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Such as nukes nucleoside analogues ; and non-nukes non-nucleoside reverse transcriptase inhibitors ; . Combinations such as this are called highly active antiretroviral therapy, or HAART. In order for indinavir to be effective it must be taken with at least two other anti-HIV drugs. For more information on HAART, see CATIE's Practical Guide to HAART for People Living with HIV AIDS at : catie PG HAART e.nsf For many people with HIV AIDS PHAs ; , the use of HAART has increased their CD4 + cell counts and decreased the amount of HIV in their blood viral load ; . These beneficial effects help to reduce the risk of developing a life-threatening infection. Neither indinavir nor any other anti-HIV medication is a cure for HIV AIDS. It is therefore important that you do the following: see your doctor regularly so that he she monitors your health continue to practice safer sex.
Antiretroviral drugs back nevimune nevimune tablets nevimune oral suspension warning severe, life-threatening skin reactions, including fatal cases, have occurred in patients treated with nevirapine.
Developed at a time when AZT was the only available treatment option, Johnston's HIV AIDS Wheel follows the flow of the Medicine Wheel, incorporating the medical knowledge of HIV disease into a cycle of life stages and states of being. These elements speak to the inter-connected relationships and forces.
If this service is available, PEP is usually given for 28 days as a mono, bi- or a triple-therapy of a combination of 1, 2, or 3 anti-retroviral drugs ARV ; . There are many problems and issues surrounding the prescription of PEP, not the least of which is the difficulty of counselling the woman on HIV issues at a time like this. If you wish to know more about PEP, see the Further Readings. If it is possible in your setting for the woman to receive PEP, refer her as soon as possible up to 72 hours after the rape ; to the relevant centre. If she presents after this time, counsel the survivor on VCT services if available in your area. Prevent pregnancy Taking emergency contraceptive pills ECP ; within 72 hours of unprotected intercourse will reduce the chance of a pregnancy between 74-85%, depending on the regimen chosen and the timing of starting the course see Annex 7 ; . As described by WHO, "emergency contraceptive pills ECPs ; work by interrupting a woman's reproductive cycle by delaying or inhibiting ovulation, blocking fertilisation or preventing implantation of the ovum. ECPs do not interrupt or damage a pregnancy and thus are not considered a method of abortion". Some people believe that ECPs are abortifacients. Health workers holding such belief may be precluded from providing this treatment. Women who request this service should be offered counselling so as to reach an informed decision. A health worker who is willing to prescribe ECPs should always be available to prescribe them to rape survivors who may wish to use them to prevent pregnancy. If the survivor is a young child who has reached menarche, also discuss EC with her and her mother guardian who can help her to understand and take the regimen, if indicated If an early pregnancy is detected at this stage, either with a pregnancy test or by completing the history and examination see Steps 3 and 5 ; , it can be helpful for the woman to know that a confirmed pregnancy is not the result of the rape. There is no evidence of contraindication to giving ECPs at the same time as antibiotics.
The goal of drug treatment is to achieve a period of negative energy balance followed by a balance of energy intake and output with minimal adverse effects. Patients frequently achieve the initial negative energy balance but it is too often followed by a period of positive energy balance. This is, among other things, secondary to the physiologic changes that take place with the initial weight loss and may lead to resistance of further weight loss. It has been documented that exercise may partially ameliorate some of this problem with greater sustained weight loss for 1 year in exercisers 26, 27 ; . Negative energy balance can be obtained by decreased energy intake or increased energy expenditure, or a combination of both. As the medications are discussed, the mechanisms of action are noted regarding the effect on food intake, alteration of metabolism or increased energy expenditure. Chapter 5 Drug Treatment of Obesity 109.
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Muchas personas que reciben tratamiento contra el VIH experimentan cambios en su cuerpo. Algunas personas que reciben medicamentos contra el VIH llamados agentes antirretrovirales ; pueden aumentar de peso en el torso, desarrollar acumulacin de tejido graso en distintas partes del cuerpo, o aumentar de peso en la parte superior de la espalda y del cuello.Tanto en hombres como en mujeres, los depsitos de grasa en el pecho pueden causar su agrandamiento. Esto se denomina lipohipertrofia.1.
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Corresponding author. Tel.: + 1 615 322 fax: + 1 615 343 E-mail address: hakan.sundell vanderbilt H.W. Sundell ; . 1 Present address: Department of Women and Child Health, G teborg University, The Queen Silvia Children's Hospital, SE-416 o 85 G teborg, Sweden. o 2 Present address: Department of Women and Child Health, Karolinska Institute, E-171 76 Stockholm, Sweden.
Webmd privacy policy health extras q& a: ask our health experts a question now » find a therapist » google refined search » menopause topics osteoporosis menopause hormone therapy treatment for hot flashes premature menopause menopause and sex menopause rss ask the experts webmd resources doing enough for your bones and risperidone.
Shock number two: the figure was groping lamentably and blindly in the undergrowth, and when, for an instant, the face was turned extreme of muscular tension about them.
Interactions with this drug may occur with the following: cholestyramine questran ; isoniazid rifater ; phenytoin dilantin ; blood thinners coumadin ; zidovudine retrovir ; birth control pills non-steroidal anti-inflammatory drugs-commonly called nsaids is there a problem if i have another disorder or disease and roxithromycin.
Objective: To investigate the effect of antisense TGF-1 gene on the mesangial hyperplasia by unilateral nephrectomy in diabetic rats. Methods: Transfection with TGF-1 antisense oligonucleotide to the mesangial cells from unilateral diabetic rats with the lipofectamine was carried out by transgenic technique. The recombinant antisense TGF-1 retroviral vector plasmid by virus packaging cell PA317 was packed when the virus titer was also detected by NIH 3T3 cell, having the mesangial cells of unilateral diabetic rats infected with the highest titers virus supernatant. The TGF-1 mRNA expression of mesangial cells and other extracellular matrix such as collagen IV and fibronectin with RT-PCR was also measured, and the TGF-1 protein expression was measured with ELISA. Results: Both renal hypetrophy of mesangial cells and mesangial expansion of DN were inhibited by both antisence TGF-1 oligonucleotide and recombinant antisence TGF-1 retroviral expressing plasmid leading to a decrease not only in the expression of TGF-1 protein but also in the mRNA expression of TGF-1 mRNA. Furthermore, the matrix expression was also decreased, such as fibronectin and collagen IV. Conclusion: It suggests that TGF-1 antisense gene can prevent diabetic nephropathy progress.
Show a prostaglandin-dependent mechanism in the regulation of leptin secretion. This negative finding fits with our data, because the effect of Ang II was completely blocked by a specific AT1 receptor antagonist, whereas the generation of prostaglandins, in particular prostacyclin, has been reported to be caused by an AT2 receptormediated pathway 16 ; . Our data support the idea that Ang II may act as a positive regulator of leptin production in adipocytes. We showed for the first time that this effect is mediated through the ERK1 2 signaling pathway. These experimental data are consistent with studies in vascular smooth muscle cells where Ang II has been found to exert a variety of actions on atherosclerosis through this pathway 17 ; . ERK1 2 phosphorylation represents an early response to Ang II and may be involved in the expression of cytokines 14 ; . In addition, in a recently established cell line of brown adipocytes derived from mouse hibernoma, the transcriptional control of leptin expression by insulin was found to partially involve a mitogen-activated protein kinase dependent mechanism 18 ; . A recent study showed that angiotensinogen-deficient mice exhibit the same leptin levels compared with wild-type mice 19 ; , which is contrary to our findings. However, one has to keep in mind that the regulation of leptin is complex and includes many other factors, such as glucocorticoids or insulin. Thus, the physiological effect of Ang II on leptin secretion may be admixed or superimposed by such regulators. In conclusion, our observation that Ang II stimulates leptin expression in human adipose tissue may represent a and reboxetine.
Public health benefits of screening for DS in socioeconomically deprived areas are small because of low uptake of amniocentesis Ford and others 1998 ; . With lower uptake rates of amniocentesis, both efficacy and financial cost-effectiveness are adversely affected as a result of low detection rates, and the number of unaffected fetal losses decreases. It is also important to note that, in some countries, many women may not have access to prenatal care or may not seek prenatal care and prenatal testing. In such areas, programs that try to reduce DS prevalence will have limited success, especially if a population at greater risk of DS is not tested. Cost-effectiveness is often measured per DS birth averted since reduction in DS prevalence is the ultimate goal of prenatal testing. In many cultures, an abortion is not an acceptable option. Acceptance of elective termination of pregnancy may also vary across ethnicities and other subgroups within a given country. A study in California found the uptake of termination following the DS diagnosis varied from 47.5 percent for Hispanics to 65.8 percent for whites and 70.8 percent for Asians Cunningham and Tompkinison 1999 ; . If few families decide to terminate pregnancy to avoid having a child with severe disability, cost-effectiveness per DS birth averted will be adversely affected, and the screening program may fail to reduce the birth prevalence of DS. If a large percentage of families are opposed to induced abortion of fetal DS, the uptake of amniocentesis also will be low, for example, zidovudine retrovir.
Polly Clayden, HIV i-Base The Collaborative HIV Paediatric Study CHIPS ; is a multicentre cohort of children in the UK and Ireland participating in PENTA trials since 1996. A study reported in the 24 September issue of AIDS evaluates the effect of age, pre-HAART CD4 percentage CD4% ; and plasma HIV-1 RNA on response to highly active antiretroviral therapy HAART ; in treatment nave children. The investigators reported that on 1 June 2003, 692 children had enrolled in CHIPS and 462 had received HAART. Of these 324 were drug nave when initiating HAART regimens and 265 82% ; had both CD4 and viral load values pre-HAART and therefore eligible for this evaluation. Seventy-seven 29% ; children were less than 2 years old. 39 17% ; under one year, 49 18% ; were over 9 years. One hundred and thirty-eight children 52% ; had CD4% of 15% or lower at HAART initiation. The investigators reported that at 6 months, 181 86% ; of children had higher CD4% than at baseline. In univariate and multivariate analyses, adjusted for confounding factors, 10% CD4% increase was more likely at younger age [OR 0.84 per year, p 0.001] and lower pre-HAART CD4% [OR, 0.67 per 5% higher, p 0.001 ; , but was not related to pre-HAART viral load. Effects of AIDS stage, calendar year of HAART initiation or HAART regimen were not significant Younger age was also associated with a higher chance of achieving CD4% of 30% at 6 months. Children starting with a four drug regimen were more likely to achieve CD4% 30% at 6 months at all ages OR, 5.48; 95% CI, 1.18-25.5; p 0.03 ; . Conversely older children were more likely to achieve HIV-1 RNA suppression, 400 copies ml at 6 months p 0.03 ; , and this was unrelated to pre-HAART HIV-1 RNA or CD4%. Children initiating HAART with 4 drugs had a greater likelihood of suppression adjusted OR, 3.07; 95% CI, 1.04-9.08; p 0.04 ; . Only 57 27% ; children achieved HIV-1 RNA 50 copies at 6 months and the likelihood was also greater in older children OR, 1.09 per year of age; 95% CI, 1.01-1.18; p 0.02 ; . CD4% and HIV-1 RNA results were available for 149 children at 24 months and the investigators report that predictors were similar to 6 months results for CD4% increases over 10% at 24 months overall rate 62% vs 38% at 6 months ; : initiation of HAART at younger age OR, 0.87 per year, p 0.02 ; or with lower CD4% OR, 0.60 per 5% higher baseline, p 0.0001 ; . There were no predicting factors for viral load suppression 400 copies ml at 24 months overall rate 54% vs 60% at 6 months ; . The authors write: "The findings from our study suggest that there are critical differences in the predictors of immunological and virological responses to HAART in previously untreated children and adults. Specifically, in children there are substantial and sodium.
If client answers YES, perform physical exam or refer. If she has serious active liver disease jaundice, painful or enlarged liver, viral hepatitis, liver tumor ; , do not provide POPs. Refer for care. Help her choose a method without hormones. If the client answers YES, refer her to the clinic physician and give her condoms spermicide to use in the meantime. If client answers NO, continue with question 4. If client answers YES, you can give her POPs now with instructions on when to start-- when the baby is six weeks old. If client answers YES, assess if she is not likely to be pregnant but has unexplained vaginal bleeding that suggests an underlying medical condition. You can provide POPs since neither the underlying condition nor its assessment will be affected. Assess and treat any underlying condition as appropriate, or refer. Reassess POP use based on findings, for example, protease.
PBGH's Whipple reports that 10 employers had committed to participate in the diabetes challenge as of the beginning of the year, and those companies were to begin issuing invitation letters to selected workers by late January. The organization began signing up pharmacist coaches in February and plans to start reporting preliminary data by fall. "[Pharmacists] will need to go through programs to be certified to work with diabetes patients, " Whipple says and stavudine.
The test material was prepared as solutions in corn oil at the following concentrations to achieve the desired dose levels. Group Dose group Concentration Volume mg kg day mg ml ml kg I 250 62.5 4 III 500 125 4 IV 1000 250 4 ; valid without restriction 10 ; : : Sub-acute Rat Male female Sprague-Dawley Dermal Six hours daily Daily, five days each week for four weeks 525, 1050 & 2100 mg kg day Yes, concurrent vehicle 2100 mg kg bw 1977 Yes R960002575 Male and female Sprague-Dawley rats aged approximately 7 and 9 weeks respectively were used in this study. The test material was applied to the shorn skin of groups of five male and five females for each dose level. Additionally, a group of five male and five females served as vehicle controls and for these mineral oil alone was applied. The test sites were covered with an occlusive dressing which was left in place for six hours. After this time, the dressings were removed and any residual test material was removed from the skin using a gauze and mineral oil. This treatment was continued daily, five days each week for four weeks. Animals were observed twice daily for clinical signs of toxicity. A more thorough examination was undertaken weekly and this included a detailed physical examination for signs of local or systemic toxicity, pharmacological effects and palpation for tissue masses. Body weights and food intakes were recorded weekly. At the end of the study, and after overnight fasting, animals were killed and blood samples were collected for the following hematological and serum chemistry investigations. Hematology Hemoglobin concentration Hematocrit Erythrocyte count 33 47.
When Vitou arrived high quality nutrition and care, a several years ago, he was small skin-and-bones child soon completely listless, could not lift becomes a lively member of our his head, had huge swollen orphanage family. glands, fever, and a cough. I Our children at the told our doctor that I doubted if Orphanage take their meds at 8 the child could survive. Today and 8 pm, so routinely it he is busy healthy five year causes no comment from anyone. old, on antiretrovirals for HIV, Originally, 4 years ago, we bought who rides his bike in the yard the medications through Maryknoll, with the other "older " kids. No but since December 22, 2005 the one visiting the Orphanage Clinton Foundation has funded all would identify him, or any of the identified and registered children other HIV infected children as completely for their meds. Most of having a serious illness our children are on a "cocktail " of HIV AIDS is a major nevirapine, lamivudine and problem in Cambodia where stavudine; one child, who has had Some of our HIV infected children at Roteang Orphanage. levels are second only to those some resistance, is on other meds. in sub-Saharan Africa, and These children are seen every women and children are those most to be orphans, many as a result of HIV in eight weeks by Dr Ung Vibol, head of HIV affected. Despite an increasing number of their parents at National Pediatric Hospital who came to treatment programs and decreasing TSF's efforts are only a drop in Brown University a few years ago for a HIV numbers of cases, ENCHADS [The this ocean of misery, but for the children we fellowship at Hasbro Children's Hospital. National Center for HIV AIDS, Dermatology care for, a very significant drop. At this The infected children have blood tests to and STDs] estimates that approximately time, 20 %, or 11, of our orphanage monitor their CD4 counts and viral load 9, 000 children in the country are infected. children are infected with HIV, all of whom every eight weeks, plus regular liver and Only about 2000 have been identified, and were infected before birth by an HIV kidney screens, paid for by TSF, as it does only 1, 100 children are said to be on infected mother. Sadly, it is culturally not come under the Clinton funding. antiretroviral medicines, which can usually acceptable for husbands to frequent the There is nothing better than to control the HIV, and allow a fairly normal sex trade in Cambodia where some 40 % watch our absolutely "normal' HIV infected existence. [figures from Ministry of Health of women are estimated to be infected. kids enjoying very normal childhoods! UNICEF USAID]. Husbands frequent this market, become Three are old enough to go to the local Furthermore, m a l n infected, and bring HIV home to their primary school [we have 7 children now in massively compounds the severity of HIV, wives, and subsequently, their infants. Roteang primary] and it is an education for as does the concurrence of other Some of our children have arrived at the the Principal and teachers, that all of our infections, such as TB. Forty five percent of Orphanage very close to death, due to lack children are completely healthy. Roteang Cambodian children are estimated to be of treatment, concurrent infections, and Orphanage has become known for its moderately or severely underweight. severe malnutrition. Our nannies take on quality of care; two more little unrelated 670, 000 children in Cambodia are thought the challenge, and it is amazing how, with boys, each 2 12 years, with HIV and We would like to send the mothers home after their stay at Owens house with a layette of essentials for their baby. Formula is already provided, but a plastic basket [ $4.80] with a baby blanket or two, and some shirts, onesies, and something long sleeved and legged would be very welcome. In addition we would need to add in Cambodia little hand covers and a cotton bonnet, as is the custom for Cambodian newborns to wear. We'd add a couple bottles too, as bottle feeding is a must [see main story] If you have any gently used new baby size clothes or blankets you don't need, please send to our "packing center " in Maine, and they'll be on their way, starting in April. PO address is TSF, PO Box 399. Woolwich, Maine, 04579, or, alternatively UPS address: TSF, 934 Arrowsic Road, Arrowsic Maine 04530. Thanks! [P S. We continue to collect, and carry each trip, clothing for all our older kids to, up to size 18, as we supply R o t orphanage, some villagers, and Kampong Speu Orphanage--so we welcome these as well, sent by one of the above methods.] and zerit.
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40 selling and promotion expenses means, subject to the limitation set forth in section 3, i ; payments for endo's efforts directly attributable to the promotion of licensed product, plus ii ; reimbursement for third party selling and promotional activities directly attributable to the promotion of licensed product, such as a third party sales force, call targeting, call reporting and other monitoring tracking costs.
MONOCYTE MACROPHAGE TRAFFICKING IN HIV DEMENTIA COMPLEX. T. Fischer-Smith1, S. Coul2, K. Rybicka1, O. Haxhistasa1, A. Adeniyi1, R. Bonwetsch2, S. Morgello3, K. Khalili1, and J. Rappaport1 * . 1Center for Neurovirology and Cancer Biology, Temple University, Philadelphia, PA. 2Drexel University College of Medicine, Philadelphia, PA. 3 Mount Sinai School of Medicine, New York, NY. Our studies investigated the mononuclear phagocyte MP ; population s ; in CNS tissues from patients with HIV encephalitis HIVE ; using markers distinguishing macrophages from microglia. Results demonstrate the perivascular macrophage as the major productive reservoir for HIV infection in the CNS. CNS invasion rather than proliferation appears to be the principal mechanism of MP accumulation in HIVE. Organ invasion of MPs in HIVE appears to be a generalized phenomenon; MP invasion outside the CNS may contribute to the long-lived reservoir of HIV infection. Furthermore, analysis of kidney specimens from patients with HIVE revealed features associated with HIV associated nephropathy. These immunohistochemical studies, together with results from viral-genetic analysis of HIV-1 V3 sequences from CNS, lymph node and bone marrow MPs, support the importance of MP activation and trafficking in the pathogenesis of HIVE. We propose that monocyte macrophage activation, invasion and accumulation are influenced by virus induced cytokine dysregulation. The potential role of macrophage colony stimulatory factor M-CSF ; will be discussed. NEUROPROTECTIVE AND ANTI-HIV ACTIVITY OF MINOCYCLINE. M.C. Zink * , P.M. Tarwater, J.E. Clements, S.A. Barber; Dept. Comparative Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, 21205. The prevalence of HIV CNS disease has not decreased despite highly active antiretroviral therapy. Current antiretroviral therapeutics are expensive, require complex dosing regimens have significant side effects, including neurotoxicity, and few cross the blood-brain barrier. We examined the ability of minocycline, an antibiotic with potent anti-inflammatory and neuroprotective properties to protect against encephalitis and neurodegeneration using a rigorous SIV macaque model of HIV CNS disease. Macaques were treated with 4 mg kg day of minocycline beginning during early asymptomatic infection and continuing until late infection. Minocycline-treated macaques had less severe encephalitis, reduced CNS expression of neuroinflammatory markers, less axonal degeneration and lower CNS virus replication than infected, untreated macaques. Further, minocycline suppressed replication of both HIV and SIV in cultured primary lymphocytes and macrophages via p38-dependent and p38-independent MAPK pathways, respectively. Minocycline is a safe, inexpensive, readily available antibiotic that should be investigated as an anti-HIV therapeutic. MOLECULAR, FUNCTIONAL AND STRUCTURAL EFFECTS OF CHRONIC SIV INFECTION IN THE CNS. Howard Fox1 * , Michael Taffe1. Steven Henriksen1, Tricia Burdo1, Peter Gaskill1, Cecilia Marcondes1, Manisha Yadav1, Ron Mervis2, and Eleanor Roberts1 1 Department of Neuropharmacology, Scripps Research Institute, La Jolla, CA 92037; 2 NeuroStructural Research Lab, Tampa, FL 33612 The cognitive and motor disorders occurring in HIV-infected individuals result in significant morbidity and mortality, and remain a serious problem even in the era of highly active antiviral therapy. Although numerous potential neurotoxic molecules have been identified, the nature of the CNS disorder has remained elusive. Using SIV-infected rhesus monkeys, we have carried out and ticlid and retrovir.
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King correctly notes that meth is treatable; he fails to note that the dropout rates for almost all forms of drug treatment other than opiate substitution therapy are high, and that treatment doesn't work for people who don't attend it.
In both studies, the combination of irinotecan 5-FU LV therapy resulted in significant improvements in objective tumor response rates, time to tumor progression, and survival when compared with 5-FU LV alone. These differences in survival were observed in spite of second-line therapy in a majority of patients on both arms, including crossover to irinotecan-containing regimens in the control arm. Patient characteristics and major efficacy results are shown in Table 2. Improvement was noted with irinotecan-based combination therapy relative to 5-FU LV when response rates and time to tumor progression were examined across the following demographic and disease-related subgroups age, gender, ethnic origin, performance status, extent of organ involvement with cancer, time from diagnosis of cancer, prior adjuvant therapy, and baseline laboratory abnormalities ; . Figures 1 and 2 illustrate the Kaplan-Meier survival curves for the comparison of irinotecan 5FU LV versus 5-FU LV in Studies 1 and 2, respectively and ticlopidine.
HIV-1 is an RNA virus or retrovirus, which targets the cell-associated immune system particularly CD4 cells ; , crucial for normal immune functioning. There is a strong relationship between viral load and the rate of CD4 decline, along with the development of clinical symptoms. The risk of opportunistic infections and other serious clinical symptoms becomes greater once immunodeficiency is established, with AIDS diagnosed according to specific clinical and immunological criteria.1 Although the period of symptom-free infection varies between individuals, in most cases there is a 10-year period until development of serious manifestations of HIV disease in the absence of antiretroviral therapy and one to two years between AIDS diagnosis and death.2 Antiretroviral drugs, which delay the progression of HIV through the inhibition of viral replication, were first approved for use in adults in 1987. In 1996, the first evidence became available showing that combinations of three or more antiretroviral drugs are considerably more effective than single or double combinations in preventing viral replication and, hence, immunological and clinical deterioration.3, 4 Subsequently, such potent combinations also called highly active antiretroviral therapy HAART ; usually containing at least two nucleoside analogue drugs combined with a protease inhibitor or a non-nucleoside reverse transcriptase ; have become the standard of care in developed countries. The rapid uptake and widespread use of HAART has meant that HIV infection has been transformed into a chronic disease in these settings, with significant improvements in AIDS-free survival and quality of life5, 6 as a result.
| Retrovir trade nameNerve biopsy specimens are characterized by marked angiocentric CD8 infiltrates and abundant expression of HIV p24 protein without vessel wall necrosis. The treatment of DILS consists primarily of standard antiretroviral therapy and or corticosteroids. Spontaneous improvement has also been reported. The neuropathy does not appear to recur.
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Can be recycled in salvage therapy although they should not be given to females who may become pregnant ; . Whereas these medications are considered the cheapest and most readily available of antiretrovirals, we caution against the addition of hydroxyurea in such salvage therapy. We observed in this randomized trial that this did not provide any further benefit and other studies have shown that it may cause harm.
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