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Research Triangle Park, NC: GlaxoSmithKline; 2004. 62 ; Zithromax [prescribing information]. New York, NY: Pfizer Labs; 2004. 63 ; Kmnicef [prescribing information]. North Chicago, IL: Abbott Laboratories; 2005. 64 ; Keflex [prescribing information]. Germantown, MD: Advancis Pharmaceutical Corporation; 2006. 65 ; Ceftin [prescribing information]. Research Triangle Park, NC: GlaxoSmithKline; 2003. 66 ; Claxton AJ, Cramer J, Pierce C. A systematic review of the associations between dose regimens and medication compliance. Clin Ther. 2001; 23 8 ; : 1296-1310. 67 ; Greenberg RN. Overview of patient compliance with medication dosing: a literature review. Clin Ther. 1984; 6 5 ; : 592-599. 68 ; Steele RW, Thomas MP Begue RE. Compliance issues related to the selection of , antibiotic suspensions for children. Pediatr Infect Dis J. 2001; 20 1 ; : 1-5. 69 ; Roos K, Claesson R, Persson U, Odegaard K. The economic cost of a streptococcal tonsillitis episode. Scand J Prim Health Care. 1995; 13 4 ; : 257-260. 70 ; Gilbert DN, Moellering RC, Eliopoulos GM, Sande MA, editors. The Sanford Guide to Antimicrobial Therapy 2006. Sperryville, VA: Antimicrobial Therapy, Inc.; 2006. 14.5. Peri Urban Effect Table 14.7: Reported Impact of Living Near the City N 310 ; Impact Percent Higher land sales 397 Easy access to markets 244 Neglect of land due to labour shortage 211 Negative impact on agriculture 97 Common land reduced 82 Employment Opportunity 35 Other 43 As can be seen in Table, the impact of the city on peri urban communities can be classified as both opportunities and constraints. The highest impact reported by respondents was on higher land sales which could in turn have impacted the availability of agricultural land and the agricultural production. Easy access to markets was another common response followed by the neglect of land due to the shortage of labour in the PUI. 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Author Affiliations: Departments of Medicine Dr Cummings ; and Epidemiology and Biostatistics Drs Cummings, Grady, and Black ; , University of California, San Francisco; Eli Lilly and Co, Indianapolis, Ind Drs Eckert, Krueger, Nickelsen, and Glusman Breast Unit, Royal Marsden NHS Trust Hospital, Sutton, England Dr Powles Department of Epidemiology, University of Pittsburgh, Pittsburgh, Pa Dr Cauley Department of Breast Cancer Medicine, Memorial SloanKettering Cancer Center, New York, NY Dr Norton Center for Clinical and Basic Research, Ballerup, Denmark Dr Bjarnason Department of Surgery Dr Morrow ; and the Robert H. Lurie Cancer Center Dr Jordan ; , Northwestern University Medical School, Chicago, Ill; Lombardi Cancer Center, Georgetown University Medical Center, Washington, DC Dr Lippman and European Institute of Oncology, Milan, Italy Dr Costa ; . Financial Disclosures: Drs Cummings, Grady, Powles, Cauley, Norton, Bjarnason, Morrow, Black, Costa, Lippman, and Jordan received research support or honoraria for speaking, served on the Oncology Advisory board for, or served as a consultant for Eli Lilly & Co. Drs Ecker, Krueger, Nickelsen, and Glusman are or have been employees of or own stock in Eli Lilly & Co, Indianapolis, Ind. Drs Cummings, Cauley, Black, and Costa have received research support from Merck & Co, Inc, West Point, Pa. Drs Grady, Cauley, and Black have received research funding or have served as a consultant for Wyeth-Ayerst, Philadelphia, Pa. Dr Black has received honoraria from Procter & Gamble, Cincinnati, Ohio. Drs Cummings and Jordan have served as consultants for SmithKline Beecham Pharmaceuticals, Philadelphia. Drs Cummings and Grady have been consultants for Pfizer Inc, New York, NY. Dr Cauley is negotiating research support from Roche Laboratories, Nutley, NJ. Drs Morrow and Jordan are on the speakers bureau for Zeneca Pharmaceuticals, Wilmington, Del. Funding Support: Eli Lilly & Co provided funding for the study. Acknowledgment: We thank Ron Knickerbocker, MD, Leo Plouffe, MD, Fred Cohen, MD, and Bruce Ettinger, MD, for their contributions and advice, and we thank Ms Trisha Hue, BS, of the University of California, San Francisco, for her thoughtful editing and stromectol. Variables contributing to the selection of antibiotics for children.7 Specific variables evaluated were palatability, cost, duration of therapy, and dosing interval. Suspension characteristics that were evaluated included appearance, smell, texture, taste, and aftertaste. Amoxicillin Amoxil ; served as the standard to which the other antibiotics were compared, chiefly due to its good taste, low cost, and widespread use for treating otitis media in the pediatric population. In addition to amoxicillin, evaluated antibiotic suspensions included cefdinir Mnicef ; , trimethoprim-sulfamethoxazole Bactrim, Septra ; , trimethoprim Primsol ; , cefpodoxime Vantin ; , azithromycin Zithromax ; , cefuroxime Ceftin ; , clarithromycin Biaxin ; , cefixime Suprax ; , loracarbef Lorabid ; , amoxicillin clavulanate Augmentin ; , and ciprofloxacin Cipro ; . Individuals with a history of allergy to any of the antibiotics, pregnant women and those with upper respiratory infections altered smell or taste ; were excluded from participation. Before evaluating the antibiotics, each participant spent time briefly discussing the implications of cost, duration of therapy and dosing intervals in the selection of antibiotics. Dr. Nuttall graduated from the University of Bristol in 1992. After three years in general practice he joined the University of Edinburgh, where he gained the RCVS CertVD and a PhD in canine atopic dermatitis. 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In summary, there is considerable overlap with respect to type and duration of symptoms experienced by PAR and SAR patients. Urticaria is rarely a serious illness, however, it is a common complaint. Up to 10% of the population lifetime prevalence ; will have an episode of urticaria all types ; , although it is difficult to obtain precise figures. The newest conducted studies point to a female: male ratio of about 1.5: 1.0. Urticaria may be Acute duration of episodes of hives less than six weeks ; or Chronic duration of urticaria for six or more weeks ; . Chronic Idiopathic Urticaria CIU ; with or without angioedema is defined as the occurrence of frequent urticaria characterised by episodic or persistent wheals, which recur for a minimum of 6 weeks but frequently over months or years. The true incidence of CIU remains unclear. The percentages vary from 0.25-5% in the entire population. CIU patients, in whom history and laboratory tests fail to disclose an underlying cause, account for 80-90% of all cases of chronic urticaria. Though the cause of CIU is unknown, mast cell mediators, of which histamine is the best known, play an important role in the pathogenesis of this disease. The symptoms of CIU may be extremely troublesome for many subjects and may cause significant impairment of their quality of life. The lesions are associated with severe pruritus and may be accompanied by a stinging or somewhat painful prickling sensation. The histamine H1-receptor antagonists are important first-line medications for the symptomatic treatment of urticaria. However, the use of the classical H1 antihistamines is often accompanied by undesirable side effects, particularly central nervous system CNS ; symptoms such as sedation and anticholinergic effects such as dry mouth. The development of the nonsedating second-generation H1 antagonists, largely free of the side effects of older antihistamines has been a major advantage for the symptomatic treatment of urticaria. Pruritus is the hallmark symptom of urticaria and is generally responsive to the administration of an antihistamine. Other efficacy assessments relevant to urticaria include number and size of hives, interference with sleep and daily activities, overall condition and therapeutic response. 2. Part II: Chemical, pharmaceutical and biological aspects and tetracycline. Clinical trials in children with acute diarrhoea, using the standard recommended dose and double dosages, have not shown any effect on stool output. Esearchers, doctors, and patients from around the world gathered at Brussels in September for this conference, organized by Dr. Kenny MeMeirleir. He is noted for his work on the RNase-L antiviral pathway and the drug Ampligen, which were among the many topics covered at the conference. Discussions also included subgrouping of patients, treatments, memory and learning, CFIDS in adolescents, exercise capacity, and GWI Gulf War Illness. 16 8. Moghadasian, M.H., G. Salen, J.J. Frohlich and C.H. Scudamore. 2002. Cerebrotendinous xanthomatosis: a rare disease with diverse manifestations. Arch. Neurol. 59: 527-529. 9. Salen, G., P.O. Kwiterovich Jr., S. Shefer, G.S. Tint, I. Horak, V. Shore, B. Dayal, and E. Horak. 1985. Increased plasma cholestanol and 5 alpha-saturated plant sterol derivatives in subjects with sitosterolemia and xanthomatosis. J. Lipid Res. 26: 203-209. 10. Salen, G., E.H. Ahrens, and S.M. Grundy. 1970. Metabolism of man. J. Clin. Invest. 49: 952-967. 11. Salen, G., S. Shefer, L. Nguyen, G.C Ness, G.S. Tint, and V. Shore. 1992. Sitosterolemia. J. Lipid Res. 33: 945-955. 12. Lutjohann, D., I. Bjorkhem, U.F. Beil, and K. von Bergmann. 1995. Sterol absorption and sterol balance in phytosterolemia evaluated by deuterium-labeled sterols: effect of sitostanol treatment. J. Lipid Res. 36: 1763-1773. 13. Shulman, R.S., A.K. Bhattacharyya, W.E. Connor, D.S. Frederickson. 1976. sitosterolemia and xanthomatosis. N. Engl. J. Med. 294: 472-483. 14. Salen, G., V. Shore, G.S.Tint, T. Forte, S. Shefer, I. Horak, E. Horak, B. Dayal, L. Nguyen, A.K. Batta, F.T Lindgren, and P.O. Kwiterovich Jr. 1989. Increased sitosterol absorption, decreased removal, and expanded body pools compensate for reduced cholesterol synthesis in sitosterolemia with xanthomatosis. J. Lipid Res. 30: 1319-1330. -sitosterol in. Omnicef had another outstanding quarter with sales growth of more than 70%. This is its 17th consecutive quarter of double- digit growth. We continue to expect strong double- digit growth for Omnicef for the fourth quarter and for the full- year. Where to buy Omnicef In order to hare omnicef and birth control overestimated racism, effects of doxycycline must be disabled and dipyridamole and buy prograf. Galvus vildagliptin ; , a new oral treatment for type 2 diabetes, is expected to be made available in Europe starting in the first half of 2008. European health authorities announced in November 2007 their support for changes proposed by Novartis to prescribing information that would reduce the recommended daily doses to 50 mg once-daily or 50 mg twice-daily in combination with various other oral anti-diabetes medicines. EU approval has also been received for Eucreas, a single-tablet combination of Galvus with the oral anti-diabetes medicine metformin, which will also have amendments to its labeling before launch. In the US, we are continuing discussions with the FDA on steps needed for approval after having received an ``approvable letter'' in February 2007 that included a request for additional clinical trial data. Vaccines and Diagnostics Division Net sales rose 52% + 47% lc ; thanks to an excellent performance driven by a rise in sales of TBE tick-borne encephalitis ; , pediatric and seasonal influenza vaccines as well as NAT nucleic acid test ; blood testing products. On a comparable 2006 full-year basis, net sales were up 25% including unaudited net sales from Chiron for four months in the year-ago period before the April 2006 acquisition ; . Sandoz Division Net sales advanced 20% + 13% lc ; thanks to dynamic growth in the US and strengthened positions in fast-growing markets, particularly in Eastern Europe. Sandoz provided an incremental contribution of more than billion to annual net sales. Contributions from recently launched products, including ``difficult-to-make'' generics such as metoprolol succinate ER Toprol-XL ; and cefdinir Omnicef ; , supported the 27% increase in US net sales, which also benefited from the launch of an authorized generic version of amlodipine benazepril Lotrel ; . Several other countries contributed to growth, led by Russia, France, Canada, Poland, Turkey, China and Brazil. Consumer Health Division Strong performances from OTC and Animal Health Business Units underpinned the 11% + 6% lc ; increase in net sales, driven by the increased focus on strategic brands, new product launches and expansion in emerging markets and Japan. CIBA Vision net sales were higher, supported by a resumption of contact lens and lens-care product deliveries in 2007 following shortages in 2006. Discontinued Consumer Health Division operations Following recent divestments, the financial results of the Medical Nutrition including Nutrition & Sant ; and Gerber Business Units are reported as ``Discontinued operations'' in both 2007 and 2006. A e combined total of .7 billion in net sales was recorded in 2007 prior to the divestments of Medical Nutrition as of July 1, 2007 ; and Gerber as of September 1, 2007. It is not effective in terminating an existing pregnancy. History of Omnicef Suicide cannot be defined as a mental disorder, the various risk factors--especially the presence of mood disorders--that predispose young people to such behavior are given special emphasis in this section, as is a discussion of the effectiveness of various forms of treatment. The evidence is strong that over 90 percent of children and adolescents who commit suicide have a mental disorder, as explained later in this section. Major depressive disorder is a serious condition characterized by one or more major depressive episodes. In children and adolescents, an episode lasts on average from 7 to 9 months Birmaher et al., 1996a, 1996b ; and has many clinical features similar to those in adults. Depressed children are sad, they lose interest in activities that used to please them, and they criticize themselves and feel that others criticize them. They feel unloved, pessimistic, or even hopeless about the future; they think that life is not worth living, and thoughts of suicide may be present. Depressed children and adolescents are often irritable, and their irritability may lead to aggressive behavior. They are indecisive, have problems concentrating, and may lack energy or motivation; they may neglect their appearance and hygiene; and their normal sleep patterns are disturbed DSM-IV ; . Despite some similarities, childhood depression differs in important ways from adult depression. Psychotic features do not occur as often in depressed children and adolescents, and when they occur, auditory hallucinations are more common than delusions Ryan et al., 1987; Birmaher et al., 1996a, 1996b ; . Associated anxiety symptoms, such as fears of separation or reluctance to meet people, and somatic symptoms, such as general aches and pains, stomachaches, and headaches, are more common in depressed children and adolescents than in adults with depression Kolvin et al., 1991; Birmaher et al., 1996a, 1996b ; . Dysthymic disorder is a mood disorder like major depressive disorder, but it has fewer symptoms and is more chronic. Because of its persistent nature, the disorder is especially likely to interfere with normal adjustment. The onset of dysthymic disorder also called dysthymia ; is usually in childhood or. The site offers colorful animation and audio clips to help patients and caregivers understand cell division , tumor cavity reservoirs , vp shunts and many of the other procedures and treatments relating to brain tumors. Omnicef cost It was later withdrawn from the market due to high risk of rhabdomyolysis discussed later ; . In summary, the incidences of myopathy, mild or severe, reported in clinical trials are between 0.1 percent and 5.0 percent, depending on dose and type of statin. However, many patients excluded from the trials receive these agents in clinical practice. Also, patients in clinical trials are generally better informed, and monitored very closely as compared to those in a "real-world" setting.151, 152 Therefore, these incidences may be underestimated in clinical trials compared to actual rates of myopathy in "real-world" situations.153, 154, 155 The case of cerivastatin is an example where the incidence was low in clinical trials but the drug was later withdrawn from market due to increased rates of rhabdomyolysis. The next part looks at the life-cycle of cerivastatin from its marketing approval to its withdrawal. SB 465, McPherson. Santa Cruz County Regional Transportation Commission. 1 ; Existing law creates and prescribes the membership and powers of the Santa Cruz County Regional Transportation Commission. This bill would revise the membership of the governing body of the commission. To the extent that this revision would establish additional duties upon local governmental entities, the bill would impose a state-mandated local program. The bill would revise the power of the commission, to permit it to exercise 1 ; the power of eminent domain, 2 ; the power to preserve, acquire, construct, improve, and oversee multimodal transportation projects and services on rail rights-of-ways with Santa Cruz County to facilitate recreational, commuter, intercity, and intercounty travel, and 3 ; the authority to contract for any services to accomplish its purposes. 2 ; The California Constitution requires the state to reimburse local agencies and school districts for certain costs mandated by the state. Statutory provisions establish procedures for making that reimbursement. This bill would provide that no reimbursement is required by this act for a specified reason. The people of the State of California do enact as follows: SECTION 1. Section 67940 of the Government Code is amended to read: 67940. a ; The Santa Cruz County Regional Transportation Commission is hereby created, as a local area transportation planning agency, and not as part of the executive branch of state government, to provide regional transportation planning and development for the area of Santa Cruz County. The commission may be known by any other name it chooses and is the legal successor to the Santa Cruz County. A: To apply to all categories with brand and generic versions on different sides of the PDL: Prior Authorizations for non-preferred brands or in certain cases non-preferred generic form -- 1. Requests will be approved for patients that show reduced objective outcomes on the preferred version relative to the non-preferred version. 2. Requests will be approved for patients experiencing side effects on the preferred generic version only if the side effect has not been reported in the literature for the brand version. The completion and submission of the medwatch form will then also be required. B: To apply to all requests for non-preferred brands and other drugs with PA conditions for non FDA approved indications. Decisions will be made on a case by case basis until the DUR committee is able to review the evidence and make a recommendation. Interim approvals and DUR recommendations for approval of a drug for a non FDA approved indication will require a minimum of two published, peer reviewed, non contradicted, double-blinded, placebo-controlled, randomized studies establishing both safety and efficacy. C: PDL drugs may also be affected by dose consolidation requirements. See list of limited drugs start on the last page of PDL. D: 1. The minimum trial periods for each preferred and step-order drug is two weeks, unless otherwise stated within specific PDL drug categories. 2. A trial will not be considered valid if non preferred products were readily available paid by override, cash, or samples ; . 3. Certain drug trials, such as with preferred narcotics, may require evidence that the preferred drugs were actually tried example: with urine drug tests ; . 4. Trials withl less than a two week duration will be reviewed on a case-by-case basis. E: Other Criteria: Drugs that must be submitted on specific prior authorization forms may contain additional criteria that has not been repeated below in this document. ASSORTED ANTIBIOTICS BETA-LACTAMS CLAVULANATE COMBO'S AMOXICILLIN AMOXIL1 AMPICILLIN AUGMENTIN AUGMENTIN ES-600 SUSR AUGMENTIN XR TB12 BEEPEN BICILLIN L-A SUSP DICLOXACILLIN SODIUM CAPS DYNAPEN SUSR GEOCILLIN TABS OXACILLIN SODIUM SOLR PENICILLIN V POTASSIUM TICAR SOLR TIMENTIN SOLR TRIMOX UNASYN SOLR VEETIDS ZOSYN CEPHALOSPORINS CEFADROXIL HEMIHYDRATE CEFAZOLIN SODIUM SOLR CEFUROXIME AXETIL TABS CEFZIL CEPHALEXIN MONOHYDRATE DURICEF SUSR FORTAZ SOLR KEFZOL SOLR MAXIPIME SOLR OMNICEF ROCEPHIN SUPRAX VANTIN MACROLIDES ERYTHROMYCIN'S BIAXIN XL BIAXIN 1. QL ZPAC 250mg 6 i t th Preferred drugs must be tried and failed due to lack of efficacy or intolerable side effects before non-preferred drugs will be approved, unless an acceptable clinical exception is offered on th P diti th t t ifi t t ti CECLOR1 CEDAX CEFACLOR1 CEFADROXIL MONOHYDRATE TABS CEFTIN DURICEF TABS FORTAZ SOLN KEFLEX CAPS TAZICEF SOLR Use PA Form # 20420 1. Both brand and generic are Preferred drugs must be tried and failed due to lack of efficacy or intolerable side effects before non-preferred drugs will be approved, unless an acceptable clinical exception is offered on clinically non-preferred. the Prior Authorization form, such as the presence of a condition that prevents usage of the preferred drug or a significant potential drug interaction between another drug and the preferred drug s ; exists. Use PA Form# 20420 AMOXICILLIN POTASSIUM CLA CHEW AMOXICILLIN POTASSIUM CLA SUSR AMOXICILLIN POTASSIUM CLA TABS AMOXIL 500mg TABS PRINCIPEN CAPS2 PRINCIPEN SUSR 1. Amoxil 500mg tabs are non- Preferred drugs must be tried and failed due to lack of efficacy or intolerable side effects before non-preferred drugs will be approved, unless an acceptable clinical exception is offered on the Prior Authorization form, such as the presence of a condition that prevents usage of the preferred drug or a significant potential drug interaction between another drug and the preferred preferred. All other Amoxil drug s ; exists. products are preferred. 2.Principen 250 mg is available without PA. With the consent of the victim, the physician gives a copy of the certificate containing the victim's name: to HCR to the protection officer only ; if the victim is a refugee or displaced, so that protection measures may be put in place for the individual; to ICRC if the victim is a victim of war or a prisoner. Without the consent of the victim, the physician may give a copy of the certificate to HCR or ICRC, but without revealing the identity of the victim concretely, the sections "family name, first name and precise address" should not appear. Omnicef cream Neomycin Polymyxin Gramicidin Neomycin Polymyxin HC Neoral Neotron-S Neo-Tuss Nephronex Nervidox Nescon-PD Neumega Neuro-B12 Neutragard Neutragard Advanced Nexavar PA ; Niaspan Nicardipine HCL Nifediac CC Nifedical XL Nifedipine Nifedipine ER Nilandron Nitrek Nitro-Bid Nitro-Dur 0.3mg hr Nitro-Dur 0.8mg hr Nitrofurantoin Macrocrystal Nitrofurantoin Monohyd Macro Nitroglycerin Nitroglycerin Transdermal Nitroglyn Nitrolingual Nitroquick Nitro-Time Nizatidine Nohist Nohist-A Nohist-EXT Nora-BE Norel DM Norethindrone Acetate Norpace CR 100mg Nortrel Nortriptyline HCL Nortuss-DE Nortuss-EX Norvasc Norvir Novagesic Novolog Novolog Mix 70 30 Nuhist Nulytely With Flavor Packs Nu-Natal Advanced Nutracare Nutricion Porvida Nutrifac ZX Nutrinate Nutrispire Nutropin PA ; Nutropin AQ PA ; Nutropin Depot PA ; Nuvaring Nystatin Nystatin w Triamcinolone Ny-Tannic Octreotide Acetate Ofloxacin Ogestrel Omeprazole PA ; Omnicef Omnihist L.A. Omnii Med One Flow Fvc Optichamber Orap PA 6 yrs or under ; Orphenadrine Citrate Orphenadrine Compound. Omnicef price 14 are medicare-approved drug discount cards available now. 178. Stambrook M, Moore AD, Peters LC, et al. Effects of mild, moderate and severe closed head injury on longterm vocational status. Brain Inj 1990; 4 2 ; : 18390. [~] 179. Satz P, Zaucha K, Forney DL, et al. Neuropsychological, psychosocial and vocational correlates of the Glasgow Outcome Scale at 6 months post-injury: a study of moderate to severe traumatic brain injury patients. Brain Inj 1998; 12 7 ; : 55567. [ + ] 180. Asikainen I, Nybo T, Muller K, et al. Speed performance and long-term functional and vocational outcome in a group of young patients with moderate or severe traumatic brain injury. Eur J Neurol 1999; 6 2 ; : 179 85. [~] 181. Ryan TV, Sautter SW, Capps CF, et al. Utilizing neuropsychological measures to predict vocational outcome in a head trauma population. Brain Inj 1992; 6 2 ; : 17582. [x] 182. Sherer M, Bergloff P, Levin E, et al. Impaired awareness and employment outcome after traumatic brain injury. J Head Trauma Rehabil 1998; 13 5 ; : 5261. 183. Bricout JC, Bentley KJ. Disability status and perceptions of employability by employers. Soc Work Res 2000; 24 2 ; : 8795. [x] 184. Johnstone B, Vessell R, Bounds T, et al. Predictors of success for state vocational rehabilitation clients with traumatic brain injury. Arch Phys Med Rehabil 2003; 84 2 ; : 1617. [x] 185. Sherer M, Nick T, Sander A, et al. Race and productivity outcome after traumatic brain injury: influence of confounding factors. J Head Trauma Rehabil 2003; 18 5 ; : 40824. [~] 186. NHS Centre for Reviews and Dissemination. Modified work and return to work: a review of the literature structured abstract ; . Database of Abstracts of Reviews of Effects 2006 Issue 1. Original article: Journal of Occupational Rehabilitation. 1998; 8 2 ; : 11339. 187. Schneider JC. Is supported employment cost effective? A review. The International Journal of Psychosocial Rehabilitation 2003; 7: 14556. [~] 188. Wehman P, Kregel J, Keyser-Marcus L, et al. Supported employment for persons with traumatic brain injury: a preliminary investigation of long-term follow-up costs and program efficiency. Arch Phys Med Rehabil 2003; 84 2 ; : 1926. [x] 189. Wehman P, Kreutzer J, West M, et al. Return to work for persons with traumatic brain injury: a supported employment approach. Arch Phys Med Rehabil 1990; 71 13 ; : 104752. [x] 190. Hibbard MR, Gordon WA, Flanagan S, et al. Sexual dysfunction after traumatic brain injury. NeuroRehabilitation 2000; 15 2 ; : 10720. 191. Medlar T. Sexual counseling and traumatic brain injury. Sex Disabil 1993; 11 1 ; . [~] 192. Dolberg O, Klag E, Gross Y, et al. Relief of serotonin selective reuptake inhibitor induced sexual dysfunction with low-dose mianserin in patients with traumatic brain injury. Psychopharmacology 2002; 161 4 ; : 4047. [~ x] 193. Heller L, Keren O, Aloni R, et al. An open trial of vacuum penile tumescence: constriction therapy for neurological impotence. Paraplegia 1992; 30 8 ; : 5503. [~] 194. Simpson G, Blaszczynski A, Hodgkinson A. Sex offending as a psychosocial sequela of traumatic brain injury. J Head Trauma Rehabil 1999; 14 6 ; : 56780. [~] 195. Bezeau SC, Bogod NM, Mateer CA. Sexually intrusive behaviour following brain injury: approaches to assessment and rehabilitation. Brain Inj 2004; 18 3 ; : 299313. [~ ] 196. Tyerman A, Booth J. Family interventions after traumatic brain injury: a service example. NeuroRehabilitation 2001; 16 1 ; : 5966. [x] 197. Britton K. Medroxprogesterone in the treatment of aggressive hypersexual behaviour in traumatic brain injury. Brain Inj 1998; 12 8 ; : 7037. [x] 228. 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