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Alfu (Alfuzosin)
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Alfuzosin

Alfu is used for treating symptoms of benign prostatic hyperplasia (BPH) in men with an enlarged prostate. It may also be used for certain conditions. Alfu is an alpha-blocker. It works by blocking receptors in the lower urinary tract, causing smooth muscles in the bladder neck and prostate to relax. This relaxation improves urine flow and reduces the symptoms of BPH.

Other names for this medication:
Alfuzosin, Uroxatral, Alcinin, Alfu, Alfural, Alfusin, Benestan, Dalfaz, Flotral, Mittoval, Unibenestan, Urion, Xantral, Xatral,

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Alfu is used to treat the signs and symptoms of benign enlargement of the prostate (benign prostatic hyperplasia or BPH). Benign enlargement of the prostate is a problem that can occur in men as they get older. The prostate gland is located below the bladder. As the prostate gland enlarges, certain muscles in the gland may become tight and get in the way of the tube that drains urine from the bladder. This can cause problems with urinating, such as a need to urinate often, a weak stream when urinating, or a feeling of not being able to empty the bladder completely.

Alfu helps relax the muscles in the prostate and the opening of the bladder. This may help increase the flow of urine or decrease the symptoms. However, Alfu will not shrink the prostate. The prostate may continue to get larger. This may cause the symptoms to become worse over time. Therefore, even though Alfu may lessen the problems caused by enlarged prostate now, surgery may still be needed in the future.

This medicine is usually given only to men. It is not normally given to women or children.

This medicine is available only with your doctor's prescription.

This product is available in the following dosage forms:

  • Tablet, Extended Release

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Effect of radicicol infusion on the Src tyrosine kinase activity of rat hippocampus before and after training in an inhibitory avoidance task. In vivo blunt-end cloning through CRISPR/Cas9-facilitated non-homologous end-joining. The action of bone phosphatase on the esters of phosphoric acid of the blood. Miconazole, ketoconazole, and clotrimazole inhibited the activity of calmodulin-dependent cyclic nucleotide phosphodiesterase competitively versus calmodulin concentration, zolam sleeping tablets with apparent Ki values of 6, 18, and 25 microM, respectively.

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Bacterial Growth on Distant Naphthalene Diffusing through Water, Air, and Water-Saturated and Nonsaturated Porous Media. Curcumin (120 mg/kg) was given to rats with established renal injury (30 days after surgery) and continued for 30 days (days 31-60 of the study). This suggests a corresponding functional diversification of SPANX gene families in hominoids. We sought to determine whether modified baseline side effects naprosyn sr-1000 keyence perfusion thresholds calculated by integrating baseline perfusion and clinical factors better predict tissue fate and clinical outcome.

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