Zidovudine
A dideoxynucleoside compound in which the 3'-hydroxy group on the sugar moiety has been replaced by an azido group. This modification prevents the formation of phosphodiester linkages which are needed for the completion of nucleic acid chains. The compound is a potent inhibitor of HIV replication, acting as a chain-terminator of viral DNA during reverse transcription. It improves immunologic function, partially reverses the HIV-induced neurological dysfunction, and improves certain other clinical abnormalities associated with AIDS. Its principal toxic effect is dose-dependent suppression of bone marrow, resulting in anemia and leukopenia.
Anti-HIV Agents
Didanosine
A dideoxynucleoside compound in which the 3'-hydroxy group on the sugar moiety has been replaced by a hydrogen. This modification prevents the formation of phosphodiester linkages which are needed for the completion of nucleic acid chains. Didanosine is a potent inhibitor of HIV replication, acting as a chain-terminator of viral DNA by binding to reverse transcriptase; ddI is then metabolized to dideoxyadenosine triphosphate, its putative active metabolite.
Stavudine
Lamivudine
Reverse Transcriptase Inhibitors
HIV Infections
Zalcitabine
A dideoxynucleoside compound in which the 3'-hydroxy group on the sugar moiety has been replaced by a hydrogen. This modification prevents the formation of phosphodiester linkages which are needed for the completion of nucleic acid chains. The compound is a potent inhibitor of HIV replication at low concentrations, acting as a chain-terminator of viral DNA by binding to reverse transcriptase. Its principal toxic side effect is axonal degeneration resulting in peripheral neuropathy.
Infectious Disease Transmission, Vertical
HIV-1
Nevirapine
Dideoxynucleosides
Nucleosides that have two hydroxy groups removed from the sugar moiety. The majority of these compounds have broad-spectrum antiretroviral activity due to their action as antimetabolites. The nucleosides are phosphorylated intracellularly to their 5'-triphosphates and act as chain-terminating inhibitors of viral reverse transcription.
AIDS-Related Complex
A prodromal phase of infection with the human immunodeficiency virus (HIV). Laboratory criteria separating AIDS-related complex (ARC) from AIDS include elevated or hyperactive B-cell humoral immune responses, compared to depressed or normal antibody reactivity in AIDS; follicular or mixed hyperplasia in ARC lymph nodes, leading to lymphocyte degeneration and depletion more typical of AIDS; evolving succession of histopathological lesions such as localization of Kaposi's sarcoma, signaling the transition to the full-blown AIDS.
Acquired Immunodeficiency Syndrome
An acquired defect of cellular immunity associated with infection by the human immunodeficiency virus (HIV), a CD4-positive T-lymphocyte count under 200 cells/microliter or less than 14% of total lymphocytes, and increased susceptibility to opportunistic infections and malignant neoplasms. Clinical manifestations also include emaciation (wasting) and dementia. These elements reflect criteria for AIDS as defined by the CDC in 1993.
Drug Therapy, Combination
HIV Reverse Transcriptase
A reverse transcriptase encoded by the POL GENE of HIV. It is a heterodimer of 66 kDa and 51 kDa subunits that are derived from a common precursor protein. The heterodimer also includes an RNAse H activity (RIBONUCLEASE H, HUMAN IMMUNODEFICIENCY VIRUS) that plays an essential role the viral replication process.
Pregnancy Complications, Infectious
Indinavir
CD4 Lymphocyte Count
HIV Core Protein p24
A major core protein of the human immunodeficiency virus encoded by the HIV gag gene. HIV-seropositive individuals mount a significant immune response to p24 and thus detection of antibodies to p24 is one basis for determining HIV infection by ELISA and Western blot assays. The protein is also being investigated as a potential HIV immunogen in vaccines.
Drug Resistance, Viral
Thymine Nucleotides
Viral Load
Antiviral Agents
Agents used in the prophylaxis or therapy of VIRUS DISEASES. Some of the ways they may act include preventing viral replication by inhibiting viral DNA polymerase; binding to specific cell-surface receptors and inhibiting viral penetration or uncoating; inhibiting viral protein synthesis; or blocking late stages of virus assembly.
Organophosphonates
Drug Interactions
Antiretroviral Therapy, Highly Active
HIV Protease Inhibitors
Drug Resistance, Multiple, Viral
Drug Resistance, Microbial
Botswana
HIV
Human immunodeficiency virus. A non-taxonomic and historical term referring to any of two species, specifically HIV-1 and/or HIV-2. Prior to 1986, this was called human T-lymphotropic virus type III/lymphadenopathy-associated virus (HTLV-III/LAV). From 1986-1990, it was an official species called HIV. Since 1991, HIV was no longer considered an official species name; the two species were designated HIV-1 and HIV-2.
Nelfinavir
Pregnancy
Double-Blind Method
Lopinavir
RNA-Directed DNA Polymerase
Appetite Stimulants
Saquinavir
Half-Life
HIV Seropositivity
Drug Administration Schedule
Thymidine Monophosphate
Nucleosides
Ritonavir
Leukocyte Count
AIDS Dementia Complex
A neurologic condition associated with the ACQUIRED IMMUNODEFICIENCY SYNDROME and characterized by impaired concentration and memory, slowness of hand movements, ATAXIA, incontinence, apathy, and gait difficulties associated with HIV-1 viral infection of the central nervous system. Pathologic examination of the brain reveals white matter rarefaction, perivascular infiltrates of lymphocytes, foamy macrophages, and multinucleated giant cells. (From Adams et al., Principles of Neurology, 6th ed, pp760-1; N Engl J Med, 1995 Apr 6;332(14):934-40)
Short course antiretroviral regimens to reduce maternal transmission of HIV.(1/1569)
(+info)Modulation of the cytotoxicity of 3'-azido-3'-deoxythymidine and methotrexate after transduction of folate receptor cDNA into human cervical carcinoma: identification of a correlation between folate receptor expression and thymidine kinase activity. (2/1569)
Cervical carcinoma is an AIDS-defining illness. The expression of folate receptors (FRs) in cervical carcinoma (HeLa-IU1) cells was modulated by stable transduction of FR cDNA encapsidated in recombinant adeno-associated virus-2 in the sense and antisense orientation (sense and antisense cells, respectively). Although sense cells proliferated slower than antisense or untransduced cells in vivo and in vitro in 2% (but not 10%) FCS, [methyl-3H]thymidine incorporation into DNA was significantly increased in sense cells in 10% serum; therefore, the basis for this discrepancy was investigated. The activity of thymidine kinase (TK) was subsequently directly correlated with the extent of FR expression in single cell-derived clones of transduced cells. This elevated TK activity was not a result of recruitment of the salvage pathway based on the presence of adequate dTTP pools, normal thymidylate synthase (TS) activity, persistence of increased thymidine incorporation despite the exogenous provision of excess 5,10-methylene-tetrahydrofolate, and documentation of adequate folates in sense cells. The increase in TK activity conferred significant biological properties to sense cells (but not antisense or untransduced cells) as demonstrated by augmented phosphorylation of 3'-azido-3'-deoxythymidine (AZT) and concomitantly greater sensitivity to the cytotoxic effects of AZT. Conversely, sense cells were highly resistant to methotrexate, but this was reversed by the addition of AZT. The direct correlation of FR expression and TK activity indicates a previously unrecognized consequence of FR overexpression. (+info)Inhibition of human immunodeficiency virus type 1 replication by combination of transcription inhibitor K-12 and other antiretroviral agents in acutely and chronically infected cells. (3/1569)
8-Difluoromethoxy-1-ethyl-6-fluoro-1,4-dihydro-7-[4-(2-methoxyp hen yl)-1- piperazinyl]-4-oxoquinoline-3-carboxylic acid (K-12) has recently been identified as a potent and selective inhibitor of human immunodeficiency virus type 1 (HIV-1) transcription. In this study, we examined several combinations of K-12 and other antiretroviral agents for their inhibitory effects on HIV-1 replication in acutely and chronically infected cell cultures. Combinations of K-12 and a reverse transcriptase (RT) inhibitor, either zidovudine, lamivudine, or nevirapine, synergistically inhibited HIV-1 replication in acutely infected MT-4 cells. The combination of K-12 and the protease inhibitor nelfinavir (NFV) also synergistically inhibited HIV-1, whereas the synergism of this combination was weaker than that of the combinations with the RT inhibitors. K-12 did not enhance the cytotoxicities of RT and protease inhibitors. Synergism of the combinations was also observed in acutely infected peripheral blood mononuclear cells. The combination of K-12 and cepharanthine, a nuclear factor kappa B inhibitor, synergistically inhibited HIV-1 production in tumor necrosis factor alpha-stimulated U1 cells, a promonocytic cell line chronically infected with the virus. In contrast, additive inhibition was observed for the combination of K-12 and NFV. These results indicate that the combinations of K-12 and clinically available antiretroviral agents may have potential as chemotherapeutic modalities for the treatment of HIV-1 infection. (+info)Inhibition of nucleoside diphosphate kinase in rat liver mitochondria by added 3'-azido-3'-deoxythymidine. (4/1569)
The effect of 3'-azido-3'-deoxythymidine on nucleoside diphosphate kinase of isolated rat liver mitochondria has been studied. This is done by monitoring the increase in the rate of oxygen uptake by nucleoside diphosphate (TDP, UDP, CDP or GDP) addition to mitochondria in state 4. It is shown that 3'-azido-3'-deoxythymidine inhibits the mitochondrial nucleoside diphosphate kinase in a competitive manner, with a Ki value of about 10 microM as measured for each tested nucleoside diphosphate. It is also shown that high concentrations of GDP prevent 3'-azido-3'-deoxythymidine inhibition of the nucleoside diphosphate kinase. (+info)Suppression of replication of multidrug-resistant HIV type 1 variants by combinations of thymidylate synthase inhibitors with zidovudine or stavudine. (5/1569)
The replication of recombinant multidrug-resistant HIV-1 clones modeled on clinically derived resistant HIV-1 strains from patients receiving long-term combination therapy with zidovudine (AZT) plus 2',3'-dideoxycytidine was found to regain sensitivity to AZT and stavudine (D4T) as a consequence of a pharmacologically induced decrease in de novo dTMP synthesis. The host-cell system used was phytohemagglutinin-stimulated peripheral blood mononuclear cells; dTMP and dTTP depletion were induced by single exposures to a low level of the thymidylate synthase inhibitor 5-fluorouracil (5-FU) or its deoxynucleoside, 2'-deoxy-5-fluorouridine. The host-cell response to the latter was biphasic: a very rapid decrease in the rate of de novo dTMP formation and, consequently, in intracellular dTTP pools, followed by slower recovery in both indices over 3 to 24 h. With the additional presence of AZT or D4T, however, replication of the multidrug-resistant HIV-1 strains remained inhibited, indicating dependence of HIV DNA chain termination by AZT-5'-monophosphate or 2',3'-didehydro-2', 3'-dideoxythymidine-5'-monophosphate in these resistant strains on simultaneous inhibition of host-cell de novo synthesis of thymidine nucleotides. No effect on viability of control (uninfected) phytohemagglutinin-stimulated/peripheral blood mononuclear cells was noted on 6-day exposures to 5-FU or 2'-deoxy-5-fluorouridine alone or in combination with AZT or D4T, even at drug levels severalfold higher than those used in the viral inhibition studies. These studies may provide useful information for the potential clinical use of AZT/5-FU or D4T/5-FU combinations for the prevention or reversal of multidrug resistance associated with long-term dideoxynucleoside combination therapy. (+info)Treatment with amprenavir alone or amprenavir with zidovudine and lamivudine in adults with human immunodeficiency virus infection. AIDS Clinical Trials Group 347 Study Team. (6/1569)
Amprenavir is a human immunodeficiency virus (HIV) protease inhibitor with a favorable pharmacokinetic profile and good in vitro activity. Ninety-two lamivudine- and protease inhibitor-naive individuals with >/=50 CD4 cells/mm3 and >/=5000 HIV RNA copies/mL were assigned amprenavir (1200 mg) alone or with zidovudine (300 mg) plus lamivudine (150 mg), all given every 12 h. After a median follow-up of 88 days, the findings of a planned interim review resulted in termination of the amprenavir monotherapy arm. Among 85 subjects with confirmed plasma HIV RNA determination, 15 of 42 monotherapy versus 1 of 43 triple-therapy subjects had an HIV RNA increase above baseline or 1 log10 above nadir (P=.0001). For subjects taking triple therapy at 24 weeks, the median decrease in HIV RNA was 2.04 log10 copies/mL, and 17 (63%) of 27 evaluable subjects had <500 HIV RNA copies/mL. Treatment with amprenavir, zidovudine, and lamivudine together reduced the levels of HIV RNA significantly more than did amprenavir monotherapy. (+info)2-mercapto N-(azolyl)benzenesulfonamides. VI. Synthesis and anti-HIV activity of some new 2-mercapto-N-(1,2,4-triazol-3-yl)benzenesulfonamide derivatives containing the 1,2,4-triazole moiety fused with a variety of heteroaromatic rings. (7/1569)
A series of 2-mercapto-N-(1,2,4-triazol-3-yl)benzenesulfonamide derivatives containing the triazole moiety fused with a variety of heteroaromatic rings [XVI-XXVIII] was obtained by the reactions of 3-methylthio-1,4-2-benzodithiazine 1,1-dioxide derivatives [Ia-d] with 2-hydrazines [IIa-f]. Some of the intermediate 1,1-dioxide-1,4,2-benzodithiazin-3-ylhydrazines [III-XV] initially formed were also isolated. Preliminary screening data indicated that compounds [XVI-XIX and XXVII] were anti-HIV inactive, whereas other compounds showed a high [XXI and XXIII], fairly high [XXIII and XXVI] or moderate [XX, XXIV, XXV and XXVIII] activity. The compound [XXI] exhibited also high activity against ten selected HIV mutants. (+info)Effects of human immunodeficiency virus type 1 resistance to protease inhibitors on reverse transcriptase processing, activity, and drug sensitivity. (8/1569)
Human immunodeficiency virus type 1 (HIV-1) variants resistant to protease inhibitors often display a reduced replicative capacity as a result of an impairment of protease function. Such fitness-impaired viruses display Gag precursor maturation defects. Here, we report that some protease inhibitor-resistant viruses also display abnormalities in the processing of reverse transcriptase (RT) by the protease. In three recombinant viruses carrying resistant protease sequences from patient plasma, we observed a marked decrease in the amount of mature RT subunits and of particle-associated RT activity compared to their parental pretherapy counterparts. We investigated the possibility that a decrease in the amount of particle-associated mature RT could affect the sensitivity of the corresponding virus to RT inhibitors. We observed a twofold increase of sensitivity to zidovudine (AZT) when a virus which carried AZT mutations was processed by a resistant protease. Interestingly, the presence of AZT-resistance mutations partially rescued the replication defect associated with the mutated protease. The interplay between resistance to protease inhibitors and to RT inhibitors described here may be relevant to the therapeutic control of HIV-1 infection. (+info)Maternal viral genotypic zidovudine resistance and infrequent failure of zidovudine therapy to prevent perinatal transmission...
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Zidovudine
"Retrovir- zidovudine capsule Retrovir- zidovudine solution Retrovir- zidovudine injection, solution". DailyMed. Retrieved ... It is sold both by itself and together as lamivudine/zidovudine and abacavir/lamivudine/zidovudine. It can be used by mouth or ... Zidovudine was first described in 1964. It was approved in the United States in 1987 and was the first treatment for HIV. It is ... Zidovudine (ZDV), also known as azidothymidine (AZT), is an antiretroviral medication used to prevent and treat HIV/AIDS. It is ...
List of antiviral drugs
"Zidovudine". PubChem Public Chemical Database. NCBI. Archived from the original on October 25, 2012. Retrieved April 10, 2011. ...
Brazilian Controlled Drugs and Substances Act
ZIDOVUDINE (AZT) 1. DIODROEPIANDROSTERONE (DHEA) 2. ESTANOZOLOL 3. FLUOXIMESTERONE OR FLUOXIMETHYLTESTOSTERONE 4. MESTEROLONE 5 ...
Thymidine kinase
In zidovudine (AZT; ATC:J05AF01) the 3'-hydroxyl group has been replaced by an azido group, in stavudine (ATC: J05AF04) it has ... Sun R, Eriksson S, Wang L (November 2014). "Zidovudine induces downregulation of mitochondrial deoxynucleoside kinases: ...
Mycobacterium avium-intracellulare infection
The Zidovudine Epidemiology Study Group". Am. Rev. Respir. Dis. 146 (2): 285-9. doi:10.1164/ajrccm/146.2.285. PMID 1362634. ... Mycobacterium avium-complex infections in patients with advanced human immunodeficiency virus disease treated with zidovudine. ...
Nucleoside triphosphate
"Zidovudine Monograph for Professionals - Drugs.com". Drugs.com. Retrieved 30 November 2017. Lodish H, Berk A, Zipursky SL, ...
Discovery and development of non-nucleoside reverse-transcriptase inhibitors
This was the NRTI called zidovudine. In the late 1980s, during further development of NRTIs, the field of NNRTIs discovery ...
John G. Bartlett
"Zidovudine in Asymptomatic Human Immunodeficiency Virus Infection". New England Journal of Medicine. 322 (14): 941-949. doi: ...
Organic azide
The antiviral drug zidovudine (AZT) contains an azido group. Some organic azides are classified as highly explosive and toxic. ...
Jerome Horwitz
Zidovudine was initially developed as a treatment for cancer. Horwitz was also first to synthesize stavudine (d4T) and ... Horwitz synthesized a compound that was to become known as zidovudine (AZT) - an antiviral drug used to treat HIV patients; ...
Douglas Richman
Larder, B; Darby, G; Richman, DD (1989). "HIV with reduced sensitivity to zidovudine isolated during prolonged therapy". ...
Valproate
Zidovudine: valproate may increase zidovudine serum concentration and lead to toxicity. Although the mechanism of action of ...
Catherine Wilfert
After 1993, using zidovudine during pregnancy led to an estimated reduction of mother-to-infant transmission of HIV in the ... "Zidovudine for the Prevention of HIV Transmission from Mother to Infant". 43 (16). 29 April 1994: 285-287. {{cite journal}}: ... Years into the AIDS epidemic there had not been any medication to treat HIV infection, but when zidovudine was approved, " ... France started the clinical trial of zidovudine (AZT) in HIV-infected pregnant women otherwise known as "ACTG protocol 076". ...
HIV associated cardiomyopathy
Cardiac dysfunction in the HIV-1 transgenic mouse treated with zidovudine. Lab Invest 2000;80:187-97. Lewis W, Simpson JF, ... Cardiac mitochondrial DNA polymerase gamma is inhibited competitively and noncompetitively by phosphorylated zidovudine. Circ ... Zidovudine is an example of a nucleoside analogue and has been shown to cause: myocarditis and dilated cardiomyopathy as well ...
Concentrative nucleoside transporter
It also transports the anti-viral nucleoside analogues Zidovudine and Zalcitabine. Che M, Ortiz DF, Arias IM (Jun 1995). " ...
Lawrence Corey
Combination therapy with zidovudine and didanosine compared to zidovudine alone in HIV-1 infection. Ann Intern Med. 1993 Oct 15 ... Zidovudine in Asymptomatic Human Immunodeficiency Virus Infection - A Controlled Trial in Persons with Fewer Than 500 CD4- ... Zidovudine in Asymptomatic Human Immunodeficiency Virus Infection - A Controlled Trial in Persons with Fewer Than 500 CD4- ... Treatment of human immunodeficiency virus infection with saquinavir, zidovudine, and zalcitabine. N Engl J Med. 1996 Apr 18;334 ...
Treatment as prevention
Research in 1994 revealed how the drug zidovudine can reduce vertical transmission. The testing and treatment of HIV-positive ... "Reduction of Maternal-Infant Transmission of Human Immunodeficiency Virus Type 1 with Zidovudine Treatment". New England ...
Clarithromycin
August 1997). "Clarithromycin lowers plasma zidovudine levels in persons with human immunodeficiency virus infection". ...
South East England
AZT/Retrovir (zidovudine) was first manufactured by Wellcome in 1987 in Kent; they also introduced Zovirax (aciclovir), and the ...
Reverse-transcriptase inhibitor
Zidovudine, also called AZT, ZDV, and azidothymidine, has the trade name Retrovir. Zidovudine was the first antiretroviral drug ... A virus with Q151M alone is intermediately resistant to zidovudine (AZT), didanosine (ddI), zalcitabine (ddC), stavudine (d4T ... 1994). "Combination therapy with zidovudine and didanosine selects for drug-resistant human immunodeficiency virus type 1 ... zidovudine (AZT) and stavudine (d4T) Cytidine analogues: zalcitabine (ddC), lamivudine (3TC), and emtricitabine (FTC) Guanosine ...
Didanosine
Its FDA approval helped bring down the price of zidovudine (ZDV), the initial anti-HIV drug. [Source needed on pricing effect ... Drug resistance to didanosine does develop, though slower than to zidovudine (ZDV). The most common mutation observed in vivo ...
Organic anion transporter 1
Since stavudine and zidovudine are OAT1 substrates, they may have similar effects on proximal renal tubule cells as they do on ... Combining zidovudine with stavudine does not increase the mitochondrial toxicity compared to stavudine alone. Both of these ... Zidovudine inhibits the phosphorylation of stavudine. This might reduce the toxicity of the combination. Using indinavir in ... In vitro the antiviral drugs didanosine and zidovudine are more potent inhibitors of mitochondrial DNA synthesis than tenofovir ...
Nevirapine
A short course of maternal Lamivudine/zidovudine is recommended by the U.S. Public Health Service Task Force to reduce this ... A subsequent study in Thailand showed that prophylaxis with single-dose nevirapine in addition to zidovudine is more effective ... Guay LA, Musoke P, Fleming T (Sep 1999). "Intrapartum and neonatal single-dose nevirapine compared with zidovudine for ... Conway B, Wainberg MA, Hall D (Jul 2001). "Development of drug resistance in patients receiving combinations of zidovudine, ...
AZT (disambiguation)
AZT (azidothymidine) or zidovudine is an antiretroviral drug used to treat HIV/AIDS. AZT or azt may also refer to: Azerbaijan ...
Protide
In particular, diaryl phosphates were prepared from zidovudine (AZT) using simple phosphorochloridate chemistry. For the first ...
Discovery and development of nucleoside and nucleotide reverse-transcriptase inhibitors
The first nucleoside reverse-transcriptase inhibitor with in vitro anti-HIV activity was zidovudine. Since zidovudine was ... However, zidovudine is relatively toxic since it is converted into the triphosphate by the cellular enzymes and therefore it is ... In 1964 zidovudine (AZT) was synthesized by Horwitz at the Michigan Cancer Foundation. The 3´hydroxyl group in the deoxyribose ... In 1974 zidovudine was reported to have activity against retroviruses and was subsequently re-screened as an antiviral when the ...
Lamivudine
... /zidovudine (with zidovudine) Abacavir/lamivudine (with abacavir) Abacavir/lamivudine/zidovudine (with zidovudine and ... Do not prescribe lamivudine/zidovudine, abacavir/lamivudine, or abacavir/lamivudine/zidovudine to patients taking emtricitabine ... Lamivudine was approved by the Food and Drug Administration (FDA) on November 17, 1995, for use with zidovudine (AZT) and again ... Lamivudine is often given in combination with zidovudine, with which it is highly synergistic. Lamivudine treatment has been ...
Ribavirin
Alvarez D, Dieterich DT, Brau N, Moorehead L, Ball L, Sulkowski MS (October 2006). "Zidovudine use but not weight-based ... Ribavirin should not be given with zidovudine because of the increased risk of anemia; concurrent use with didanosine should ...
Declaration of Helsinki
Critics claimed that the Zidovudine trials in developing countries were in breach of this because Zidovudine was now the best ... This was a placebo controlled trial which showed a reduction of nearly 70% in the risk of transmission, and Zidovudine became a ... The AIDS Clinical Trials Group (ACTG) Study 076 of 100 Zidovudine in maternal-infant transmission of HIV had been published in ... "Reduction of Maternal-Infant Transmission of Human Immunodeficiency Virus Type 1 with Zidovudine Treatment". New England ...
List of Wayne State University people
Zidovudine; synthesized Zalcitabine (ddC) and Stavudine (d4T), the third and fourth drugs approved to treat AIDS Adrian ...
Zidovudine: MedlinePlus Drug Information
Zidovudine: learn about side effects, dosage, special precautions, and more on MedlinePlus ... Zidovudine is given to HIV-positive pregnant women to reduce the chance of passing the infection to the baby. Zidovudine is in ... Zidovudine controls HIV infection but does not cure it. Continue to take zidovudine even if you feel well. Do not stop taking ... Before taking zidovudine,. *tell your doctor and pharmacist if you are allergic to zidovudine, any other medications, or any of ...
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Birth Outcomes Following Zidovudine Therapy in Pregnant Women
... Approximately 100,000 childbearing-aged women in the United ... Zidovudine for the prevention of HIV transmission from mother to infant. MMWR 1994;43:285-7. ... In January 1989, the Zidovudine in Pregnancy Registry was established by the Wellcome Foundation, in conjunction with CDC, and ... In January 1993, the Zidovudine in Pregnancy Registry was expanded to include zalcitabine and became the Antiretroviral ...
Occupational exposure (HIV) include zidovudine postexposure use
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What do we know about the potential effects of in-utero zidovudine exposure? Is it safe to use during pregnancy? ... Objective: Zidovudine (ZDV) has been extensively used in pregnant women to prevent vertical transmission of HIV but few studies ... Zidovudine (ZDV) was the first approved antiretroviral medication used for preventing the transmission of HIV from mother to ... Table 2. Multivariable associations of the number of whole-exome detected clonal SNVs and indels with zidovudine exposure and ...
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keywords = "Macacca mulatta, Zidovudine, pharmacokinetics, zidovudine-glucuronide",. author = "Ridgway, {Louis E.} and King, { ... Placental Transport of Zidovudine in the Rhesus Monkey. Louis E. Ridgway, Thomas S King, George I. Henderson, Steven Schenker, ... Placental Transport of Zidovudine in the Rhesus Monkey. / Ridgway, Louis E.; King, Thomas S; Henderson, George I. et al. ... Placental Transport of Zidovudine in the Rhesus Monkey. In: Infectious diseases in obstetrics and gynecology. 1993 ; Vol. 1, No ...
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300mg1
- Duovir tablets contain a combination the active ingredients lamivudine (150mg) and zidovudine (300mg), which are antiretroviral drugs that are used to treat HIV infection. (inhousepharmacy.vu)
Lamivudine and zidovudine11
- Dose adjustment may be necessary, separate preparations of abacavir, lamivudine and zidovudine should be administered. (mims.com)
- Abacavir, lamivudine and zidovudine are all nucleoside reverse transcriptase inhibitors. (mims.com)
- approx 1 hr (lamivudine and zidovudine). (mims.com)
- lamivudine and zidovudine also cross the placenta and are distributed into breast milk. (mims.com)
- Abacavir, lamivudine and zidovudine are metabolised by intracellular kinase to carbovir triphosphate (active triphosphate form of abacavir), lamivudine triphosphate and zidovudine triphosphate, respectively. (mims.com)
- PAXLOVID consists of 2 medicines: nirmatrelvir and ritonavir.Do not stop taking lamivudine and zidovudine without talking to your doctor.The client asks why she has to take both medications, which explanation should the nurse provide?Patient Drug Interactions Source: RxList People with HIV should start taking HIV medicines as soon as possible.CORRECT: Vomiting and other GI effects are adverse effects of zidovudine. (natuurlijke-hoeven.nl)
- Duovir contains a combination of 2 antiretroviral drugs, lamivudine and zidovudine, that are used to treat HIV infection. (inhousepharmacy.vu)
- Duovir tablets contain a combination of two antiretroviral drugs lamivudine and zidovudine, which both belong to class of drugs known as nucleoside analogue reverse transcriptase inhibitors (NRTI) that are only effective against retroviruses (RNA virus) like HIV. (inhousepharmacy.vu)
- A nucleoside is a building block of DNA that is needed by the virus to replicate, and nucleoside analogues, like lamivudine and zidovudine in Duovir tablets, become incorporated into the DNA that is copied from the virus RNA by an enzyme called reverse transcriptase. (inhousepharmacy.vu)
- Duovir tablets contain a combination of two antiretroviral drugs lamivudine and zidovudine which are used to treat HIV infection in patients with or without acquired immunodeficiency syndrome or AIDS. (inhousepharmacy.vu)
- Lamivudine and zidovudine in Duovir tablets are inhibitors of the enzyme reverse transcriptase which is needed by retroviruses (RNA viruses) like HIV to become incorporated into the DNA of infected immune cells so that they can replicate. (inhousepharmacy.vu)
Retrovir3
- Additionally, some physicians and some institutions have offered the option of using zidovudine (azidothymidine, AZT, ZDV, Retrovir) after occupational exposure to HIV (6). (cdc.gov)
- Zidovudine (retrovir, retrovir) 100 mg, single packs come in 50 mg and 100 mg doses and have the same prescription coverage as pills you get in a bottle. (nephew.dk)
- Those who are zidovudine cost Retrovir by their doctors may be able to obtain their medicine through Prescription Hope for an affordable price. (nephew.dk)
Tablets4
- Lamivudine is highly synergistic with zidovudine, which means that it increases the effectiveness of zidovudine so that the combination of these two antiretroviral drugs in Duovir tablets slow down the replication of HIV within your body but cannot prevent the spread of the infection to others. (inhousepharmacy.vu)
- Last Many Year Fonity Pharmacerutival Provided Lamivudine Zidovudine & Nevirapine Tablets is used as antiretroviral combination therapy for the treatment of HIV infection. (fonitypharmaceutical.com)
- Abacavir, zidovudine, or stavudine as paediatric tablets for African HIV-infected children (CHAPAS-3): an open-label, parallel-group, randomised controlled trial. (ox.ac.uk)
- We aimed to compare stavudine, zidovudine, or abacavir as dual or triple fixed-dose-combination paediatric tablets with lamivudine and nevirapine or efavirenz. (ox.ac.uk)
Combivir1
- Chiropraxes ordering lamivudine zidovudine uk online snagging housewrecker but pockiest combivir cheap no rx required canada korea nucleospindle above an dressier. (astergastrocare.com)
Tablet1
- Zidovudine comes as a capsule, tablet, and syrup to take by mouth. (medlineplus.gov)
Take zidovudine3
- Infants 6 weeks of age and younger may take zidovudine every 6 hours. (medlineplus.gov)
- Take zidovudine exactly as directed. (medlineplus.gov)
- Continue to take zidovudine even if you feel well. (medlineplus.gov)
Antiretroviral6
- In January 1993, the Zidovudine in Pregnancy Registry was expanded to include zalcitabine and became the Antiretroviral Pregnancy Registry. (cdc.gov)
- Lamivudine/zidovudine is indicated as part of antiretroviral combination therapy for the treatment of human immunodeficiency virus (HIV) infected adults and children. (europa.eu)
- Zidovudine (ZDV) was the first approved antiretroviral medication used for preventing the transmission of HIV from mother to child. (medscape.com)
- Zidovudine is an antiretroviral agent, prescribed for HIV/AIDS. (medindia.net)
- IMSEAR at SEARO: "Buffalo Hump" in a Female on Zidovudine-Based Antiretroviral Therapy: A Case Report. (who.int)
- Agrawal P, Gautam A, Chandra S, Aneez A, Gupta A. "Buffalo Hump" in a Female on Zidovudine-Based Antiretroviral Therapy: A Case Report. (who.int)
Infection9
- Zidovudine is used along with other medications to treat human immunodeficiency virus (HIV) infection. (medlineplus.gov)
- Zidovudine is given to HIV-positive pregnant women to reduce the chance of passing the infection to the baby. (medlineplus.gov)
- Zidovudine controls HIV infection but does not cure it. (medlineplus.gov)
- Zidovudine is also used along with other medications in certain situations to treat healthcare workers and other individuals exposed to HIV infection after accidental contact with HIV-contaminated blood, tissues, or other body fluids. (medlineplus.gov)
- This report reviews Public Health Service (PHS) recommendations for postexposure management of workers who have occupational exposures that may place them at risk of acquiring HIV infection, provides background information on zidovudine and experience with zidovudine postexposure prophylaxis, and presents considerations relevant to a decision to offer postexposure prophylaxis. (cdc.gov)
- Zidovudine, didanosine, and zalcitabine in the treatment of HIV infection: meta-analyses of the randomised evidence. (ox.ac.uk)
- get as few as 120 courses of treatment at first Then you'd get yelled at why take ritonavir and zidovudine together by people who don't understand technology or why you didn't predict one of the 1 million things that could go wrong.The combination of lopinavir and ritonavir is used with other medications to treat human immunodeficiency virus (HIV) infection. (natuurlijke-hoeven.nl)
- Zidovudine treats HIV infection. (medicap.com)
- Zidovudine is a prescription medication used to treat human immunodeficiency virus (HIV) infection. (medicap.com)
Pregnant women5
- When zidovudine is taken by pregnant women, it may be taken 5 times a day. (medlineplus.gov)
- Objectives: To respond to the primary safety objective of the Perinatal HIV Prevention Trial 1 (PHPT-1) by studying the evolution of haematological parameters according to zidovudine exposure duration in HIV-1−infected pregnant women. (harvard.edu)
- Setting: 27 hospitals in Thailand.Participants: 1,436 HIV-infected pregnant women in PHPT-1.Intervention: Zidovudine prophylaxis initiation at 28 or 35 wk gestation. (harvard.edu)
- Zidovudine (ZDV) has been extensively used in pregnant women to prevent vertical transmission of HIV but few studies have evaluated potential mutagenic effects of ZDV during fetal development. (medscape.com)
- Prenatal and postpartum zidovudine adherence among pregnant women with HIV. (bvsalud.org)
Abacavir2
- Each tab contains abacavir 300 mg, lamivudine 150 mg and zidovudine 300 mg: 1 tab bid. (mims.com)
- After two were excluded due to randomisation error, 156 children were analysed in the stavudine group, 158 in the zidovudine group, and 164 in the abacavir group, and followed for median 2·3 years (5% lost to follow-up). (ox.ac.uk)
AIDS4
- Although zidovudine does not cure HIV, it may decrease your chance of developing acquired immunodeficiency syndrome (AIDS) and HIV-related illnesses such as serious infections or cancer. (medlineplus.gov)
- METHODS: Individual patient data were available for 7722 participants without AIDS in the nine randomised trials of immediate versus deferred zidovudine, and 7700 participants with or without AIDS in the six trials comparing zidovudine plus didanosine, zidovudine plus zalcitabine, or zidovudine alone. (ox.ac.uk)
- Zidovudine (ZDV) and clarithromycin (CLR) are often used simultaneously in the management of patients with AIDS. (uri.edu)
- Effect of zidovudine resistance mutations on virologic response to treatment with zidovudine-lamivudine-ritonavir: genotypic analysis of human immunodeficiency virus type 1 isolates from AIDS clinical trials group protocol 315.ACTG Protocol 315 Team. (rush.edu)
Medications3
- Zidovudine is in a class of medications called nucleoside reverse transcriptase inhibitors (NRTIs). (medlineplus.gov)
- tell your doctor and pharmacist if you are allergic to zidovudine, any other medications, or any of the other ingredients in zidovudine products. (medlineplus.gov)
- these costs zidovudine cost often higher for branded medications than for generic medications. (nephew.dk)
Pregnancy2
- In January 1989, the Zidovudine in Pregnancy Registry was established by the Wellcome Foundation, in conjunction with CDC, and has been managed by the Burroughs Wellcome Co. (Research Triangle Park, North Carolina), * the manufacturer of ZDV. (cdc.gov)
- This result provides reassurance about the safety of early initiation of zidovudine prophylaxis during pregnancy to maximize prevention of perinatal HIV. (harvard.edu)
Adherence1
- To the extent that pill burden, rather than drug frequency, results in reduced adherence, generic Zidovudine cost could lead to decreased costs but at the potential expense of worsening virologic suppression rates and poorer clinical outcomes. (nephew.dk)
Zalcitabine5
- BACKGROUND: To assess the effects of zidovudine, didanosine, and zalcitabine on HIV disease progression and survival, we undertook meta-analyses of individual patient data and tabular data from all randomised trials that compared these agents. (ox.ac.uk)
- In the comparison of zidovudine plus didanosine or zalcitabine versus zidovudine alone, during a median follow-up of 29 months, 2904 individuals progressed, of whom 1850 died. (ox.ac.uk)
- Similarly, the addition of zalcitabine to zidovudine also delayed progression (0.86 [0.78-0.94], p=0.001) and death (0.87 [0.77-0.98], p=0.02). (ox.ac.uk)
- Five of the six trials involved randomised comparisons of zidovudine plus didanosine versus zidovudine plus zalcitabine: in these, the zidovudine plus didanosine regimen had greater effects on disease progression (p=0.004) and death (p=0.009). (ox.ac.uk)
- However, the use of didanosine and, to a lesser extent, zalcitabine delayed both disease progression and death, at least when added to zidovudine. (ox.ac.uk)
Generic3
- Generic manufacturer for IV zidovudine (Pharmaforce Inc. (hopkinsguides.com)
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Efficacy3
- We specifically considered the impact of the different resistance patterns generated by the use of TDF or ZDV in first-line cART on efficacy zidovudine cost second-line therapy and subsequent morbidity and mortality. (nephew.dk)
- An epidemiologic study was initiated in 1987 to evaluate the long-term safety and efficacy of zidovudine in patients with advanced human immunodeficiency virus disease. (elsevier.com)
- Zidovudine Epidemiology Study Group 1991, ' Long-term Safety and Efficacy of Zidovudine in Patients With Advanced Human Immunodeficiency Virus Disease ', Archives of internal medicine , vol. 151, no. 5, pp. 981-986. (elsevier.com)
Metabolism1
- Human inter-individual variability in metabolism and genotoxic response to zidovudine. (cdc.gov)
Versus2
- The evolution of haematological parameters was estimated between 26 and 35 wk (zidovudine/placebo) and between 35 wk and delivery to compare a long versus short zidovudine exposure. (harvard.edu)
- FINDINGS: In the comparison of immediate versus deferred zidovudine, during a median follow-up of 50 months, 1908 individuals progressed, of whom 1351 died. (ox.ac.uk)
Regimen2
- Data collected in an ongoing CDC surveillance project of health-care workers who have been occupationally exposed to blood from HIV-infected patients (7) indicate that during the period April-December 1989, 13 (8.6%) of 151 newly enrolled participants began a postexposure regimen of zidovudine. (cdc.gov)
- Zidovudine cost the present simulations, we aimed to re-assess the cost effectiveness of TDF over ZDV for settings using the public health approach for ART with one standard first-line and one standard second-line regimen, and without virological monitoring, which is the reality in most resource-poor settings. (nephew.dk)
Treatment5
- Results from a recent multicenter randomized double-blind clinical trial suggest that treatment of HIV-positive mothers and their infants with zidovudine (ZDV) may substantially reduce the risk for perinatal HIV transmission (3). (cdc.gov)
- Zidovudine patients should be stable on alpha-blocker therapy prior to initiating treatment and should be initiated at 25 mg. (nephew.dk)
- Table 17 includes three benchmark prices, rounded to the nearest dollar, for commonly used zidovudine cost ARV drugsa as a general reference for health care providers when considering the cost of HIV treatment. (nephew.dk)
- At delivery, the differences were not statistically significant, except for mean haemoglobin level, which remained slightly lower in the long zidovudine treatment group (difference: 0.2 g/dl). (harvard.edu)
- Reduction of maternal-infant transmission of human immunodeficiency virus type 1 with zidovudine treatment. (phosphorylaseinhibitors.com)
Damage to the liver2
- Zidovudine also may cause life-threatening damage to the liver and a potentially life-threatening condition called lactic acidosis (buildup of lactic acid in the blood). (medlineplus.gov)
- Zidovudine can cause serious damage to the liver and a condition called lactic acidosis. (medicap.com)
Pharmaceuticals1
- Zidovudine is intended for Pharmaceuticals applications. (alsachim.com)
Abstract1
- abstract = "Objective: This study was undertaken to characterize the pharmacokinetics of zidovudine (ZDV) and ZDV-glucuronide (ZDVG) in the material and fetal circulations of the rhesus monkey. (uthscsa.edu)
Doses1
- If you miss doses or stop taking zidovudine, your condition may become more difficult to treat. (medlineplus.gov)
Composition1
- Zidolam contains Zidovudine and Lamivudine as composition. (heterohealthcare.com)
Https1
- To click a baga, https://www.astergastrocare.com/doctors/buy-cheap-lamivudine-zidovudine-buy-safely-online-tennessee/ everyone rehem reconsolidating the airbubble prior to fleshier backstair. (astergastrocare.com)
Prevention1
- Intrapartum and neonatal single-dose nevirapine compared with zidovudine for prevention of mother-to-child transmission of HIV-1 in Kampala, Uganda:18 month follow-up of the HIVNET 012 randomised trial. (phosphorylaseinhibitors.com)
Time2
- Zidovudine may cause muscle disease, especially when taken for a longer period of time. (medlineplus.gov)
- Receiving zidovudine for a high proportion of time significantly improved chances of survival even if anemia developed. (elsevier.com)
Response1
- Your doctor will order certain lab tests to check your response to zidovudine. (medlineplus.gov)
Price3
- As featured and zidovudine cost in: This federally established price is the federal upper limit FUL ‒ where can i buy tadalafil online . (nephew.dk)
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