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Alfuzosin

Alfuzosin is used to treat benign prostatic hyperplasia (BPH) in men. This is a condition that causes you to have an enlarged prostate. This medicine relaxes the muscles in the prostate and the bladder which reduces symptoms and improves urine flow. This medicine is not for use in women.

Other names for this medication:
Alfdo, Alfoo, Alfuprost, Alfusin, Alfuzin, Alfuzosin, Dutalfa, Flotral, Profuzo, Xelflo

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Description

Generic Alfuzosin 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. Generic name of Generic Alfuzosin is Alfuzosin. Brand name of Generic Alfuzosin is Alfuzosin.

Dosage

Usual Adult Dose for Benign Prostatic Hyperplasia:

Extended-release tablet: 10 mg orally once a day immediately after the same meal each day

Detailed Alfuzosin dosage information

Overdose

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

Storage

Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F) away from moisture, light and heat. Throw away any unused medicine after the expiration date. Keep out of the reach of children in a container that small children cannot open.

Side effects

The most common side effects associated with Alfuzosin are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.

Contraindications

Avoid driving or hazardous activity until you know how this medicine will affect you. Your reactions could be impaired.

Drinking alcohol with this medicine can cause side effects.

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Diagnosing diabetes with A1C: implications and considerations for measurement and surrogate markers. The most frequent infection localization was skin and soft tissues followed by urinary tract infection. Paying physicians according to their resource-costs: the development of a resource-based relative value scale. Spanning the distance and resource gaps in health promotion and health education programs. Genetical and biochemical evidence suggests that Nik1 interacts with the Cdc28 complex. Enteral nutrition (EN) is preferred over parenteral nutrition (PN) in hospitalized patients based on International consensus guidelines. We tested the hypothesis that leptin-induced renal sympathetic nerve activation is mediated by PI3K. Oxidation of Cu, Zn-superoxide dismutase by the myeloperoxidase/hydrogen peroxide/chloride system: functional and structural effects. If this was insufficient to reduce their complaints, dose was increased gradually to 75 mg t.i.d.

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There were no marked excesses in overall or site-specific cancer deaths or incident cases. Previous studies suggest that nicotine affects serotonergic signaling, and the intensity dependence (alias loudness dependence) of the auditory evoked N1-P2 potential has been proposed as a marker of serotonergic neurotransmission. Here we report the construction of a series of hybrid mouse-human FIII9-10 pairs that confer varying degrees of conformational stability to FIII9. Indicators of health services and health status were added to describe health system improvements. Astrocytes may contribute to damage by propagating spreading depression or by sending proapoptotic signals to otherwise healthy tissue via gap junction channels. Finally, using RNA probes specific for RSV genomic RNA, we found that viral RNA predominantly localized to viral inclusion bodies but a small percentage also interacted with stress granules during infection. Methylene blue (10(-5) M), an inhibitor of soluble guanylate cyclase, partly abolished relaxation induced by EUK-8. Clinical and treatment characteristics of endometriosis in young patients. We report the case of a 32 depakote sprinkles 125 mg dosage -year-old woman who had a complete exeresis of a 15 cm retroperitoneal myxoid liposarcoma. Is isolated palatal anomaly an indication to screen for 22q11 region deletion?.

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