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Referenz 224 Neurologie, 11. Auflage ; Del Brutto OH, Santiban~ez R, Noboa CA, Aguirre R, Diaz E, Alarcon TA. Epilepsy due to neurocysticercosis: analysis of 203 patients. Neurology 42: 389-392, 1992 Neurologic Service, Hospital Regional del Instituto Ecuatoriano de Seguridad Social, Guayaquil, Ecuador. We reviewed clinical, EEG, and CT findings of 203 patients with epilepsy due to neurocysticercosis. Seizures were generalized in 121 patients and partial in 82. Thirty-two patients had focal signs and eight had papilledema. Eighty-one had generalized and 16 had focal EEG abnormalities. CT showed parenchymal brain calcifications in 53 patients and cysts in 150. There was an increased rate of focal signs in patients with single cysts as compared with patients with multiple cysts, and focal EEG abnormalities were present only in patients with single cysts. Fifty patients were lost to follow-up. The remaining 153 patients were followed for 28 + - 6 months; of these, 31 had calcifications and 122 had cysts. Anticonvulsants were started after the first visit in every patient. The 31 patients with calcifications remained free of seizures. Ninety-five of the 122 patients with cysts were also treated with anticysticercal drugs; of these, 79 83% ; had control of seizures. In contrast, only seven 26% ; of 27 patients who did not receive anticysticercal drugs had control of seizures, indicating a strong correlation between the use of anticysticercal drugs and seizure control. Finally, of the 21 patients in whom anticonvulsants were withdrawn, 16 had relapses and indapamide.
And, remember the upheaval and confusion during the implementation of Medicare Part D? DPW needs to be very well prepared for an influx of calls, complaints, letters and appeals from the million members and their families who will be affected by the Carve Out.
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Thirteen experiments were performed with eight couples three couples performed two experiments each ; and three single women. The table shows age, weight height index, parity, type of contraception, female orgasm yes no ; , and the depth of penetration partial or complete ; . No women reported having a "g-spot" or producing female ejaculation during orgasm. On two Saturdays in 1991 experiments 1 and 2 ; the first couple succeeded with complete penetration that lasted sufficiently long for the images to be taken. The and isoflavone.
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Move increases their profits. Many drugs make the switch to over-thecounter availability because of a "generic defense, " said Steve Francesco, president of Francesco International. When a drug patent is about to expire, the company submits a switch request in the hopes that brand recognition and loyalty cultivated among prescription customers will transfer to the over-the-counter market. The WaxmanHatch Act of 1984 added another incentive: granting 3 additional years of market exclusivity to drug makers if they perform the extra clinical trials required to gain overthe-counter approval. If a drug has proved to be safe and effective when dispensed on a prescription-only basis and the over-thecounter request is for the same indication at the same or a lower dose, the FDA focuses on evidence that patients can use the drug properly without physician guidance. This evidence often comes from "actual-use" studies, which attempt to mimic consumer use of over-the-counter drugs, and label-comprehension studies, to see how well consumers can extract critical information from package labels. "The studies performed to switch a drug often test the consumer more than they test the drug, " wrote Randy P. Juhl, PhD, RPh, dean of the University of Pittsburgh School of Pharmacy in Pennsylvania Clin Ther. 1998; 20 Suppl C: C111-7 ; . He notes that the studies must address four questions: "Can they read the label? Can they understand the label? Do they follow the label? And do they achieve the desired outcome? All four levels of inquiry help to determine whether a consumer can use a product [safely and effectively] and
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How institutions respond to adverse events is vitally important if an organization is to build a culture of safety. With respect to patients and their families, a consensus has emerged that the most appropriate and ethical course is to immediately disclose an adverse event. Doing so is now required by new regulations from the Joint Commission on Accreditation of Healthcare Organizations 49 ; . A report from the Department of Veterans Affairs argued persuasively for a full-disclosure policy and described one of its medical centers that has had moderate liability payments since implementing this approach in 1987 50 ; . The fear, of course, is that increased reporting, especially coupled with disclosure, could lead to skyrocketing malpractice litigation rates in the United States. A no-fault compensation approach for medical injuries 51 ; may alleviate this problem, but the obstacles are substantial. The current system strongly pressures providers to hide accidents rather than to bring them forward as a means to fuel quality improvement. Furthermore, persons who report adverse events may be punished 52 ; . The tone set by administrators is crucial. Although remedial action should be taken, leadership must resist strong pressures to use individual workers as scapegoats, even when a serious error is found. Organizations that yield to these pressures will find it exceptionally difficult to develop a safety-oriented culture. When given the opportunity to respond anonymously, individual providers recognize that error is a serious issue, but they harbor many counterproductive feelings that.
Zinc The most common enzyme in the membrane of the taste bud is alkaline phosphatase, for which zinc is the co-factor. Zinc and other metals ; also affects the conformation of the protein that regulates the passage of tastants through the taste bud pore.A deficiency in zinc has been linked to altered taste in several groups of patients including those with cancer. Drugs that chelate zinc have also been associated with taste disturbance. However, the exact role of zinc in the control of taste is not fully known. Many trials have been conducted in patients undergoing radiotherapy and it is not clear if the data can be applied to patients with taste disturbances due to other causes. Zinc supplements may be helpful in patients with altered taste which remains unresolved by good oral hygiene and is and vasodilan.
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Akaike HA 1974 ; A new look at the statistical model identification. IEEE Trans Automat Control 19: 716 723. Ambre JJ, Connelly TJ and Ruo TI 1991 ; A kinetic model of benzoylecgonine disposition after cocaine administration in humans. J Anal Toxicol 15: 1720. Bedford JA, Borne RF and Wilson MC 1980 ; Comparative behavioral profile of cocaine and norcocaine in rats and monkeys. Pharmacol Biochem Behav 13: 69 75. Benuck M, Lajtha A and Reith MEA 1987 ; Pharmacokinetics of systemically administered cocaine and locomotor stimulation in mice. J Pharmacol Exp Ther 243: 144 149. Booze RM, Lehner AF, Wallace DR, Welch MA and Mactutus CF 1997 ; Dose-response cocaine pharmacokinetics and metabolite profile following intravenous administration and arterial sampling in unanesthetized, freely moving male rate. Neurtoxicol Teratol 19: 715. Chan KKH and Gibaldi M 1990 ; Effects of first-pass metabolism on metabolite mean residence time determination after oral administration of parent drug. Pharm Res 7: 59 63. Cheng H and Jusko WJ 1993 ; Mean residence time of oral drugs undergoing first-pass and linear reversible metabolism. Pharm Res 10: 8 13. Elliott PJ, Rosen GM and Nemeroff CB 1987 ; A comparison of cocaine and its metabolite nococaine: effects on locomotor activity. Pharmacol Biochem Behav 26: 573575. Epstein DH, Silverman K, Henningfield JE and Preston KL 1999 ; Low-dose oral cocaine in humans: acquisition of discrimination and time-course of effects. Behav Pharmacol 10: 531 542. Hawks RL, Kopin IJ, Colburn RW and Thoa NB 1974 ; Norcocaine: a pharmacologically active metabolite of cocaine found in brain. Life Sci 15: 2189 2195. Inaba T 1989 ; Cocaine: pharmacokinetics and biotransformation in man. Can J Physiol Pharmacol 67: 1154 1157. Inaba T, Stewart DJ and Kalow W 1978 ; Metabolism of cocaine in man. Clin Pharmacol Ther 23: 547552. Jatlow PI 1987 ; Drug of abuse profile: cocaine. Clin Chem 33: B66 B71. Jeffcoat AR, Perez-Reyes M, Hill JM, Sadler BM and Cook CE 1989 ; Cocaine disposition in humans after intravenous injection, nasal insufflation snorting ; , or smoking. Drug Metab Dispos 17: 153159. Johanson C and Fischman MW 1989 ; The pharmacology of cocaine related to its abuse. Pharmacol Rev 41: 352. Jufer RA, Walsh S and Cone EJ 1998 ; Cocaine and metabolite concentrations in plasma during repeated oral administration: development of a human laboratory model of chronic cocaine use. J Anal Toxicol 22: 435 444. Lau CE, Ma F and Falk JL 1990 ; Simultaneous determination of cocaine and its metabolites with caffeine in rat serum microsamples by high performance liquid chromatography. J Chromatogr 532: 95103. Lau CE, Ma F, Foster DM and Falk JL 1999 ; Pharmacokinetic-pharmacodynamic modeling of and ketorolac.
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1E4 TRANSPORT OF AIR POLLUTANTS TO TONTO NATIONAL MONUMENT: A 13 YEAR HISTORICAL STUDY OF AIR TRAJECTORY AND AEROSOL CLUSTER ANALYSIS. CHARITY COURY, Ann Dillner, Department of Chemical and Materials Engineering and Department of Civil and Environmental Engineering, Arizona State University, Tempe, AZ The visibility in Class I areas is protected by the Clean Air Act, Sec. 169A. a ; 1 ; , which requires the remedy of existing visibility impairment and the prevention of any future visibility impairment in these federally mandated areas. The visibility degradation is caused by light scattered and absorbed by aerosol particles. Class I areas adjacent to large urban areas are particularly difficult to protect due to transport of primary aerosols from these urban areas and secondary aerosols formed during transport. Therefore characterization of the aerosol, its source regions and its contribution to light extinction in Class I areas provides information that can assist regulators in reducing visibility degradation from particulate matter. The Interagency Monitoring of Protected Visual Environments IMPROVE ; network established aerosol monitoring sites within many Class I areas beginning in the late 1980's in order to establish current visibility conditions, track changes in the visibility and determine mechanisms causing visibility degradation. The Superstition Wilderness, a Federal Class I area located approximately 60 miles east of the Phoenix, AZ metro area, is effected by dominant air flow during much of the year from Phoenix. In order to better understand the sources of visibility degradation and the historical trends in air transport and aerosol data at Tonto National Monument a site in the Superstition Wilderness ; , air trajectories following the path of air parcels arriving in Tonto National Monument TNM ; have been examined and compared to trends in aerosol data available from IMPROVE network ; at the TNM site for the past 11 years. 24 -hour back trajectories were obtained using NOAA's HYSPLIT model for everyday that aerosol data is available from the IMPROVE network at the TNM site. Trajectories that exhibited a large spatial variance over the 24 trajectories computed for each day were not considered in the analysis. The 24 hour trajectories that displayed consistent air parcel paths for the entire day were averaged to give a single representative trajectory for that day. These daily averaged trajectories were clustered by spatial similarities using Ward's method, where resulting statistical clusters represent similar meteorological patterns. The cluster-averaged historical aerosol data was analyzed according to air parcel source region urban area, power plant, etc. ; . This method gives aggregate pollution data based on similarities in meteorological conditions at the TNM site. The results of this study are presented and show five major meteorological clusters with different pollution source influences. The chemical composition of air traveling over different source areas in and around Arizona and visibility degradation effects in Tonto National Monument will be discussed.
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He quinolones are an important class of broadspectrum antimicrobials in common use today. Multiple quinolones are currently available in the United States Table 1 ; with broader spectrums and longer half-lives than older quinolones, such as nalidixic acid Fig 1A ; . Originally, quinolones as a class were shown to have good activity against Gram-negative rods and were useful in urinary tract infections. Recently, there has been an explosion in the development of these antimicrobials, and they are now used for a variety of infections, including cutaneous diseases. In this review, we will focus on the peculiarities of the quinolones in respect to cutaneous infections and side effects, as well as their use and side effects in other organ systems.
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Excise duty on all anti-HIV drugs. In an attempt to make prices even more affordable, Aurobindo Pharma successfully appealed to the concerned authorities to waive the sales tax at the central and state levels 7 8. Marketing and distribution Citadel's strategy has been to offer discounted not donated ; prices to capture volume sales, in bulk to NGOs, and in some states through retail. Imunus pioneered the concept of service to patient and made efforts to trim distribution channels by reaching out to NGOs and positive people's networks and self help groups SHGs ; directly. It was the first generic manufacturer in India to target the informal sector and this has helped it gain a large customer base. Imunus is the only division among the generic HIV medicine manufacturers to solely deal with HIV products. Its HIV portfolio also includes two drugs for opportunistic infections. Overall, the margins are very low compared to other divisions. While the company has not disclosed the exact financial breakup, it has hinted that some amount of subsidisation from other business areas is required. In West Bengal, where the purchasing power of patients is especially low compared to other states, partnerships with NGO networks has been essential to gain market share. The TANSACS Pharmacy, attached to the Tamil Nadu State AIDS Control Society, offers company products at special discounts to patients, which are not available elsewhere in the state. Cipla has offered discounts on two of its products at the pharmacy, while both Citadel and Ranbaxy have given discounts on a range of products. This distribution model has assured Citadel a steady monthly income and discounts at the pharmacy have been made possible by eliminating the middlemen. Citadel's monthly sales figures unavailable ; have been rising steadily in the process see annex 5 for drug prices at TANSACS Pharmacy ; . TANSACS sales increased from Rs 80, 000 USD$1, 739 ; in December 2003 launched on December 15 ; , to Rs 3.5 lakh USD$7611 ; in March 2004. The average sales figure per day is approximately Rs 15, 0007 9 $326 ; . Citadel's income from TANSACS Pharmacy is around Rs 2 lakh USD$4355 ; a month. Diagnostics Citadel has been working for a year with four doctors in two cities Bangalore and Coimbatore with about 25 patients. Citadel reimburses the cost of the diagnostic test twice a year ; to patients if they take Citadel medicines for six months, from the second diagnostic test onwards. The arrangement appears to be working well. We have not explored potential treatment distorting effects, nor did we assess the consistency of this against local market regulations but this is clearly an important consideration, because atenolol.
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Tuberculin skin test 363 384 had Tuberculin skin test Mantoux ; administered and read 76 363 21% ; had a Mantoux reaction 15mm or greater Not stated Uptake of screening not reported Study examined numerous health outcomes, including Mantoux test and potential clinical symptoms of tuberculosis. No follow-up reported of those individuals with potential clinical symptoms of tuberculosis Study provided very little data on tuberculosis 68.
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Conidial fungi, some of which grow and sporulate in situ and contribute to the breakdown of organic debris. Other species are transients sporulating onf\xposed substrates and passively dispersed in air currents. pense clouds of conidia may be transported over long distances, some of which colonize new subtrates on the surface of the soil. A few species have supplemenrted passive air current dissemination with mechanisms of forcible discharge of their conidia Fig. 21A to C ; . Webster 429 ; has recorded projections of the large, pigmented conidia of Nigrospora sphaerica Fig. 21A ; over vertical and horizontal distances of 2 and 6.7 cm, respectively. A narrow channel provides for cytoplasmic continuity between the ampulliform conidiogenous cell ac ; and young, developing conidium. A supporting collar sc ; holds the conidium in position at the apex of the fertile cell. The latter is thick walled and apparently establishes an internal hydrostatic pressure as the conidium reaches maturity. When the fungus is subjected to desiccating conditions, the pressure within the conidiogenous cell is released by expulsion of its cytoplasmic contents through the narrow channel. This results in separation of the conidium from the supporting collar and its propulsion into the air 429, 432 ; . The.
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1. American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition. Washington, DC: American Psychiatric Association; 1994. 2. Schneier FR, Heckelman LR, Garfinkel R, Campeas R, Fallon BA, Gitow A, Street L, DelBene D, Liebowitz MR. Functional impairment in social phobia. J Clin Psychiatry. 1994; 55: 322-331. Stein MB, Torgrud LJ, Walker JR. Social phobia symptoms, subtypes, and severity. Arch Gen Psychiatry. 2000; 57: 1046-1052. Kessler RC, Stein MB, Berglund P. Social phobia subtypes in the National Comorbidity Survey. J Psychiatry. 1998; 155: 613-619. Lang AJ, Stein MB. Social phobia: prevalence and diagnostic threshold. J Clin Psychiatry. 2001; 62 suppl 1 ; : 5-10. 6. Kessler RC, McGonagle KA, Zhao S, Nelson CB, Hughes M, Eshleman S, Wittchen HU, Kendler KS. Lifetime and 12-month prevalence of DSM-III-R psychiatric disorders in the United States. Arch Gen Psychiatry. 1994; 51: 8-19. Schneier FR, Hornig CD, Liebowitz MR, Weissman MM. Social phobia: comorbidity and morbidity in an epidemiologic sample. Arch Gen Psychiatry. 1992; 49: 282-288. Weiller E, Bisserbe JC, Boyer P, Lepine JP, Lecrubier Y. Social phobia in general health care: an unrecognized undertreated disabling disorder. Br J Psychiatry. 1996; 168: 169-174. Davidson JR, Hughes DC, George LK, Blazer DG. The boundary of social phobia: exploring the threshold. Arch Gen Psychiatry. 1994; 51: 975-983. Lecrubier Y, Weiller E. Comorbidities in social phobia. Int Clin Psychopharmacol. 1997; 12 suppl 6 ; : S17-S21. 11. Katzelnick DJ, Kobak KA, DeLeire T, Henk JH, Greist JH, Davidson JRT, Schneier FR, Stein MB, Helstad CP. Impact of generalized social anxiety disorder in managed care. J Psychiatry. 2001; 158: 1999-2007. Judd LL. Social phobia: a clinical overview. J Clin Psychiatry. 1994; 55 suppl 6 ; : 5-9. 13. Reich J, Goldenberg I, Vasile R, Goisman R, Keller M. A prospective followalong study of the course of social phobia. Psychiatry Res. 1994; 54: 249-258. Liebowitz MR. Update on the diagnosis and treatment of social anxiety disorder. J Clin Psychiatry. 1999; 60 suppl 18 ; : 22-26. 15. Argyropoulos SV, Bell CJ, Nutt DJ. Brain function in social anxiety disorder. Psychiatr Clin North Am. 2001; 24: 707-722. Knutson B, Wolkowitz OM, Cole SW, Chan T, Moore EA, Johnson RC, Terpestra J, Turner RA, Reus VI. Selective alteration of personality and social behavior by serotonergic intervention. J Psychiatry. 1998; 155: 373-379. Tancer ME, Mailman RB, Stein MB, Mason GA, Carson SW, Golden RN. Neuroendocrine responsivity to monoaminergic system probes in generalized social phobia. Anxiety. 1994-1995; 1: 216-223. Smith GS, Dewey SL, Brodie JD, Logan J, Vitkun SA, Simkowitz P, Schloesser R, Alexoff DA, Hurley A, Cooper T, Volkow ND. Serotonergic modulation of dopamine measured with [11C] raclopride and PET in normal human subjects. J Psychiatry. 1997; 154: 490-496.
Pharmacists should participate in, at a minimum, a self-checking process in reading prescriptions, labeling drug or ingredients and pharmacist-generated labeling ; , and dosage calculations. For highrisk drug products, when possible, all work should be checked by a second individual preferably, another pharmacist ; . Pharmacists must make certain that the following are accurate: drug, labeling, packaging, quantity, dose, and instructions. 8. Pharmacists should dispense medications in ready-toadminister dosage forms whenever possible. The unit dose system is strongly recommended as the preferred method of drug distribution. The need for nurses to manipulate drugs e.g., measure, repackage, and calculate ; prior to their administration should be minimized. 9. Pharmacists should review the use of auxiliary labels and use the labels prudently when it is clear that such use may prevent errors e.g., "shake well, " "for external use only, " and "not for injection" ; . 10. Pharmacists should ensure that medications are delivered to the patient-care area in a timely fashion after receipt of orders, according to hospital policies and procedures. If medication oses are not delivered or if therapy is delayed for any reason pending resolution of a detected problem e.g., allergy or contraindications ; , the pharmacist should notify the nursing staff of the delay and the reason. 11. Pharmacists should observe how medications are actually being used in patient-care areas to ensure that dispensing and storage procedures are followed and to assist nurses in optimizing patient safety. 12. Pharmacy staff should review medications that are returned to the department. Such review processes may reveal system breakdowns or problems that resulted in medication errors e.g., omitted doses and unauthorized drugs ; . 13. When dispensing medications to ambulatory patients e.g., at discharge ; , pharmacists should counsel patients or caregivers and verify that they understand why a medication was prescribed and dispensed, its intended use, any special precautions that might be observed, and other needed information. For inpatients, pharmacists should make their services avail-able to counsel patients, families, or other caregivers when appropriate. 14. Pharmacists should preview and provide advice on the content and design of preprinted medication order forms or sheets if they are used. Amal Jawaheer - Mesnil Pharmacy.
Victims Services Local Policy Board Requirements, revised June 2004. STOP Funding Announcement, 2007. Rights and Services Act RASA ; Funding Announcement, revised June 2006. VOJO Funding Announcement, revised June, 2006. VOCA Funding Announcement, 2007-2009. VOCA Funding Guideline Amendment: Mass Violence, 2000. Project STRONG Announcement, May 2005. DCSI JAG Announcements, March 2006. Concept paper formats, March 2006. State Victim Witness Standards and Procedures Manual, April 1999. Victims of Juvenile Offenders VOJO ; Standards and Procedures, effective December 2000. Comprehensive Victim Service Center Standards, Revised February 2001. Monitoring tools for Drug Control and System Improvement DCSI ; , Applications through Project STRONG, VOJO, revised June 2006; RASA, revised June 2006; Victims of Crime Act VOCA ; , revised June 2006; STOP, revised 2005. Pennsylvania Weed and Seed Program Operations Manual, current for 2006. PENNSYLVANIA HOUSING FINANCE AGENCY POLICY STATEMENTS Rental Housing Program 12 Pa. Code, Sections 31.11--31.25 Contact: Holly Glauser-Abel 717.780.3876 ; Owner-Occupied Residential Housing Program 12 Pa. Code, Sections 31.101--31.105 Contact: Kate Newton 717.780.3891 ; Mortgage Loan Program 12 Pa. Code, Sections 31.111--31.117 Contact: Kate Newton 717.780.3891 ; Policy Statement on Homeowners' Emergency Mortgage Assistance Program including Program Guidelines, Act 91 Notice, and list of counseling agencies ; 12 Pa. Code, Section 31.201 et seq. Contact: Daryl Rotz 717.780.3940 ; Privacy Policy Contact: Tony Julian 717.780.3824 ; GUIDANCE MANUALS Development Division PHFA Multifamily Housing Application and Guidelines contains PennHOMES, Taxable and Tax-Exempt Financing and Low Income Housing Tax Credit Guidelines ; PHFA Preprocessing Manual for Projects with Agency Federal HOME Funds PHFA Preprocessing Manual for Projects with Agency Reserve Funds Contact: Kristina Avery 717 ; 780-3876 Technical Services Division Architectural Submission Guide Submission Guide for Small Projects PHFA Preconstruction Meeting Guide General Payout Procedures for Mortgagors & Contractors Contact: Tami Blessing 717 ; 780-3860 or Yolanda Garcia 717 ; 780-4033.
Tricyclic antidepressants amitriptyline, Elavil nortriptyline, Pamelor doxepin, Sinequan imipramine, Yofranil clomipramine, Anafranil protriptyline, Vivactil MAO Inhibitor antidepressants isocarboxazid, Marplan phenelzine, Nardil tranycypromine, Parnate selegiline, Eldepryl, Deprenyl moclebemide, Manerix Plant MAO Inhibitors St. John's Wort Hypericum perforatum ; Yohimbe used for erectile dysfunction ; Syrian Rue Peganum harmala ; --hallucinogen Ayahuasca Banisteropsis caapi ; --hallucinogen Antibiotics Antivirals linezolide, Zyvoxid ritonavir, Norvir Antiemetics ondansetron, Zofran granisetron, Kytril metoclopramide, Reglan SSRIs fluoxetine, Prozac, Sarafem fluvoxamine, Luvox citalopram, Celexa escitalopram, Lexapro paroxetine, Paxil sertraline, Zoloft Other antidepressants venlafaxine, Effexor trazadone, Desyrel mirtazepine, Remeron nefazadone, formerly available as Serzone ; Stimulants amphetamine, methamphetamine Adderall, Dexedrine Desoxyn fenfluramine, Pondimin * dexfenfluramine, Redux * sibutramine, Meridia Drugs of Abuse MDMA Ecstasy methamphetamine cocaine LSD "foxy methoxy" 5-methoxydiisopropyltyptamine ; Miscellaneous L-tryptophan bromocriptine, Parlodel L-dopa, Sinemet!
The Verification Definition Sheet VDS ; is separated into two parts, the header and the body. The header is used for identification and tracking purpose. The VDSs have been separated into the following catergories: ST Structural ME Mechanical EL Electrical CD Command and Data Handling TC Thermal Control EN Environmental MP Material and Parts HE Human Engineering MM Maintainability and Maintenance There are four unique methods of verifying a design requirement: Analysis A ; , Test T ; , Inspection I ; , and Review of Design ROD ; . Each VDS will identify the required method of verification by indicating the method letter identifier, or a combination of identifiers, if more than one method applies. 1 ; Test Test is the determination of properties and performance of an item by mechanical, electrical and environmental functional measurements. This includes analysis of the test data as appropriate. The test method is to be preferred each time is feasible, unless one of the other methods described below can establish an acceptable level of confidence, while being cost and schedule effective 2 ; Analysis.
