Clovir is a substance used to prevent or treat cytomegalovirus and herpes simplex infections that may occur when the body is immunosuppressed. It belongs to the family of drugs called antivirals. It works by decreasing the production of the virus's DNA.Clovir was patented in 1974, and approved for medical use in 1981. It is on the World Health Organization's List of Essential Medicines, the safest and most effective medicines needed in a health system. It is available as a generic medication and is marketed under many brand names worldwide.
Other names for this medication:
Acyclovir,
Abduce,
Acic,
Aciclobeta,
Aciclomed,
Aciclostad,
Aciclovirum,
Acifar,
Acihexal,
Aciklovir,
Acitop,
Acivir,
Acivirex,
Acivision,
Acix,
Actios,
Activir,
Acycloguanosine,
Acyl,
Acyrax,
Acyvir,
Aklovir,
Antivir,
Asiviral,
Avir,
Aviral,
Avix,
Avorax,
Blistex,
Cicloferon,
Cicloviral,
Clinovir,
Clirbest,
Clopes,
Clovate,
Clovir,
Cusiviral,
Cyclomed,
Cyclovax,
Cyclovex,
Cyclovir,
Danovir,
Declovir,
Epsin,
Eurovir,
Hascovir,
Hernovir,
Herperax,
Herpesil,
Herpesin,
Herpex,
Herpin,
Herplex,
Heviran,
Immunovir,
Lisovyr,
Lovir,
Lovire,
Lovrak,
Medovir,
Menova,
Ocuvir,
Poviral,
Ranvir,
Remex,
Rexan,
Scanovir,
Sitavig,
Sophivir,
Soviclor,
Supraviran,
Telviran,
Uniplex,
Vilerm,
Viraban,
Viralex,
Viratac,
Viratop,
Virest,
Virestat,
Virex,
Virless,
Virolex,
Viromed,
Virosil,
Virostatic,
Virovir,
Virucid,
Viruderm,
Virustat,
Virux,
Vivorax,
Xiclovir,
Xorox,
Zevin,
Ziverone,
Zoral,
Zorax,
Zoraxin,
Zovirax,
Similar Products:
Lyrinel,
Clarithromycin,
Fenered,
Sanprima,
Metco,
Naxy,
Bamalite,
Setinin,
Dapoxetina,
Maclar,
Seclo,
Benolaxe,
Syneclav,
Gabatine,
Capro,
Germentin,
Venlaxor,
Tavex,
Esoprax,
Letop,
Esomeprazole,
Tryptanol,
Terbinafine,
Yucomy,
Ivermectin,
Westoxetin,
Ledifos,
Quantrum,
Antirobe,
Sutrim,
Eliwel,
Vagimid,
Levomac,
Janacin,
Mectizan,
Ulcratex,
Clomipramina,
Klamoxyl,
Amitrip,
Clopidogrel,
Blugat,
Ombitasvir,
Diflazon,
Depramine,
Incidentally detection of non-palpable testicular nodules at scrotal ultrasound: what is new? Here we present the synthesis, pharmacological activity, and molecular docking of novel non-competitive antagonists of GluK2 receptor. Retraction of: Statin enhances cytokine-mediated induction of nitric oxide synthesis in vascular smooth muscle cells. The present study shows that proximal tibial lengthening by DO in CPT can be safely performed if the proximal tibia is not dysplastic and unevaluated withdrawal from effexor has not been lengthened previously and that lengthening at a dysplastic proximal tibial segment or at a previously lengthened segment renders delayed healing and may require additional procedure(s) to promote bone healing. On July 1st 2008, community skin cancer screening (cSCS) was established in routine care of the German statutory health insurances (SHI).
Further epidemiological studies are required to map the distribution glamin drug of P. Multiple regression analysis was carried out for statistical significance of the clinical and demographic variables.
Cardiopulmonary receptor deactivation and stimulation also induced clear-cut changes in plasma renin activity in hypertensive subjects, but the percent magnitude of the reflex plasma renin activity excursion was less than that in normotensive subjects. Genetic analyses in Saccharomyces cerevisiae demonstrate that ASF1 is essential for normal cell cycle progression, and suggest that olexin 20 mg RCAF mediates chromatin assembly after DNA replication and the repair of double-strand DNA damage in vivo.
In order to monitor trends in illicit drug use among youth, surveillance of drug use behaviours among a variety of populations in different settings is required. There have been many reports that favor aggressive systemic treatment with chemotherapy and radiotherapy, even for well-localized lymphomas, avoiding the need for tonsillectomy of the normal tonsil. The estimated adult dietary intakes of PCDD/Fs and PCBs arising from the consumption of a typical portion of these foods in combination with an otherwise average UK diet were in the range 0.5-0.6 pg World Health Organisation (WHO)-toxic equivalent (TEQ)(2005)/kg bodyweight per day. There was reasonable agreement between relevant parts of the questionnaire and frequency-volume charts when a relatively flexible approach was taken, but there nebenwirkungen kepinol forte singing was a very poor relationship between questions assessing strength of stream and the results of uroflowmetry. Limited services interim methadone maintenance can reduce heroin use among persons awaiting entry into comprehensive treatment and increase the percentage entering treatment.
The consensus sequence d(AGAGGTGGGCAGGTGG)6.5 is shown to stimulate homologous recombination up to 13.5-fold. One of the main challenges to industrial application of the lignocellulosic conversion process is the high costs of cellulolytic enzymes. Smoking-related diseases--the role of physician (pathologist) in diagnosis and preventive activities A reduction ziagen and alcohol in EPS production increased bacterial adhesion to chicken gut explants, but made the bacteria less able to survive some stresses.
Comparison of the lipid-lowering effects of four different n-3 highly unsaturated augmentin 1g uses fatty acids in HepG2 cells. Compared to unpotentiated tissue, there was a significant increase in the concentration of free arachidonic acid 2.5 min, 45 min and 3 h after induction of long-term potentiation. Lonidamine induces apoptosis in drug-resistant cells independently of the p53 gene.
Tracings were produced from frontal radiographs of 11 anencephalic foetuses. Cosegregation of E397X mutation and tibotec prezista manufacturer LDLR gene RFLP haplotypes with hyperlipidemia was demonstrated by family study.
Furthermore, using an in vitro kinase assay, we show that LARG can be directly phosphorylated by Cdk1. Human neutrophils produce high levels of the interleukin 1 receptor antagonist in response to telaprevir hiv treatment granulocyte/macrophage colony-stimulating factor and tumor necrosis factor alpha. X-ray wavefront characterization using a rotating shearing interferometer technique.
Solid-phase polymerase chain reaction: applications for direct detection of enteric pathogens in waters. Structural studies of (N-phenylthioureidoalkyl- and -aryl)phosphonates. Kiil and coil dialysers proved equally satisfactory from a medical standpoint and equally acceptable to the patients. In the light-dark exploration test, tg mice made more exits, spent significantly more time on a well-lit elevated bar and went farther away from the dark box as compared to metronidazole-resistant trichomoniasis treatment with flagyl wt mice. The prediction of electronic spectra for photosensitizer molecules can be a valuable tool in the design of drugs for application in PDT.
jejuni in urban wild birds and pets and its temporal trend in the Manawatu region of New Zealand. In this case of AML-M0, increased numbers of maturing and mature bone marrow granulocytic cells staining simultaneously nilutamide flutamida y bicalutamide medication for both specific and non-specific esterase (double esterase) are described. This study focuses on the diagnostics of two natural enemy species, belonging to the genus Phytoseiulus in the family Phytoseiidae (sub-family Amblyseiinae): P. Tat treatment of neuronal cultures enhanced phosphorylation of NR2A Y1325, indicating that this site is tat sensitive.
Characterization of the distribution, polymorphism, and stability of nimodipine in its solid dispersions in polyethylene glycol by micro-Raman spectroscopy and venlafaxine hcl er cap 75mg powder X-ray diffraction. Mutational inactivation in cancer of key apoptotic pathway components, such as TP53/p53, undermines cytotoxic therapies that aim to increase apoptosis. Blockade of P/Q-type (CaV2.1) channels slightly decreased responses to chemical and cold stimuli but markedly increased spontaneous activity, an effect which was absent during concomitant application of GABA to the brainstem.
Helping this population presents a major challenge to health professionals. Hepatitis pansec dosage calculator C virus NS3 protease inhibitors comprising a novel aromatic P1 moiety.