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Calutide (Bicalutamide)

Calutide is a new nonsteroidal antiandrogen developed for use in patients with prostate cancer. The efficacy and tolerability of Calutide as monotherapy and as combination therapy for patients with advanced prostate cancer have been evaluated in randomized clinical trials. Clinical trials are currently in progress to further evaluate Calutide as monotherapy in patients with advanced stages of disease and as adjuvant or first‐line therapy in patients with early‐stage disease.

Other names for this medication:
Bicalutamide, Casodex, Bicalox, Bicalutamida, Bicusan, Bidrostat, Caluran, Calutide, Calutol, Capro, Cosudex, Imda, Lutamidal, Probic, Zolacos,

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Fastic, Oraz, Anesteloc, Dirret, Ultop, Flubiotic, Norep, Etaconil, Otrivine, Prolertus, Optilast, Omepren, Warfarin, Camelot, Oprazole, Roxidene, Shant, Topiramate, Renil, Controloc, Flamygel, Prophenatin, Omeran, Sedate, Esertia, Algix, Zevin, Areston, Cleron, Clinacin, Ozid, Mindiab,

Calutide is used with another medication (gonadotropin-releasing hormone (GnRH) agonists; such as leuprolide or goserelin) to treat metastatic prostate cancer (cancer that started in the prostate and has spread to other parts of the body). Calutide is in a class of medications called nonsteroidal antiandrogens. It works by blocking the effect of androgen (a male hormone), to stop the growth and spread of cancer cells.

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The prevention of the Jarisch-Herxheimer reaction in penicillin therapy of congenital syphilis Rad Variant HbA1c HPLC method. Of the eight peripheral blood specimens found to be PCR-positive, five showed a change of PCR from negative to positive during surgery, and liver metastases developed 11 months later in one of these five patients. A 39-year-old woman with rheumatoid arthritis developed intrapartum anaphylaxis that led to fetal demise. Senna leaf curl virus: a novel begomovirus identified in Senna occidentalis.

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In this study, a series of novel mono- and di-substituted phenoxodiol-thiosemicarbazone hybrids were synthesized via the condensation reaction between phenoxodiol with thiosemicarbazides. From a total of 258 hits, six randomized controlled animal studies were included. Interleukin-37 induces apoptosis and autophagy of SMMC-7721 cells by inhibiting phosphorylation of mTOR Both the non-SUD and the co-occurring SUD groups had high levels of psychopathology, serious impairments in functioning and moderate levels of suicidal ideation, although those with co-occurring SUD had significantly poorer levels of functioning.

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Physicochemical characterization of mineral deposits in human ligamenta flava. Organic anion transport and action of gamma-glutamyl transpeptidase in kidney linked mechanistically to renal tubular uptake of inorganic mercury. Physical characterization using thin layer chromatography and infrared spectroscopy apparently revealed the absence of drug degradation and sizeable interaction between the drug and the polymer. Human studies demonstrate that sleep impairment is a concurrent comorbidity of autism spectrum disorders (ASD), but its etiology remains largely uncertain. Despite aggressive treatment of hepatic encephalopathy, there was no clinical improvement.

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Pattern of growth of selected groups of breast-fed infants in Iowa City. From these data, we determined grey matter cerebrovascular reactivity maps which show the spatial distribution of the responses to these interventions.

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The advent of laparoscopic cholecystectomy brought a new approach with many advantages to patients for the treatment of symptomatic gallstones. Thirteen mothers had a primary infection (six type 1, seven type 2), mostly with clinical symptoms. The Ag2S-NPs remained as Ag2S, while AgNO3 exposure led to Ag0 and sulfur-associated Ag species in plant tissue. RNA interference targeting c-Jun or ATF4 eliminated arsenite-induced APE1 transcription.

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