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Urimax (Tamsulosin)
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Tamsulosin

Urimax is an oral drug for the treatment of men who are having difficulty urinating because of enlarged prostates from benign prostatic hyperplasia (BPH). Urimax is not prescribed for women. This medication is used only in men. It is not known if Urimax is secreted into human milk. Urimax was approved by the FDA in 1997. Urimax is usually taken once a day, approximately 30 minutes after a meal. Try to take Urimax at the same time each day. Do not crush, chew, or open a Urimax capsule.

Other names for this medication:
Tamsulosin, Flomax, Asoflon, Bazetham, Contiflo, Espontal, Flomaxtra, Fokusin, Gotely, Harnal, Harnalidge, Hartam, Lostam, Lura, Maxrin, Mecir, Omexel, Omic, Omix, Omnexel, Omnic, Omsal, Pradif, Prostacure, Proximic, Ranomax, Restream, Sebrane, Secotex, Stronazon, Tabphyn, Tadin, Tamik, Tamnic, Tamsin, Tamsol, Tamsudil, Tamsul, Tamsulosina, Tamsulosine, Uprox, Urimax, Urolosin,

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Clearance from apical medium to cells (CL12), cells to apical medium (CL21), cells to basolateral medium (CL23) and basolateral medium to cells (CL32) were calculated based on a three compartment model. This study provides the first evidence of an alteration in matrix degradation in haemochromatosis that may be a contributing factor to hepatic fibrogenesis in this disease. Presence of leukocytes in crevices of healthy and chronically inflamed gingivae. Natural ventilation reduces high TB transmission risk in traditional homes in rural KwaZulu-Natal, South Africa. In the presence of elevated levels of glucose similar to those seen in poorly controlled diabetics (20 mM above control), there is inhibition of neurite growth, reduction in neurite caliber, beading of neurites, and retraction of the neurite growth cone.

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The delta-aminolevulinic acid synthetase activity and the effect of exogenous delta-aminolevulinate on the synthesis of cytochrome c in the thoracic muscles of the tobacco horn worm during adult development. Leukopenia-inducing effect of a combination of a new 5-fluorouracil (5-FU)-derived drug, BOF-A2 (emitefur), with other 5-FU-derived drugs or BV-araU (sorivudine) in rats. Both selenium deficiency and toxicity are serious problems worldwide. Preeclampsia is compared by the the insufficient trofoblastic invasion to the maternal spiral arteries. The premature C2 ovulation occurs 6-7 h after the administration of progesterone (P4) injected 14 h before the spontaneous second (C2) ovulation of a sequence and therefore 7-8 h earlier than expected, (c) the ME in vitro release of beta END in both models, and (d) the effect of beta END and naloxone on in vitro ME-LHRH release in the two models.

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