferon beta-1b ; is co-marketed by Serono, Inc., and Pfizer Inc. Remeron mirtazapine ; is marketed by Organon Inc. Remicade infliximab ; is marketed by Centocor, Inc.
Ical science. The collection has a query set and a list of relevant documents for each query. From 50 to 300 documents are judged whether or not relevant to each query. The query consisted of patient information and information request. We used title, abstract, and human-assigned MeSH term fields of documents in the experiments. Since the original OHSUMED is not annotated with tags, we annotated it with tags representing document structures such as " article " and " sentence ", and annotated technical terms with tags such as " disease " and " therapeutic " by longest matching of terms of Unified Medical Language System UMLS ; . In the OHSUMED, relations between technical terms such as events were not annotated unlike the GENIA corpus. The collection consisted of 348, 566 articles, 78, 207, 514 words including tags ; , and 1, 731, 953 sentences. 12 of 106 queries of OHSUMED are converted.
Welcome to the new Infusion Program IP ; column! We will be taking advantage of this publication to routinely provide you with program updates, notification of upcoming events, policy changes, tips for practice improvement and other topics of interest. The IP was formed in January 1998 and is operated by CSU Pharmaceutical Sciences. Originally staffed by two nurse educators, Lynn Chase and Ruth Nicol, the program has recently expanded with the addition of a third educator, Barbara Ferreira and a merger with the I.V. resource nurses Chris Dela Cuesta, Kay Janzen, Carole Leong and Eileen Plunkett ; . Together, these individuals are working to provide parenteral therapy-related clinical, educational and research support to the hospital under the direction of Dr. Peter Jewesson and Frances Legault, PPL, Nursing. Working closely with the IP team is Amy Wai, our Home IV Antibiotic Program clinical pharmacist. To ensure good communication with the balance of the hospital, a 13-member advisory committee was formed in April 1998 with representation from nursing, pharmacy, radiology, vascular surgery, microbiology infection control, infectious diseases and business unit administration. In addition to the well-known and essential clinical services provided by our I.V. resource nurses, a number of specialized functions are also being provided by the IP educators. These include: central venous catheter CVC ; patient teaching via referrals from Vascular Surgery and Radiology CVC device-related complication support; peripherally inserted central catheter PICC ; insertions, teaching.
You have MC + Managed Care health insurance through FirstGuard Health Plan. You may have other health insurance coverage too. This may be from a job, an absent parent, union, or other source. If you have other health insurance besides MC + Managed Care health insurance, that insurance company must pay for most of your health services before FirstGuard Health Plan pays. If your other health insurance covers a service not covered by MC + Managed Care, you will owe your provider what your insurance does not pay. Your health care provider or PCP will take care of this. It is important that you show all your insurance ID cards to your health care provider so that he or she can do this for you. FirstGuard Health Plan and your other health insurance policy have rules about getting health care. You must follow the rules for each policy. For help, call FirstGuard Health Plan at 816-922-7200 or 1-888-828-5698, for example, drug fair.
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