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Medication showed no improvement. Since hay fever, nasal and ocular symptoms are the primary complaints of allergic rhinitis sufferers, we were especially interested in Zicam allergy's effectiveness on these domains. We found that Zicam allergy was very effective in relieving these symptoms p 0.002, p 0.001 and p 0.001 respectively ; . The fact that Zicam Allergy is a homeopathic preparation without the side effects seen with many other OTC medications makes it an attractive alternative for allergy sufferers. Disclosure Statement The author Dr. Sion Nobel was employed by Barron Biotechnologies to conduct this study and serve as independent principal investigator. Barron Biotechnologies was contracted by Gumtech International, the manufacturer of Zicam Allergy Relief to organize a clinical allergy study with the drug. The author was paid a nominal fee based on patient enrollment in the study. Barron Biotechnologies is an independent company which has no vested interest in Gumtech. Barron Biotechnologies received some money but no stock or stock options from Gumtech as payment for the contract. No payments of any kind from Gumtech to Barron Biotechnologies or from Barron Biotechnologies to the author were ever dependent upon any outcomes. References Blaiss M.S. Quality of life in allergic rhinitis. Annals of Allergy, Asthma, and Immunology 1999; 83-449-454. Burge HA, Rogers CA. Outdoor Allergens. Environ Health Perspect. 2000 Aug; 108 Suppl 4: 653-659 ; . Charpin D, Raherison C, Dutau H, Taytard A Epidemiology of respiratory allergies: current data. Rev Mal Respir. 2000 Feb; 17 1 Pt 2 ; 139-58 ; Ellis A.K. Day J.H. and Lundie M.J. Impact on quality of life during an allergen challenge research trial. Annals of Allergy, Asthma and Immunology 1999; 83: 33-39. Fireman P. Therapeutic approaches to allergic rhinitis: treating the child. J Allergy Clin Immunol. 2000 Jun; 105 6 Pt 2 ; S616-21 ; . Guyatt G.H. Feeny D.H. Patrick D.C. Measuring health related quality of life. Annals of Internal Medecine 1993; 118: 622-629. Juniper E.F. Guyatt G.H. Development and testing of a new measure of health status for clinical trials in rhinoconjunctivitis. Clini Exp Allergy 1991; 21: 77-83. Juniper EF, Guyatt GH, Dolovich J, Assessment of quality of life in adolescents with allergic rhinoconjunciitis: development and testing of a questionnaire for clinical trials. J. Allergy and Clinical Immunology 1994 Feb; 93 2 ; : 414-23. Juniper E.F. Guyatt G.H. Griffith L.E., et al. Interpretation of Rhinoconjunctivitis quality of life questionnaire data. J. allergy clin Immunol 1997; 98 4 ; : 843-845. Nathan R. Meltzer E. Selner J. Storms W. Prevelence of allergic rhinitis in the United States. J Allergy clini immunol 1997; 99: s808-814.
Further, I found the testimony of Dr. Iwanow, Plaintiff' long time treater, s more credible as to Plaintiff' work restrictions than the one-shot evaluation of two s semi-retired medical examiners. Also, even Dr. Lyons acknowledged that he would impose restrictions on Plaintiff concerning heavy lifting activities and agreed that the treating doctor should be responsible for the imposition of work restrictions. Defendant' argument in essence is that we should reconsider and reweigh the testimony s below and reach our own conclusions. The follow excerpt is representative of its position on a appeal: Consequently, the Commission is not duty bound to rubber stamp the Magistrate' fact finding upon the discovery of any supporting competent, material and s substantial evidence in the record. Rather, the Commission must evaluate all of the evidence from the "whole record." Having done that, it may even substitute its own findings of fact for those of the Magistrate if it "accords different weight to the quality or quantity of evidence presented." Applying the standard to this case, the Commission should reverse the Magistrate' decision. The competent, material and substantial evidence from the s whole record, evaluated for both quantity and quality, demonstrates the obvious fact that the strain and contusion plaintiff suffered when she slipped and fell in March, 1998, is no longer the cause for whatever low back complaints she might have at the present time. Defendant misstates our powers on appeal. In Mudel v Great Atlantic & Pacific Tea Co, 462 Mich 691 2000 ; , the Michigan Supreme Court revisited the extent of our fact finding powers on appeal. We must briefly take a minute to review what Mudel did and did not do. To begin with, it did not present a new standard of review, or give us the power to disregard the weight given testimony by the magistrate in his or her fact finding.1 What Mudel did do, was return us to the proper statement of our powers on review, originally spelled out in Holden v Ford Motor Co, 439 Mich 257 1992 ; , rejecting the so-called Aany evidence standard promulgated in Goff, for example, parlodel.
Mg123 ; by 90% in healthy Plasma clearance and volume of distribution were reduced by 25% and 20%. respectively.
Guidance can also be found at the front of the BNF under prescription writing. Gill Gookey, Practice Pharmacist YELLOW CARDS What are they? Yellow cards are a voluntary scheme providing a system for early detection of emergency drug safety hazards and routine monitoring for all medicines in clinical use throughout their marketed life. It can result in changes to the prescribing information and occasionally withdrawal of a drug. The Committee of Safety of Medicines CSM ; and the Medicines and Healthcare Products Regulatory Agency MHRA ; monitor yellow card reporting. The bulletin Current Problems in Pharmacovigilance helps keep healthcare professionals up to date with issues highlighted through the reporting system and can be accessed from the CSM website: : medicines.mhra.gov aboutagency re gframework csm csmhome . Data on adverse effects of specific drugs is available from the CSM MHRA. This information can also be accessed via drug information centres. Who Can Use Them? Doctors, dentists, coroners, pharmacists hospital & community ; , nurses, health visitors, midwives, radiographers and optometrists can all report adverse reactions to medications using the yellow card system. It is also currently being piloted for use by patients using a different form, for example, parlodel prescribing information.
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Landmark investigation, called the Seven Countries Study, was launched in the 1950s, when an unexplained epidemic of heart disease was sweeping across the U.S. The study showed that heart attacks were virtually unknown in some regions and the leading cause of death in others--and that the difference was largely a matter of what people ate. Over the next four decades, Keys helped introduce Americans to the glories of the Mediterranean diet. When Keys died in November, researchers around the world paid homage to his life and work. But the biggest tribute is the simple fact that the eating patterns he studied and celebrated remain the exemplar of health eating.
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1st incident: 30 July4 August 1998 2nd incident: 25 August4 September 1998 3rd incident: 519 September 1998 Contamination of potable water supply with Cryptosporidium and Giardia 3.7 million None reported. It is not known why no illnesses were reported despite repeated exposure of the population. Possible explanations are that the organism was a noninfective strain of Cryptosporidium or that the organisms were dead or dying. Methodological issues were also involved. Heavy rains washed animal faeces containing parasites into source water. Inadequate removal of oocysts by coagulation filtration process and periactin.
101. D. A small amount of the umbilical cord The umbilical cord 102. The client is admitted to the unit. A vaginal exam reveals that she is 2em dilated. Which of the following statements would the nurse expect her to make? 103. B. Apply the fetal heart monitor 103. D. Perform an ultrasound exam 108. As the client reaches 8cm dilation, . 108. The FHR baseline is 165-175bpm with variability of 0-2bpm. 108. A. The baby is asleep. 108. C. There is a vagal response. 159. D. Bromocrystine Pardel ; 189. A client is admitted for an MRI. 201. A client with pneumacystis carini pneumonia is receiving trimetrexate. 239. The infant is admitted to the unit with tetrology of falot. 41. B 169. B Which of the following statements would the nurse expect the laboring client during the active phase of labor to make? Apply an internal fetal heart monitor Perform an ultrasound As the client reaches 6cm dilation, . Delete sentence. The baby is sleeping There is a head compression. Bromocriptine Parloddl ; A client is admitted for an CAT scan. A client with pneumacystis carini pneumonia is receiving methotrexate. The infant is admitted to the unit with tetralogy of fallot. A D.
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Connectors, Electrical, Circular Threaded, High Shock, High Density, Shipboard, Class D, General Specification For Comments: All references to ODSs have been removed from this specification. MIL-C-28840, Revision A, Amendment 4, dated 1 April 1993, deletes the ODS reference. The requirement to use 1, 1-Trichloroethane and Trichlorotrifluoroethane for the fluid immersion test See Table X on page 35 ; has been deleted and Superseded by a new table that references method 1016 of MIL-STD-1344 for fluids for the fluid immersion test!
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The antivirus activity of the essential oil from fruit and roots of Heracleum L. species Apiaceae ; was investigated in vivo against influenza Types A and B. The oils, delivered to test animals mice ; by means of oral, intranasal, and inhalation, were distilled in an all-glass Ginsberg's apparatus as described in the USSR Pharmacopoeia ; from autumn-harvested fresh roots and dry, ripe fruits of plants cultivated at the scientific station of the Komarov Botanical Institute of Russian Academy of Science Leningrad district, Priozerskij area ; . Investigations on toxicity indicated that essential oils of Heracleum have a toxicity LD50 at the level of 0.2-0.4 ml. The most effective antiviral activity against influenza in mice was observed when the essential oil was mixed with vegetable oil and given orally as a prophylactic. Results of the study also indicated that the essential oil could be effectively used as a disinfectant for sanitation of lodgings and other materials. Investigations indicated the most active antiviral activity was in oil from H. lehmannianum, H. ponticum, H. aconitifolium. Generally, essential oils from roots had more antiviral activity than oils from fruit. KEYWORDS. Heracleum antasiaticum, H. lehmannianum, H. ponticum, H. aconitifolium, H. stevenii, Apiaceae, hogweed, essential oils, fruit, roots, antiviral activity, toxicity and piroxicam.
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There is no single answer to this question. The treatment of PD is much larger issue than can be discussed here. But the principles of treatment can be described. So far, there is no cure for PD. For most patients, the goal of treatment is to reduce the symptoms of PD to allow the individual to function as normally as possible, and with as few side-effects as possible. Not every patient has the same symptoms, so the treatment needs to be tailored for each individual. In recent years, many new medicines have appeared on the market, and many more are under study. To patients and physicians alike, the array of medications for PD is staggering. The specific choice of therapy depends on the symptoms, degree of disability, personal and occupational responsibilities, and the presence of adverse effects. The most effective medications for PD are drugs that help the dopamine system. Dopamine agonists, like bromocriptine Parlodle ; , pergolide Permax ; , pramipexole Mirapex ; , and ropinirole Requip ; , stimulate dopamine receptors. The most potent medication for PD is levodopa, usually offered in a combined carbidopa-levodopa formulation named Sinemet or as a carbidopa-levodopa-entacapone formulation called Stalevo. Levodopa is an amino acid that is converted into dopamine by an enzyme in the brain. As a class, all dopamine drugs may cause nausea 12 and pletal.
Important: Side-effects of b blockers include cold extremities, and these drugs except perhaps nebivolol ; should be avoided in patients with Raynaud's disease or severe peripheral vascular disease. b Blockers are contraindicated in patients with asthma and in some patients with chronic obstructive pulmonary disease because they cause bronchoconstriction, for example, side effects of parlodel.
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Leading texts on epidemiology and author or co-author of 230 peer-reviewed epidemiologic and statistical articles. See id. 3. In describing their interest in the case, Professors Green and Greenland point out that they are not being compensated for preparing their brief. Their interest is in "having courts understand the appropriate role of epidemiology in lawsuits in which the causal role of an agent is at issue." See id. at 1-2. They "only seek to urge certain scientific and legal principles be employed by this Court in deciding this appeal." Id. 4. Professors Green and Greenland criticize the district court for adopting a standard that either requires epidemiological evidence in toxic tort cases as a threshold matter or, at a minimum, raises the bar for proof of general causation in the absence of epidemiological evidence. They argue that because toxic agents differ, the evidence required to prove causation by various toxic agents must be flexible. See id. at 6-15. a. According to Professors Green and Greenland, an understanding of how the biological mechanisms of an agent operate on the human body is sufficient evidence of medical causation e.g., a bloody nose may be caused by a punch ; . In the case of toxic agents, however, the biological mechanisms by which varying diseases occur are rarely well enough understood to play a substantial role in proof of causation. See id. at 6-7. b. Professors Green and Greenland recognize that where a substantial body of epidemiological evidence exists, it is often the best evidence of general causation e.g., Benedictin, breast implant, asbestos and DES litigation ; . See id. at 7-9. Nevertheless, they also recognize potentially enormous impediments in the development of epidemiological evidence, such as the rarity of certain conditions or diseases, the ethical issues that can arise in exposing subjects to potentially toxic agents, and the time and expense required to conduct a valid epidemiological study. See id. at 5, 10-11. c. Accordingly, they contend that where epidemiological evidence is understandably absent, courts should consider other evidence of causation without skepticism based upon the absence of epidemiological evidence. See id. at 14-15. 5. Professors Green and Greenland next argue that because epidemiological evidence is understandably absent in the case of Parlodel, courts should consider other evidence of causation, including case reports, dechallenge rechallenge tests, biological mechanism evidence, chemistry and animal toxicology studies. See id. at 15-21. a. Professors Green and Greenland acknowledge the limited probity of animal toxicology studies where a substantial body of epidemiology exists. They argue, however, that because of the absence of epidemiological evidence, the district court should have more carefully assessed the probative value of the bromocriptine animal studies, rather than summarily dismissing them on the basis of case law from the Benedictin and breast implant litigation, where substantial epidemiological evidence existed. See id. at 16-18 and premphase.
Brand Name Generic Name ENDACOF-DM ENDACOF-HC ENDACOF-PD HISTACOL BD MYPHETANE DX PEDIAHIST DM PSE BPM HD PSE BROM ROBITUSSIN UNI-HIST DM VISVEX HC BRIMONIDINE TARTRATE BROMOCRIPTINE MESYLATE PARLODEL ACCUHIST BIDHIST-D BPM PSEUDO BROMAXEFED RF BROMFENEX BROMFENEX-PD BROMHIST-NR CARDEC LODRANE LOHIST-PD PSEUBROM RESPAHIST ULTRABROM ULTRABROM PD UNI-HIST BIDHIST BPM CODIMAL-A LODRANE BROMPHENIRAMINE TANNATE BROVEX CT BUMETANIDE BUMETANIDE BUMETANIDE BUMEX BUMEX BUPIVACAINE HCL MARCAINE SENSORCAINE BUPIVACAINE HCL BUPIVACAINE HCL MARCAINE MARCAINE SENSORCAINE SENSORCAINE BUPROPION HCL BUPROPION HCL BUPROPION HCL BUPROPION HCL BUPROPION HCL WELLBUTRIN WELLBUTRIN WELLBUTRIN SR WELLBUTRIN SR WELLBUTRIN SR BUSPAR BUSPAR BUSPAR BUSPAR Generic Description BPM D-METHORPHAN HB P-EPD HCL BPM HYDROCODONE P-EPHED HCL BPM D-METHORPHAN HB P-EPD HCL BPM D-METHORPHAN HB P-EPD HCL BPM D-METHORPHAN HB P-EPD HCL BPM D-METHORPHAN HB P-EPD HCL BPM HYDROCODONE P-EPHED HCL BPM D-METHORPHAN HB P-EPD HCL BPM D-METHORPHAN HB P-EPD HCL BPM D-METHORPHAN HB P-EPD HCL BPM HYDROCODONE P-EPHED HCL BRIMONIDINE TARTRATE BROMOCRIPTINE MESYLATE BROMOCRIPTINE MESYLATE BROMPHENIRAMIN P-EPHED HCL BROMPHENIRAMIN P-EPHED HCL BROMPHENIRAMIN P-EPHED HCL BROMPHENIRAMIN P-EPHED HCL BROMPHENIRAMIN P-EPHED HCL BROMPHENIRAMIN P-EPHED HCL BROMPHENIRAMIN P-EPHED HCL BROMPHENIRAMIN P-EPHED HCL BROMPHENIRAMIN P-EPHED HCL BROMPHENIRAMIN P-EPHED HCL BROMPHENIRAMIN P-EPHED HCL BROMPHENIRAMIN P-EPHED HCL BROMPHENIRAMIN P-EPHED HCL BROMPHENIRAMIN P-EPHED HCL BROMPHENIRAMIN P-EPHED HCL BROMPHENIRAMINE MALEATE BROMPHENIRAMINE MALEATE BROMPHENIRAMINE MALEATE BROMPHENIRAMINE MALEATE BROMPHENIRAMINE TANNATE BROMPHENIRAMINE TANNATE BUMETANIDE BUMETANIDE BUMETANIDE BUMETANIDE BUMETANIDE BUPIVACAINE HCL BUPIVACAINE HCL BUPIVACAINE HCL BUPIVACAINE HCL PF BUPIVACAINE HCL PF BUPIVACAINE HCL PF BUPIVACAINE HCL PF BUPIVACAINE HCL PF BUPIVACAINE HCL PF BUPROPION HCL BUPROPION HCL BUPROPION HCL BUPROPION HCL BUPROPION HCL BUPROPION HCL BUPROPION HCL BUPROPION HCL BUPROPION HCL BUPROPION HCL BUSPIRONE HCL BUSPIRONE HCL BUSPIRONE HCL BUSPIRONE HCL Strength 30-60-4 5 30-1.7-2 ML 6MG 12MG ML 1MG 2MG 1MG ML 2.5MG ML 2.5MG ML 5MG ML 7.5MG ML 5MG ML 7.5MG ML 5MG ML 7.5MG ML 75MG 100MG Form Code SYRUP SOLUTION DROPS DROPS SYRUP DROPS SOLUTION SYRUP SYRUP DROPS SYRUP DROPS TABLET TABLET DROPS TAB.SR 12H TAB.SR 12H SYRUP CAPSULE SA CAPSULE SA DROPS SYRUP TAB.SR 12H DROPS CAPSULE SA CAPSULE SA CAPSULE SA CAPSULE SA DROPS TAB.SR 12H TAB.SR 12H VIAL TAB.SR 12H TAB CHEW TAB CHEW VIAL TABLET TABLET TABLET TABLET VIAL VIAL VIAL VIAL VIAL VIAL VIAL VIAL VIAL TABLET TABLET TABLET SA TABLET SA TABLET SA TABLET TABLET TABLET SA TABLET SA TABLET SA TABLET TABLET TABLET TABLET.
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Combining Science and Technology to Create Advanced Drug Delivery Systems OUR MISSION STATEMENT: Modern drug delivery research and development is a truly multidisciplinary approach and must combine all relevant scientific, technical, medical and regulatory aspects required for the design, preparation, testing, manufacturing and registration of drug delivery systems and their components. It is the mission of the APV Drug Delivery Working Group to foster and promote all aspects of research and development required to transform drug molecules into safe, applicable and acceptable drug delivery systems, which provide therapeutic benefit, convenience to the patient and improve patient compliance and proscar.
Pril, the teratogenic risk appears to be similar for the entire drug class. These ACE inhibitors have been associated with severely underdeveloped calvarial bone, renal failure, oligohydramnios, anuria, renal dysgenesis, pulmonary hypoplasia, IUGR, fetal death, neonatal renal failure, and neonatal death 4246 ; . Fetal risks with ACE inhibitors depend on timing and dose. For example, the use of ACE inhibitors during the first trimester before renal tubular function begins ; has not been associated with an increase in birth defects 47, 48.
| We have identified a highly homologous cathepsin Z-like cysteine protease of Onchocerca volvulus in Caenorhabditis elegans 82% ; that we named Ce-cpz-1. we used C. elegans as the model system for studying the function of both enzymes. In O. volvulus, cathepsin Z appeared to be essential during the molting of L3, however, its function in the other stages of the parasitic nematode was difficult to study. Disruption of cpz-1 function by RNA interference indicated an important role for cpz-1 during molting of L2, L3 and L4. Stage-specific C. elegans worms that were soaked in dsRNA or fed on Ce-cpz-1 dsRNA developed various molting defects, including incomplete shedding of the old cuticle, formation of a mouth plug in the molting worms, and incomplete expulsion of the pharynx during the L4 adult molt. The role of CPZ1 during molting is supported by the spatial pattern of cpz-1 expression in transgenic worms; various hypodermal cells in all developmental stages and in the pharynx of adult worms, as well as the cyclic expression of the transcript during the molting periods. Moreover, the native CPZ-1 protein was present in the cuticular region of larval and adult C. elegans stages and along the length of the pharynx of adult worms. Notably, localization of the native protein by immunoelectron microscopy have clearly showed that the enzyme is present specifically in the area between the new and the old cuticles of molting worms that is degraded prior to ecdysis and shedding of the old cuticle. Similar localization of the related O. volvulus CPZ protein in molting L3 suggests that both enzymes are functional homologues and may have a direct role in degrading cuticular proteins. Alternatively, they may be involved indirectly in the processing and or activation of other enzymes or peptide hormones that are essential during the molting process in both nematodes and provera and parlodel, for example, drug information.
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The state PIRGs support the following common sense solutions to the problem of overpriced prescription drugs. Increase the Availability of Generic Drugs. Lower-cost generic drugs could save Medicare, Medicaid and consumers billions of dollars. The state PIRGs support increasing the Food and Drug Administration's budget devoted to approving generic drug applications in order to ease the substantial backlog. We also support closing loopholes that allow.
AWARD Silver URL : nkdep.nih.gov familyreunion ENTRY TITLE NKDEP's Family Reunion Initiative CLASS Health Promotion Disease & Injury Prevention Information CATEGORY Web Site DIVISION Government AUDIENCE All Adults 21 + years, for example, parlodel drug.
Association of international pharmaceutical manufacturers, "counterfeit medicines rise to 12 percent of total russian market, " press release, association of international pharmaceutical manufacturers, april 25, 2002 and periactin.
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Surgical approaches56 Over the years, surgery for phaeochromocytoma has evolved from the classical midline open approach to the retroperitoneal approach to laparoscopic surgery and even partial adrenalectomy. The obvious benefit of the open approach is better access permitting exploration for other tumours in cases of extra-adrenal tumours and metastases. Mortality is usually low in most cases. In a large surgical series, peri-operative mortality and morbidity rates for phaeochromocytomas were 24% and 24% respectively.57 The incidence of splenic complications was particularly high at 8%. Independent risk factors for complications are high pre-operative systolic blood pressure, high urinary metanephrine excretion and number of re-operations. Immediate post-operative period Post-operative monitoring for hypoglycemia is important. High levels of circulating catecholamines increase glycogenolysis and gluconeogenesis via its 1 and 2 adrenergic effects and lipolysis via its 3 effect. This leads to pre-operative hyperglycaemia in 60% patients.33 However, removal of the tumour results in a decrease in catecholamine levels and may cause hypoglycaemia from rebound hyperinsulinaemia. The use of blockers may further worsen the situation by blocking the adrenergic symptoms of hypoglycaemia. Approximately 50% patients remain hypertensive postoperatively due to elevated catecholamine stores in adrenergic nerve endings. Most instances of hypertension usually resolve within a week.48 Persistence of immediate post-operative hypertension can be due to pain from insufficient analgesia, the presence of a residual tumour from inadequate resection and drugs which include antiemetics like droperidol, which block 2 receptors and metoclopropamide, a dopamine and 5-hydroxytryptamine receptor antagonist. The other post-operative complication is hypotension, which can be due to intravascular volume depletion from inadequate fluid replacement, hypovolaemia from intraabdominal bleeding, residual effects of pre-operative adrenergic blockade and alteration of vascular compliance.33, 58.
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Patients Using Drug, % 95% CI ; 12.5 11.2-13.8 ; 0.5 0.3-0.8 ; 0.4 0.2-0.7 ; . 1.2 0.8-1.7.
Are taking the medication, or is the drug altering a fundamental abnormality long-term and providing some sustained protective effect. A washout period was included in the study design and the results will soon be announced. Because altering the progression of hyperglycemia prevents microvascular complications and possibly even macrovascular disease, a safe approach that delays microvascular complications is worthwhile, whether we actually prevent diabetes or not.
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