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Generic equivalent available at Tier One copay. If there is a generic equivalent available but you choose to use the brand drug, you will pay the applicable copayment plus the difference in cost between the generic and the brand. PA ; Prior Authorization Required. Please Note: This is not meant to be a complete list of the drugs covered under your plan. Not all dosage forms of the drugs listed above are covered. Brand names are listed for informational reference. Under some circumstances, Preferred drugs may be excluded from your plan for example, oral contraceptives ; . We periodically review our Prescription Drug List. This is the most current list at the time of printing and is subject to change. Some medications may require preauthorization or have quantity limits. Please consult with Pharmacy Help Desk for any questions about your coverage or for more information.
LOMOTIL . Diphenoxylate + Atropine LONITEN . Minoxidil LOPID . Gemfibrozil LOPRESSOR . Metoprolol Tartrate LOPRESSOR HCT . Metoprolol + Hydrochlorothiazide LOPROX . Ciclopirox LORABID . Loracarbef LORCET . Hydrocodone Bitartrate + Acetaminophen LORTAB . Hydrocodone + Acetaminophen LOTEMAX . Loteprednol LOTENSIN . Benazepril LOTENSIN HCT . Benazepril + Hydrochlorothiazide LOTREL . Amlodipine + Benazepril LOTRIMIN AF Clotrimazole LOTRIMIN AF SPRAY POWDER . Mionazole LOTRIMIN ULTRA . Butenafine LOTRISONE . Betamethasone + Clotrimazole LOTRONEX . Alosetron LOVENOX Enoxaparin LOXITANE . Loxapine LOZOL . Indapamide LUCENTISTM . Ranibizumab LUDIOMIL . Maprotiline LUMIGAN . Bimatoprost LUNELLE . Medroxyprogesterone + Estradiol cypionate LUNESTATM . Eszopiclone LUPRON . Leuprolide Acetate LURIDE . Fluoride LUSTRA . Hydroquinone LUTREPULSE . Gonadorelin LUVERIS . Lutropin alfa LUVOX Fluvoxamine Maleate LUXIQ . Betamethasone LYRICATM . Pregabalin LYSODREN . Mitotane MACROBID . Nitrofurantoin Monohydrate, macrocrystals MACRODANTIN . Nitrofurantoin MACUGEN . Pegaptanib MAGNEVIST . Gadopentetate MALARONE . Atovaquone + Proguanil MANDELAMINE . Methenamine MARCAINE . Bupivacaine MARINOL . Dronabinol MARPLAN . Isocarboxazid.
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0% 1. 5-fluorocytosine 15.6uM alverine-citrate 500uM 15. alverine-citrate 500uM 16. alverine-citrate 500uM 17. amphotericin 0.3125uM 18. amphotericin 0.3125uM 19. amphotericin 0.62uM 20. amphotericin 0.62uM 21. atorvastatin 125uM 22. atorvastatin 125uM 23. atorvastatin 62.5uM 24. atorvastatin 62.5uM 25. atorvastatin 62.5uM 26. caspofungin 0.001uM 27. caspofungin 0.001uM 28. caspofungin 0.001uM 29. caspofungin 0.001uM 30. caspofungin 0.0066uM 31. dyclonine 250uM 32. dyclonine 500uM 33. dyclonine 500uM 34. dyclonine 500uM 35. dyclonine 500uM 36. dyclonine 500uM 37. fenpropimorph 1.17uM 38. fenpropimorph 2.34uM 39. fenpropimorph 2.34uM 40. fenpropimorph 4.69uM 41. fenpropimorph 4.69uM 42. fluconazole 32.6uM 43. fluconazole 32.6uM 44. itraconazole 2.2uM 45. itraconazole 4.4uM 46. itraconazole 4.4uM 47. itraconazole 4.4uM 48. itraconazole 4.4uM 49. itraconazole 8.8uM 50. itraconazole 8.8uM 51. itraconazole 8.8uM 52. lovastatin 154.5uM 53. lovastatin 154.5uM 54. lovastatin 154.5uM 55. lovastatin 77.2uM 56. methotrexate 125uM 57. methotrexate 125uM 58. methotrexate 125uM 59. methotrexate 125uM 60. methotrexate 250uM 61. methotrexate 250uM 62. methotrexate 250uM 63. methotrexate 250uM 64. methotrexate 250uM 65. methotrexate 250uM 66. methotrexate 250uM 67. methotrexate 250uM 68. methotrexate 250uM 69. methotrexate 250uM 70. methotrexate 250uM 71. methotrexate 500uM 72. miconazole 0.025uM 73. miconazole 0.025uM 74. miconazole 0.05uM 75. miconazole 0.05uM 76. miconazole 0.05uM 77. miconazole 0.05uM 78. miconazole 0.1uM 79. miconazole 0.1uM 10% 20.
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MATERIALS AND METHODS Isolates. Nine clinical isolates of dermatophytic fungi were selected for this study: T. rubrum strains ATCC 44697, ATCC 44688, and ATCC 44766, Trichophyton mentagrophytes Robin ; Blanchard strains ATCC 18748 and ATCC 44687, Trichophyton tonsurans Malmsten strains ATCC 44689 and ATCC 44690, and Microsporum canis Bodin strains ATCC 44911 and ATCC 44686. These isolates were previously characterized against ketoconazole, miconazole, clotrimazole, and griseofulvin by the freshly prepared microculture susceptibility testing method 3 ; . All isolates were maintained on potato dextrose agar BBL Microbiology Systems, Cockeysville, Md. ; . Antimycotic agents. Stock solutions of griseofulvin Schering Corp., Kenilworth, N.J. ; , miconazole Janssen Research and Development, Inc., New Brunswick, N.J. ; , and clotrimazole Delbay Pharmaceuticals, Inc., Kenilworth, N.J. ; were prepared by dissolving 6 mg of each antimycotic agent in 15 ml 70% ethanol. Dilutions of the stocks were prepared in 50% ethanol so that 10 p.l of each solution would deliver the desired quantity of the drug to the well of a microtiter tray. Ketoconazole Janssen Research and Development.
Patient go to the vaginitis treatment section of the pharmacy and pick up a 15-g tube of miconazole or clotrimazole cream for $7 to $10. Terbinafine cream or spray costs $10 to $13 over the counter, but it reduces the onus of compliance to once-a-day for 1 week. If terbinafine 1% solution is preferred, a 30-mL bottle costs $77. Most of the time, I let the patient make their own choice and monistat.
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In special subacute hepatic studies, oral doses of 125 mg kg and higher in rats were associated with histological changes in the liver which were reversiblewhen the drug was discontinued and nabumetone.
State health departments reported 364 cases in 1997, but it is not a reportable condition in all states.
In recent months we have exhibited at the Primary Care 2001 and NHS Confederation conferences. Visitors to the stand include representatives from Health Authorities, Primary Care Trusts, Primary Care Groups, Dispensing Contractors, General Practitioners, Nurses and Practice Managers. When we exhibit at conferences we are asked about Category D recovery strategy and Electronic Transmission of Prescriptions ETP ; . Information on both of these topics can be found on the PPA websites ppa.nhs & ppa and nizoral.
Be conducted through other media such as regional radio Power FM and 5MU in the Murraylands, 5RM in the Riverland ; and print media through The Stock Journal, Murray Valley Standard and Loxton Times. In addition, there will be extensive promotion through all State media The Advertiser, What's On, Adelaide commercial and ABC radio. With such a catchment area to draw from, this presents our Group with opportunities for good exposure to country people in an area where we have not yet conducted any awareness campaigns. Our site will be situated in the "Future Directions" pavilion, and will be a 3m. undercover site. The site will be located close to other health sites, and local produce sites. The major attraction in this pavilion will be "The Diversity of the Murraylands", which will highlight the many and varied industries and diversification that is happening throughout the Murraylands, along with displays on financial advice, superannuation, communication, education, etc. HOURS of FAIR. Friday gates open at 6.30am for setting up, and will open to the public from 8.30am until 5.00pm. Saturday Gates open at 7.00am and continue to 4.00pm. Gates open to the public from 8.30am. Gates will be locked at 6.00pm. After hours security provided from 5.00pm until 7.00am. All vehicles to be removed from the grounds by 9.00am each day, and there is a special exhibitor's car park. Full catering will be available throughout the Fair by local organisations, with an extensive variety of foods available. Professional caterers will also be in attendance. Also, there will be a full canteen and two bars available. Breakfast will be available on Friday and Saturday mornings, on site.
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NO. Retinas were treated with DPI or L-NAME for at least 45 min before experimentation and for the duration of the experiment. Arachidonic acid metabolites and light-evoked vasomotor responses Previous studies Harder et al., 1998; Zonta et al., 2003; Mulligan and MacVicar, 2004 ; have suggested that arachidonic acid metabolites mediate activity-dependent vasomotor responses in the CNS. To test this hypothesis, we examined whether production of the vasoconstrictor 20-HETE mediates light-evoked vasoconstriction in the retina. In control experiments, light stimulation evoked vasodilation in 40.5% of trials, whereas vasoconstriction was evoked in 28.5% of trials. In the remaining trials, no vasomotor responses were evoked. ; Addition of HET0016, which blocks 20-HETE synthesis by -hydroxylase, decreased the percentage of light-evoked vasoconstrictions to 6.3% and increased vasodilations to 87.5% Fig. 3A ; , indicating that 20-HETE is a mediator of light-evoked vasoconstriction. We also examined whether HET0016 can change light-evoked vasoconstriction to vasodilation in individual vessels. In eight arterioles, which initially displayed light-evoked vasoconstriction in the absence of NOS inhibitors ; , light-evoked vasodilations were observed in all eight after addition of 100 nM HET0016. The role of EETs and prostaglandins in mediating lightevoked vasodilation was also tested. Inhibition of EET synthesis by PPOH reduced the magnitude of light-evoked vasodilations to 3.8 and 23.7% of control in the presence of DPI and L-NAME, respectively Fig. 3B ; . SKF525A and miconazole, two other inhibitors of epoxygenase with different mechanisms of action, similarly reduced the amplitude of light-evoked vasodilations Fig. 3B ; . Inhibition of prostaglandin synthesis by aspirin or indomethacin, in contrast, did not reduce light-evoked vasodilation Fig. 3B ; . We also examined whether PPOH can change light-evoked vasodilation to vasoconstriction in individual vessels. Of 11 arterioles, which initially displayed light-evoked vasodilation in the absence of NOS inhibitors ; , light-evoked vasoconstrictions were observed in seven of them, after inhibition of EET production with 20 M PPOH. The remaining four vessels became unresponsive to light with PPOH. These results indicate that production of EETs, but not prostaglandins, contribute to light-evoked vasodilation in the retina. This conclusion is supported by the finding that superfusion of EET isomers 5, 6-EET, 11, and 17, 18-EET evoked dilation of retinal arterioles, even in the presence of PPOH Fig. 3C ; . Glial-evoked vasomotor responses We also investigated whether glial cell stimulation results in vasomotor responses in the retina. Glial cells were stimulated by increasing intracellular Ca 2 levels. Glial Ca 2 was raised by photolysis of caged Ca 2 , by introduction of IP3 into cells, by photolysis of caged IP3, and by evoked intercellular glial Ca 2 waves. Both Muller cells the principal retinal glial cells ; and astrocytes [which are localized primarily within the nerve fiber layer at the vitreal surface of the retina Newman, 2001a ; ] were tested. Caged Ca 2 stimulation of glia Glial cells were stimulated by flash photolysis of caged Ca 2 after retinal incubation with a membrane-permeant form of the compound. Photolysis of caged Ca 2 resulted in a Ca increase within the stimulated glial cell and, in most trials, initiated a Ca 2 wave that propagated into neighboring glial cells Fig. 4 AC ; movie S4, available at jneurosci as supplemental and orlistat.
ANCOTIL ANCOVENIN h.t. FLUCYTOSINE ANGIOTENSIN-ANTAGONISTS HYPOTENSIVES ACE-INHIBITORS EC-3.4.21.28 ANTICOAGULANTS ANTICOAGULANTS ENZYMES EC-3.4.21.28 DISOPHENOL h.t. h.t. NEMATODE ANTIINFLAMMATORIES NITRIC-OXIDE-SYNTHASE- INHIBITORS ANDROGEN-RECEPTOR androgenization ANDROGENS ANDROGRAPHIS ANDROGRAPHISIDE ANDROGRAPHOLIDE * ANDROID * ANDROJECT * ANDROL ANDROMACO ANDROSIN ISOTHIPENDYL SUCRALFATE MEPROBAMATE androstanazole ANDROSTANE ANDROSTANEDIOL ANDROSTANEDIONE MICONAZOLE h.t. GLYCOGENOSIS HEPATOPATHY CARBOHYDRATE- METAB.DISORDER ANDROSTANOLONE ANDROSTANOLONE-5-BETA ANDROSTANOLONE-BENZOATE androstanolone-enanthate ANDROSTANOLONE-HEPTANOATE androstanolone-nitrate ANDROSTANOLONE-PROPIONATE ANDROSTENEDIOL h.t. SPASMOLYTICS ANDROSTANOLONE h.t. h.t. PROTEIN-METAB.DISORDER PERIPHERAL-NERVE-DISEASE ANTIOXIDANTS P-GLYCOPROTEIN-INHIBITORS ANTIBIOTICS ANDROSTENEDIOL-DIPROPIONATE ANDROSTENEDIONE ANDROSTENONE ANDROSTERONE * ANECTINE ANEMARRHENA ANEMARRHENASAPONIN-I ANEMARRHENASAPONIN-IA h.t. ANTIBIOTICS TESTOSTERONE-UNDECANOATE h.t. FUNGICIDES ANTIBIOTICS CYPROTERONE-ACETATE ANEMIA ANEMIC ANEMONE anemonia-toxin ANENCEPHALY ANEPHRIC ANERGY * ANESTACON * ANESTAN ANESTHESIA-CAUDAL h.t. h.t. KIDNEY IMMUNODEFICIENCY-DISEASE LIDOCAINE HALOTHANE h.t. use BOTANY SEA-ANEMONE-TOXIN-II h.t. h.t. h.t. h.t. use see h.t. h.t. h.t. h.t. h.t. use h.t. use h.t. h.t. h.t. h.t. h.t. h.t. ANTIASTHMATICS STANOZOLOL Appendix B ANDROGENS ANDROGENS ANDROGENS ANABOLICS ANDROGENS ANDROGENS ANDROSTANOLONE- HEPTANOATE ANDROGENS NITROSTANOLONE ANDROGENS ANABOLICS ANDROGENS ANDROGENS ANABOLICS ANDROGENS ANDROGENS ANDROGENS SUXAMETHONIUM CHLORIDE BOTANY ANTIAGGREGANTS ANTIOXIDANTS ANTIAGGREGANTS h.t. h.t. h.t. BOTANY PROTOZOACIDES HEPATOTROPICS METHYLTESTOSTERONE TESTOSTERONE- PHENYLPROPIONATE OXYMETHOLONE h.t. RECEPTOR note Introduced 1985 use VIRILIZATION.
With miconazole, marked hypercholesterolemia and hypertriglyceridemia developed, which subsided after the drug was stopped. Subsequently, amphotericin B was administered, and the infection was eradicated. Prompted by these observations, we did a systematic study to determine the mode by which the drug induced the dyslipoproteinemic condition seen in these two patients and ovral.
Primary: Satisfactory clinical response was reported in 50%, 73.68%, 77.78%, of patients treated with Whitfield's Ointment, tolnaftate, clotrimazole, and miconazole, respectively. Mycological cure was reported in 21.42%, 63.16%, 59.26%, and 77.78% of patients treated with Whitfield's Ointment, tolnaftate, clotrimazole, and miconazole, respectively. Although miconnazole demonstrated the highest clinical and mycological cure rate, there was no statistically significant difference between clotrimazole, miconazole, and tolnaftate treatment groups P 0.05 ; . Clotrimazole, miconazole, and tolnaftate therapies were more efficacious compared to Whitfield's Ointment P 0.05 ; . Secondary: There were no reported adverse reactions.
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FIG. 2. Fat pad weights and plasma leptin levels. A, Perirenal and epididymal fat pad weights and plasma leptin in 1-yr-old LOB T and NT male littermates n 6 ; . B, Perirenal and ovarian fat pad weights and plasma leptin in 1-yr-old LOB T and NT female littermates n 6 ; . * , 0.01; * , P 0.01; * , P 0.001. TABLE 1. Plasma hormones and metabolites in LOB T and NT rats.
Appearances: Petitioner, Stateof Vermont: RobertH. Backus Respondent: did not appear PresidingOfficer: Larry S. Novins DEFAUL T ORDER The Board of Pharmacyheld a hearing on the above matter on September 28, 2005 at the RedstoneBuilding 26 Terrace St. in Montpelier, Vermont. The Respondent not did attend and was not represented counsel. by Findings of Fact 1 Respondent subjectto the regulatory authority of this Board. 3 V.S.A. 129, is 129a, Chapter35 of Title 26 and the Administrative Rules of the Board ofPhamlacy and the Office of ProfessionalRegulation. The Respondent was sentnotice of the Chargesagainsther by certified mail on June 24, 2005 to her last known address. The chargeswere filed on June22, 2005. Ms. Atwood's licensewas summarily suspended that sameday. Ms. Atwood signedthe return receiptindicating receipt of the chargeson June 25, 2005. Ms. Atwood did not file an answerwithin 20 days as required. Notice of the default hearing scheduledfor September 28, 2005 was mailed to that sameaddressby certified mail on September 21, 2005. The letter was receivedand signedfor. The signatureis illegible. The Respondent not answeredthe chargesagainsther. has Upon hearingthe State'spresentation and taking notice of its own file, the Board found the Respondent be in default. The allegationscontained in the State's to specificationof chargesdatedJune 16, 2005 copy attached ; are therefore treatedas the facts on which the Board's orderis based. OPR Rule 3.4, 3 V.S.A. 809 d ; and 3 V.S.A. 814 c and periactin and miconazole, for example, miconqzole nitrate and pregnancy!
Drug Name metronidazole 0.75% gel metronidazole gel 0.75 % metronidazole vaginal gel mupirocin oint silver sulfadiazine silver sulfadiazine silver sulfadiazine silver sulfadiazine sulfacetamide sodium and urea carbamide ; sulfacetamide sodium-sulfur in urea 10-5% emulsion Preferred brands mafenide acetate metronidazole 1% cream mupirocin calcium mupirocin cream Brands bacitracin-polymyxin-neomycin hc erythromycin acne aid ; hexachlorophene metronidazole 1% gel metronidazole vaginal gel neomycin-polymyxin-hc silver nitrate oint silver nitrate solution silver nitrate-potassium nitrate sulfanilamide vaginal DERMATologIcAl AgENTS -- ANTIBIoTIcS Generics benzoyl peroxide-erythromycin gel DERMATologIcAl AgENTS -- ANTIfuNgAlS Generics ciclopirox olamine clotrimazole clotrimazole-betamethasone econazole nitrate ketoconazole miconazlle 3-day combo miconazole vag supp nystatin nystatin nystatin powder nystatin powder nystatin-triamcinolone.
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This work was supported by grants from the American Heart Association AHA 95001370 ; and the National Institutes of Health DK 44628 ; . Dr. Edward W. Inscho is an Established Investigator of the American Heart Association. These studies were performed at Tulane University School of Medicine and at the Medical College of Georgia. The authors wish to thank Dr. John D. Imig for his thoughtful review of the manuscript and Lisette Bourgouis for her excellent secretarial assistance.
I do know that my symptoms resolved after several months on the marshall protocol which relies on specific drug therapies.
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Cinacalet has the potential to interact with other drugs as it is metabolised by multiple enzymes, predominantly CYP3A4 and CYP1A2, and is a potent inhibitor of CYP2D6. See the SPC for possible interactions.5 Patients receiving cinacalcet may need additional monitoring for calcium, phosphate and PTH levels compared to those on standard therapy.6.
Two new sesquiterpene glycosides, 10 S ; -amarantholidol A glucoside 1 ; and 10 R ; -amarantholidol A glucoside 2 ; , together with nine known compounds, amarantholidoside II, amarantholidoside III, 3-caffeoylquinic acid, methyl 3-caffeoylquinic acid, methyl 4-caffeoyl quinic acid, acacetin 7-O--sophoroside, 6-hydroxykaempferol 3glucoside, acid, and sinapyl 4-O--D-glucopyranoside were isolated from the MeOH extract of Saussurea triangulata Compositae ; . Despite a number of studies on the chemical constituents and biological activities of the genus Saussurea, there have been no phytochemical investigations on S. triangulata previously. The isolated compounds were tested for their cytotoxicity against four human cancer lines in vitro using a SRB method. Isolation, structural characterization and bioactivity of the isolated compounds will be discussed in this poster. P-085M: LIGNANS FROM SAURURUS CHINENSIS INHIBITING MELANIN PRODUCTION IN MELANOMA B16 CELLS Chang-Seob Seo1, Won-Hee Lee2, Young-Soo Kim2, Jong-Keun Son1, and Seung-Ho Lee1 1 College of Pharmacy, Yeungnam Universty, Gyongsan, 712-749, Korea. 2College of Pharmacy & Research Center for Bioresource and Health, Chungbuk National Universty, Cheongju 361-763, Korea. The activity-guided fractionation based on melanogenesis inhibition leads to the isolation of five known compounds from the ethyl acetate extract of the roots of Saururus chinensis Saururaceae ; . These were identified as saucerneol B, manassantin B, manassantin A, nectandrin B, and machilin D by spectral evidence. Saucerneol B, manassantin B, manassantin A showed dose-dependent inhibitory effects on 3-isobutyl-1-methylxanthine IBMX ; -induced melanin production in melanoma B-16 cells with IC50 values of 2M, 8nM and 13nM, respectively. Manassantin B, manassantin A exhibited about 10, 000-fold stronger inhibitory effects on melanin production than arbutin, for example, tioconazole vs miconazole.
Biphosphonates and jaw necrosis cancer patients given drugs called bisphosphonates to control hypercalcemia – too much calcium in the blood – or the growth of bone metastases can develop bone death in the jaw the fda warns and mirtazapine.
TABLE 15 Summary details of the economic evaluations Study Bennett et al. and Stinson et al.61 SmithKline Beecham28 Schering-Plough Ltd.62.
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Topical antifungal drugs containing miconazole , clotrimazole , terbinafine , butenafine and tolnaftate , many available without a presciption, are used to clear up the infection.
VIBRAMYCIN . Doxycycline hyclate VIBRA-TABS Doxycycline hyclate VICODIN . Hydrocodone + Acetaminophen VICODIN TUSS . Hydrocodone + Guaifenesin VICOPROFEN . Hydrocodone + Ibuprofen VIDAZATM . Azacitidine VIDEX . Didanosine VIDEX EC Didanosine, enteric-coated VIGAMOX . Moxifloxacin VIOFORM . Clioquinol VIOFORM HYDROCORTISONE . Clioquinol + Hydrocortisone VIOKASE . Amylase + Lipase + Protease VIOXX . Rofecoxib VIRA-A Vidarabine VIRACEPT . Nelfinavir VIRAMUNE . Nevirapine VIRAVAN-S Phenylephrine + Pyrilamine VIRAZOLE . Ribavirin, aerosol VIREAD Tenofovir disoproxil fumarate VIRILON . Methyltestosterone VIRILON IM Testosterone cypionate VIROPTIC . Trifluridine VISICOL . Sodium phosphate VISKEN . Pindolol VISTARIL . Hydroxyzine Pamoate VISTIDE . Cidofovir VITRASERT . Ganciclovir VIVACTIL . Protriptyline VIVAGLOBIN . Immune globulin, subcutaneous VIVELLE . Estradiol, transdermal patch VIVITROLTM . Naltrexone VIVOTIF . Typhoid vaccine, oral VOLMAX . Albuterol, extended-release VOLTAREN . Diclofenac Sodium, enteric-coated VOLTAREN XR Diclofenac Sodium VOSPIRE ER Albuterol, extended-release VUSIONTM . Micoanzole + Zinc oxide VYTONE . Hydrocortisone + Iodoquinol VYTORIN . Ezetimibe + Simvastatin WELCHOL . Colesevelam WELLBUTRIN . Bupropion HCl WELLBUTRIN SR Bupropion HCl, sustained-release WELLBUTRIN XL Bupropion, extended-release WELLCOVORIN . Leucovorin calcium WESTCORT . Hydrocortisone valerate.
The CIRM Interim Policy also requires that, "[g]rantees shall share biomedical materials described in published scientific articles for research purposes in California within 60 days of receipt of a request unless legally precluded."369 This provision is mandatory, but CIRM can provide exceptions to this rule.370 One of the exceptions may include protecting junior researchers. The "unless legally precluded" language appears to allow some materials used perhaps in an industryuniversity collaboration to be withheld by contract. As discussed supra, there is empirical evidence demonstrating that some researchers are having difficult obtaining research materials that are tangible property. While it is unclear whether the cause of that difficulty in accessing materials is because of increased patenting or licensing, this provision should enable researchers to obtain research materials from CIRM grant recipients and mitigate the problems associated to withholding research materials.371.
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