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Also known as:  Tamsulosin.


Flomax is a perfect remedy in struggle against symptoms of HPB. Its target is to treat benign prostatic hyperplasia or enlarged prostate.

This remedy is acting by relaxing the blood vessels and muscles of bladder and prostate making urination easier. It is adrenergic blocker.

Flomax is also known as Tamsulosin, Veltam, Flomaxtra, Urimax.

Generic name of Flomax is Tamsulosin.

Brand name of Flomax is Flomax.


Flomax is available in capsules and liquid form.

Take Flomax capsules orally.

Do not crush or chew it.

Take Flomax once a day 30 minutes after the meal, at the same time every day with water.

If you want to achieve most effective results do not stop taking Flomax suddenly.


If you overdose Flomax and you don't feel good you should visit your doctor or health care provider immediately. Symptoms of Flomax overdosage: fainting, fast heartbeat, cold skin, migraine, lightheadedness, dyspepsia, blurred vision, clammy.


Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F) away from moisture and heat. Throw away any unused medicine after the expiration date. Keep out of reach of children.

Side effects

The most common side effects associated with Flomax 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.


Do not take Flomax if you are allergic to Flomax components.

Do not take Flomax if you're pregnant or you plan to have a baby, or you are a nursing mother. Flomax can harm your baby.

Be careful with Flomax if you suffer from or have a history of prostate cancer, liver disease, kidney disease.

If you are going to have a surgery you should be careful with Flomax.

Try to be careful using Flomax if you take alfusozin (such as Uroxatral), doxazosin (such as Cardura), prazosin (such as Minipress), Terazosin (such as Hytrin), warfarin (such as Coumadin); antibiotics such as erythromycin (such as E.E.S., E-Mycin, Erythrocin, Ery-Tab), azithromycin (such as Zithromax), clarithromycin (such as Biaxin), itraconazole (such as Sporanox), ciprofloxacin (such as Cipro), ketoconazole (such as Nizoral); heart or blood pressure medicines such as verapamil (such as Isoptin, Calan, Verelan, Covera), diltiazem (such as Tiazac, Cardizem, Dilacor); cimetidine (such as Tagamet); HIV /AIDS medicines such as ritonavir (such as Norvir), indinavir (such as Crixivan), saquinavir (such as Fortovase, Invirase), nelfinavir (such as Viracept); cyclosporine (such as Sandimmune, Gengraf, Neoral); antidepressants such as fluvoxamine (such as Luvox), citalopram (such as Celexa), paroxetine (such as Paxil), escitalopram (such as Lexapro), sertraline (such as Zoloft), fluoxetine (such as Sarafem, Prozac); metronidazole (such as Flagyl, Protostat).

Avoid alcohol.

Keep Flomax away from children and don't give it to other people for using.

Do not stop taking Flomax suddenly.

flomax renal dosing

Between January 2004 and September 2005, 114 patients with symptomatic distal ureteral stones with a >/=5mm diameter were enrolled in this prospective study and divided into four groups based on the urologist (of four) who treated them in the emergency unit. Group A (33 patients) received tamsulosin (0.4mg daily), group B (24 patients) received deflazacort (30mg daily), group C (33 patients) received both (0.4mg tamsulosin+30mg deflazacort daily), and control group D (24 patients) received only analgesics. The treatment duration was 10 d to prevent the side-effects of prolonged corticosteroid therapy. The end points were the expulsion rate, analgesic consumption, number of ureteroscopies, and safety.

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To examine the frequency of and risk factors for nocturia in patients with symptomatic benign prostatic hyperplasia (BPH), and the degree of improvement of nocturia after treatment for BPH.

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Observational retrospective study that took place over a period of 2 years (july 2009-july 2011) and reviewed 2484 eyes that underwent cataract surgery. A number of 1199 eyes were from 1049 male patients.

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All patients completed the study and there were no major side-effects. There was no difference in age, stone position or stone size among the groups. Multivariate analysis using a Cox proportional hazards model indicated that the probability of stone expulsion for 1 month was increased 2.38 times (95% confidence interval 1.23-4.61) by naftopidil compared with control therapy alone (p = 0.01).

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41 men were enrolled in the study and they were subjected to either watchful waiting (group 1) or alpha(1)-adrenergic receptor blocker therapy (group 2 with alfuzosin; group 3 with tamsulosin). The patients were investigated by symptom evaluation using the International Prostate Symptom Score (IPSS) and quality of life score (QOL), uroflowmetry and UEBW. The parameters were assessed again 3 months after initiation of treatment and compared with the initial values.

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Alfuzosin provided a significantly higher stone-free rate than the control treatments (RR: 1.85; 95% confidence interval [CI], 1.35-2.55; p<0.001), and a shorter stone expulsion time (Weighted mean difference [WMD]: -4.20 d, 95%CI, -6.19 to -2.21; p<0.001), but it has a higher complication rate (RR: 2.02; 95% CI, 1.30-3.15; p<0.01). When Alfuzosin was compared to Tamsulosin, there was no significant difference in terms of stone-free rate (RR: 0.90; 95% CI, 0.79-1.02; p = 0.09) as well as the stone expulsion time (WMD: 0.52 d, 95%CI, -1.61 to 2.64; p = 0.63). The adverse effects of Alfuzosin were similar to those of Tamsulosin (RR: 0.88; 95% CI, 0.61-1.26; p = 0.47).

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Six-hundred thirty-eight men were randomized. Urgency was reduced by 2.2 and 2.4 episodes in the TAM+SOL 2.5 and 5 mg groups, respectively. The TAM+SOL 5 mg group showed significant improvement compared with TAM+PBO (-2.4 vs -1.9, P=.049). The number of micturitions in both TAM+SOL groups were significantly reduced compared with TAM+PBO (both P<.001). IPSS storage symptom score and OABSS significantly improved in both TAM+SOL groups compared with TAM+PBO. Changes in IPSS voiding symptom score and Qmax. were similar in all groups. Four patients (1.9%) in the TAM+SOL 5 mg group had urinary retention, but all recovered after catheterization.

flomax dosing

The objective of this study is to assess the efficacy of an alpha-1 adrenergic receptor blocking agent on the spontaneous passage of proximal ureteral calculi < or =10 mm. 92 patients having single radio-opaque proximal ureteral stone < or =10 mm were randomized into two groups. Group 1 patients (n = 50) were followed with classical conservative approach and patients in Group 2 (n = 42) additionally received tamsulosin, 0.4 mg/day during 4 weeks follow-up. The stone passage rates, stone expulsion time, VAS score, change in colic episodes, and hospital re-admission rates for colicky pain were compared. The patients were furthermore stratified according to stone diameters <5 and 5-10 mm. The data of these subgroups were also compared. Stone expulsion rates showed statistically significant difference between tamsulosin receivers and non-receivers (35.7 vs 30%, p = 0.04). Time to stone expulsion period was also shortened in those receiving tamsulosin (8.4 +/- 3.3 vs 11.6 +/- 4.1 days, p = 0.015). Likewise, the mean VAS score and renal colic episodes during follow-up period were significantly diminished in Group 2 patients (4.5 +/- 2.3 vs 8.8 +/- 2.9, p < 0.01 and 66.6 vs 36%, p = 0.001, respectively). Among the stones <5 mm, tamsulosin receiving patients had higher spontaneous passage rate (71.4 vs 50%, p < 0.001). The prominent effect of tamsulosin on the 5-10 mm stones was the relocation of the stones to a more distal part of ureter (39.3 vs 18.7%, p = 0.001). Administration of tamsulosin in the medical management of proximal ureteral calculi can facilitate the spontaneous passage rate in the stone <5 mm and the relocation of the stones between 5 and 10 mm to more distal part of the ureter.

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Of the 112 patients, 81 and 31 had PV of < 35 and ≥ 35 mL, respectively. The IPSS was significantly improved in patients with PV of < 35 mL (17.8 ± 5.9 at baseline, 13.5 ± 7.0 at 4 weeks, 11.9 ± 6.1 at 3 months) and in those with PV of ≥ 35 mL (17.4 ± 6.7 at baseline, 13.1 ± 7.0 at 4 weeks, 13.4 ± 6.2 at 3 months). There was no significant difference in the changes of the IPSS between the groups in a combined analysis model (P = 0.559). In addition, the model revealed no significant differences in changes in the QOL index, BPI, Qmax and PVR.

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flomax prostatitis reviews 2017-06-27

To investigate the add-on effect of solifenacin for Cefixime E Medicine Japanese men with remaining overactive bladder (OAB) symptoms after tamsulosin monotherapy for lower urinary tract symptoms (LUTS) suggestive of benign prostatic obstruction (BPO) in real-life clinical practice.

flomax generic 2017-05-18

This suggests that even after six hours of administration of tamsulosin, and determining of lung function parameters, the activity of alpha1A and alpha1B-adrenergic receptor Atarax 10mg Reviews in the smooth bronchial musculature has not changed in patients with increased bronchial reactibility.

flomax medication alternatives 2016-08-29

Most men who live to middle age and beyond will ultimately develop lower urinary tract symptoms (LUTS) secondary to benign prostatic hyperplasia (BPH), and many will also experience sexual dysfunction. Clinical studies indicate that most patients will experience improvement in BPH-related LUTS with alpha-adrenergic blockade or 5alpha-reductase inhibition. Recent studies suggest that alpha-blockers and 5alpha-reductase inhibitors may help to slow the progression of LUTS; 5alpha-reductase inhibitors reduce the need for surgery and complications, such as acute urinary retention. Third-generation alpha-blockers (alfuzosin, tamsulosin) are infrequently associated with cardiovascular side effects, in contrast to their predecessors (doxazosin, terazosin, prazosin). This may provide an advantage for consideration as firstline therapy. alpha-Blocker therapy may also improve sexual functioning, with the exception of ejaculation disorders, predominantly associated with subtypeselective alpha-blockers. By contrast, 5alpha-reductase inhibition is not recommended for men without demonstrable prostatic enlargement, may be associated with a long delay between treatment initiation and LUTS improvement, and is clearly associated with sexual side effects, including decreased libido, ejaculatory dysfunction, and erectile dysfunction. When choosing appropriate pharmacotherapy, the clinician should consider not Diamox With Alcohol only the expeditious relief of the presenting symptoms but also the patient's quality of life, including sexual function and potential long-term outcomes, such as acute urinary retention and the need for surgical intervention.

flomax 20 mg 2017-04-01

In men with LUTS/BPH who have moderate-to-severe storage symptoms and voiding symptoms, the reduction in symptoms with a once-daily FDC of solifenacin and TOCAS was associated with consistent patient-relevant improvements in HRQoL Avodart Dutasteride Capsules compared with placebo and TOCAS monotherapy.

flomax 128 mg 2015-02-18

Clinical practices in Los Altos and San Rafael Paxil Max Dose , California, USA.

flomax 8 mg 2017-08-11

A 74 year-old man with prostate hypertrophy developed frequent attacks of amaurosis fugax in the left eye. Attacks only occurred in a standing position, but not when sitting or lying. He had taken tamsulosin hydrochloride for prostate hypertrophy and had orthostatic hypotension. After stopping the administration of tamsulosin hydrochloride and starting anthithorombotic theraphy, his orthostatic hypotension disappeared and the frequency of attacks decreased. Cerebral angiography demonstrated 95% stenosis and distal collapse of the left internal carotid artery (ICA), with collateral flow to the left middle cerebral artery from the right ICA through the anterior communicating artery. We thus postulated that a hemodynamic mechanism played an important role in Terramycin Reviews the development of the amaurosis fugax which disappeared after carotid endarterectomy.

harnal drug flomax 2015-01-03

Improvements from baseline were seen in all primary efficacy parameters and were maintained throughout the study. The changes from baseline for the total AUA symptom score and Qmax were statistically significant (P <0.001) at all 3-month intervals. Tamsulosin was well tolerated, and the incidence of adverse events did not increase over time. The mean sitting Medicine Zovirax vital signs did not vary from baseline or relative to the treatment duration.

flomax 400 mg 2015-03-06

The chiral separation of racemic tamsulosin hydrochloride (TH) was carried out using cyclodextrin (CD)-mediated capillary electrophoresis (CE) with DAD at 200 nm. The best separation of enantiomers of the studied compound was achieved at 20 kV with 30 cm x 50 microm I.D. polyacrylamide (PAA)-coated fused-silica capillary (effective length 20 cm) and running buffer with sulfated-beta-CD (S-beta-CD) as chiral selector. Other selected native or derivatized CDs were also tested: beta-CD (5, 15 mmol l(-1)), carboxymethyl-beta-CD (5, 30 mmol l(-1)), dimethyl-beta-CD (15 mmol l(-1)) and hydroxypropyl-beta-CD (5, 30 mmol l(-1)). Several parameters such as capillary pretreatment, buffer type and concentration, pH of background electrolyte, methanol content, separation temperature and voltage, were optimized. The excellent baseline separation of chiral TH was successfully achieved within 12 min using 100 mmol l(-1) phosphate buffer with pH 2.5 containing Inderal Medication 1.7 mmol l(-1) S-beta-CD. Rectilinear calibration range was 50.0-500.0 mumol l(-1) of each enantiomer (r = 0.9993-0.9996). The method was applied to the assay of R-TH in Omnic, capsules (nominal content 0.4 mg per capsule) with R.S.D. 2.75% (n = 6), recovery 99.3-101.7% and it was suitable for the chiral purity control of the active enantiomer in the pharmaceutical.

flomax generic alternative 2015-01-28

To compare the efficacy and tolerability of the alpha 1 A-subtype selective drug tamsulosin with the nonsubtype-selective agent alfuzosin in the treatment of patients with lower urinary tract symptoms (LUTS) suggestive of bladder outlet obstruction ( Omnicef Pediatric Dose BOO), often termed symptomatic benign prostatic hyperplasia (BPH).

flomax related drugs 2016-05-07

To investigate the association between factors influencing prostate-specific antigen (PSA) testing prevalence including prostate cancer risk Ceftin Dosing Adults factors (age, ethnicity, obesity) and non-risk factors (social deprivation and comorbidity).

flomax 10 mg 2016-03-23

To investigate the changes in the α1-adrenoceptor and nerve Omnicef Kids Dose growth factor (NGF)/NGF precursor (proNGF) pathway in the urethra after diabetes induction.

flomax overdose 2015-06-29

This prospective study was performed between January 2001 and December 2004. It included 405 patients who were at least 50 years old with lower urinary tract symptoms. This study was divided into 2 phases. In phase 1 patients received a 0.4 mg tamsulosin capsule daily after breakfast for at least 3 months. The second phase of this study was performed in the 30 patients with abnormal ejaculation. In this phase these patients received 0.4 mg tamsulosin once daily every other day. Patients were assessed at study entry and at study week 6.