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Uromax (Oxybutynin)

Uromax is an oral drug that is used for treating urinary bladder spasm. Uromax has a dual mechanism of action. Contraction of the smooth muscle of the bladder is stimulated by the release of acetylcholine by the nerves within the bladder and the attachment of the acetylcholine to receptors on the surface of the bladder's muscle cells. Uromax suppresses involuntary contractions of the bladder's smooth muscle (spasms) by blocking the release of acetylcholine. This is referred to as an "anticholinergic effect." Uromax also directly relaxes the bladder's outer layer of muscle (the detrusor muscle). The FDA approved Uromax in July 1975.

Other names for this medication:
Oxybutynin, Oxytrol, Delak, Dresplan, Gelnique, Kentera, Lenditro, Lyrinel, Novitropan, Oxybutynine, Uricont, Uromax, Uroxal,

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Ometac, Azen, Emifenac, Fincar, Zolsoma, Alpam, Acuren, Urion, Zolpidem, Istin, Levedad, Kripton, Orten, Belmazol, Zolpi, Lertus, Clopivas, Virustat, Visram, Cobese, Isordil, Lopo, Bactelan, Zymycin, Esmolol, Dicorate, Dolotram, Lodipine, Danovir, Anzitor, Epratenz, Ziprasidone, Suftrex, Opam, Cyclophosphamide, Belivon, Poxet, Gastromax, Hascovir, Segan, Nacor,

This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

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In two different xenograft models on the basis of the canine soft tissue sarcoma STSA-1 and the prostate carcinoma DT08/40 cell lines, a systemic administration of the LIVP6.1.1 virus was found to be safe and led to anti-tumor and immunological effects resulting in the significant reduction of tumor growth in comparison to untreated control mice. The peak torques at various angular velocities (30, 60, 120, and 180 degrees/s) indicated statistically significant positive correlations to the percent number and area of FTa fibers in m. The PC-PART may have sufficient interrater reliability and clinical utility to evaluate program outcomes. The cardioacceleratory peptide CAP(2b) of the urispas flavoxate hcl 100mg hawkmoth Manduca sexta shares close amino acid identity with the PVKs and may thus be included as a structural member of the PVK peptide family.

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