Bendroflumethiazide. Medical search

A thiazide diuretic with actions and uses similar to those of HYDROCHLOROTHIAZIDE. It has been used in the treatment of familial hyperkalemia, hypertension, edema, and urinary tract disorders. (From Martindale, The Extra Pharmacopoeia, 30th ed, p810)

Agents that inhibit SODIUM CHLORIDE SYMPORTERS. They act as DIURETICS. Excess use is associated with HYPOKALEMIA.

A benzenesulfonamide-phthalimidine that tautomerizes to a BENZOPHENONES form. It is considered a thiazide-like diuretic.

Agents that promote the excretion of urine through their effects on kidney function.

Chemicals used in agriculture. These include pesticides, fumigants, fertilizers, plant hormones, steroids, antibiotics, mycotoxins, etc.

Lists of words, usually in alphabetical order, giving information about form, pronunciation, etymology, grammar, and meaning.

Solid dosage forms, of varying weight, size, and shape, which may be molded or compressed, and which contain a medicinal substance in pure or diluted form. (Dorland, 28th ed)

PRESSURE of the BLOOD on the ARTERIES and other BLOOD VESSELS.

Persistently high systemic arterial BLOOD PRESSURE. Based on multiple readings (BLOOD PRESSURE DETERMINATION), hypertension is currently defined as when SYSTOLIC PRESSURE is consistently greater than 140 mm Hg or when DIASTOLIC PRESSURE is consistently 90 mm Hg or more.

A non-selective beta-adrenergic antagonist with a long half-life, used in cardiovascular disease to treat arrhythmias, angina pectoris, and hypertension. Nadolol is also used for MIGRAINE DISORDERS and for tremor.

Drugs that bind to but do not activate beta-adrenergic receptors thereby blocking the actions of beta-adrenergic agonists. Adrenergic beta-antagonists are used for treatment of hypertension, cardiac arrhythmias, angina pectoris, glaucoma, migraine headaches, and anxiety.

AMINO ALCOHOLS containing the propanolamine (NH2CH2CHOHCH2) group and its derivatives.

Methods for determining interaction between PROTEINS.

Heterocyclic compounds of a ring with SULFUR and two NITROGEN atoms fused to a BENZENE ring. Members inhibit SODIUM-POTASSIUM-CHLORIDE SYMPORTERS and are used as DIURETICS.

A quinazoline-sulfonamide derived DIURETIC that functions by inhibiting SODIUM CHLORIDE SYMPORTERS.

A thiazide diuretic often considered the prototypical member of this class. It reduces the reabsorption of electrolytes from the renal tubules. This results in increased excretion of water and electrolytes, including sodium, potassium, chloride, and magnesium. It is used in the treatment of several disorders including edema, hypertension, diabetes insipidus, and hypoparathyroidism.

Studies used to test etiologic hypotheses in which inferences about an exposure to putative causal factors are derived from data relating to characteristics of persons under study or to events or experiences in their past. The essential feature is that some of the persons under study have the disease or outcome of interest and their characteristics are compared with those of unaffected persons.

Drugs manufactured and sold with the intent to misrepresent its origin, authenticity, chemical composition, and or efficacy. Counterfeit drugs may contain inappropriate quantities of ingredients not listed on the label or package. In order to further deceive the consumer, the packaging, container, or labeling, may be inaccurate, incorrect, or fake.

Exploitation through misrepresentation of the facts or concealment of the purposes of the exploiter.

That segment of commercial enterprise devoted to the design, development, and manufacture of chemical products for use in the diagnosis and treatment of disease, disability, or other dysfunction, or to improve function.

Therapeutic practices which are not currently considered an integral part of conventional allopathic medical practice. They may lack biomedical explanations but as they become better researched some (PHYSICAL THERAPY MODALITIES; DIET; ACUPUNCTURE) become widely accepted whereas others (humors, radium therapy) quietly fade away, yet are important historical footnotes. Therapies are termed as Complementary when used in addition to conventional treatments and as Alternative when used instead of conventional treatment.

Situations or conditions requiring immediate intervention to avoid serious adverse results.

First aid or other immediate intervention for accidents or medical conditions requiring immediate care and treatment before definitive medical and surgical management can be procured.

Activity involved in transfer of goods from producer to consumer or in the exchange of services.

Detailed account or statement or formal record of data resulting from empirical inquiry.

Organizations established by endowments with provision for future maintenance.

Compounds that inhibit the action of prostaglandins.

A group of compounds derived from unsaturated 20-carbon fatty acids, primarily arachidonic acid, via the cyclooxygenase pathway. They are extremely potent mediators of a diverse group of physiological processes.

Control of drug and narcotic use by international agreement, or by institutional systems for handling prescribed drugs. This includes regulations concerned with the manufacturing, dispensing, approval (DRUG APPROVAL), and marketing of drugs.

A metallic element with atomic symbol Fe, atomic number 26, and atomic weight 55.85. It is an essential constituent of HEMOGLOBINS; CYTOCHROMES; and IRON-BINDING PROTEINS. It plays a role in cellular redox reactions and in the transport of OXYGEN.

Recording of the moment-to-moment electromotive forces of the HEART as projected onto various sites on the body's surface, delineated as a scalar function of time. The recording is monitored by a tracing on slow moving chart paper or by observing it on a cardioscope, which is a CATHODE RAY TUBE DISPLAY.

Directions written for the obtaining and use of DRUGS.

A medical specialty concerned with the provision of continuing, comprehensive primary health care for the entire family.

Characterization of the thiazide-sensitive Na(+)-Cl(-) cotransporter: a new model for ions and diuretics interaction. (1/73)

The thiazide-sensitive Na(+)-Cl(-) cotransporter (TSC) is the major pathway for salt reabsorption in the apical membrane of the mammalian distal convoluted tubule. When expressed in Xenopus laevis oocytes, rat TSC exhibits high affinity for both cotransported ions, with the Michaelis-Menten constant (K(m)) for Na(+) of 7.6 +/- 1.6 mM and for Cl(-) of 6.3 +/- 1.1 mM, and Hill coefficients for Na(+) and Cl(-) consistent with electroneutrality. The affinities of both Na(+) and Cl(-) were increased by increasing concentration of the counterion. The IC(50) values for thiazides were affected by both extracellular Na(+) and Cl(-). The higher the Na(+) or Cl(-) concentration, the lower the inhibitory effect of thiazides. Finally, rTSC function is affected by extracellular osmolarity. We propose a transport model featuring a random order of binding in which the binding of each ion facilitates the binding of the counterion. Both ion binding sites alter thiazide-mediated inhibition of transport, indicating that the thiazide-binding site is either shared or modified by both Na(+) and Cl(-). (+info)

Atenolol and bendrofluazide in hypertension. (2/73)

The effect of atenolol, a new beta-1-adrenergic receptor blocking agent, was studied in a double-blind cross-over trial in 24 carefully selected hypertensive outpatients. After a four-week run-in period on matching placebo each patient received atenolol 200 mg/day, atenolol 400 mg/day, a combination of atenolol 200/mg day with bendrofluazide 5 mg/day, and bendrofluazide 5 mg/day alone, according to a random sequence. Atenolol at either dose produced a significantly greater reduction in all blood pressure levels except standing systolic pressure than bendrofluazide alone. There was no statistically significant difference between the effects of the two atenolol doses on either blood pressure or pulse rate. The addition of bendrofluazide to atenolol resulted in a further significant lowering of the blood pressure. A significant effect of thiazide on weight was noted. The study shows that atenolol, a cardioselective beta-blocker of similar potency to propranolol in animals but without membrane-stabilizing or partial agonist acitivity, is an effective and well-tolerated hypotensive agent. (+info)

Improvement in midwall myocardial shortening with regression of left ventricular hypertrophy. (3/73)

Despite normal indices of left ventricular (LV) chamber function, patients with LV hypertrophy (LVH) due to hypertension are thought to have depressed midwall systolic shortening compared with normotensives. The aims of the present study were (1) to confirm this observation and (2) to assess the effects of antihypertensive therapy that cause regression of LVH on LV systolic function assessed at both the midwall and endocardium. Thirty-eight previously untreated hypertensive subjects with LVH underwent echocardiography and were compared with 38 normotensive control subjects. Comparisons between the group with LVH and the control group revealed no significant differences in cardiac output (4. 32+/-0.23 versus 4.55+/-0.21 L/min), ejection fraction (62.5+/-2% versus 66.4+/-1.07%), or endocardial fractional shortening (34.5+/-1.45% versus 37.0+/-0.82%), but shortening assessed at the midwall was significantly less in the group with LVH (17.9+/-1.11% versus 21.6+/-0.63%, P<0.01). Subsequently, 32 patients with uncontrolled hypertension (24 previously untreated and 8 on existing antihypertensive therapy) underwent treatment with ramipril, with the addition of felodipine and bendrofluazide if required, to reduce blood pressure to <140/90 mm Hg. These 32 patients underwent echocardiography at baseline, after blood pressure control, and after an additional 6 months of tight blood pressure control. Good blood pressure control was achieved after 6 months compared with baseline (143/86+/-2.8/1.4 versus 174/103+/-4.1/1.9 mm Hg; P<0.01) with significant regression of LV mass index (124+/-3.4 versus 145+/-3.8 g/m(2), P<0.01). LV fractional shortening assessed at the midwall improved with regression of LVH (21.9+/-0.84 and 18.7+/-1. 19%, P<0.05), with posttreatment midwall shortening being similar to that of the normal control subjects evaluated in the first study. Hypertensive patients with LVH have depressed midwall systolic shortening despite normal indices of LV chamber function. Regression of LVH after good blood pressure control improved midwall shortening to normal levels. (+info)

Electrical potential difference, sodium absorption and potassium secretion by the human rectum during carbenoxolone therapy. (4/73)

The transmucosal electrical potential difference (pd) and the sodium and potassium net fluxes were measured in the rectum of subjects taking carbenoxolone. There was a rise in transmucosal pd persisting throughout treatment in all subjects which was accompanied by an increase in sodium absorption and potassium secretion. Comparison of the pd changes produced by carbenoxolone with those due to the mineralocorticoid 9-alpha-fluorocortisol showed that carbenoxolone had about 1/1000th the potency on a weight basis and the two drugs appeared to be additive in their effects. Topical instillation of carbenoxolone into the rectum produced an elevation of pd which persisted for three days. Amiloride and bendrofluazide did not interfere with these actions of carbenoxolone but spironolactone abolished them. One patient who developed fluid retention and hypokalaemia had a rectal pd similar to that of the other patients who had no side effects. (+info)

Nebivolol reverses endothelial dysfunction in essential hypertension: a randomized, double-blind, crossover study. (5/73)

BACKGROUND: Vascular endothelial dysfunction may predict future atherosclerosis. Hence, an antihypertensive agent that reverses endothelial dysfunction and lowers blood pressure might improve the prognosis of patients with hypertension. We hypothesized that nebivolol, a vasodilating beta-blocker, could improve endothelial dysfunction. We tested this hypothesis by comparing the effects of nebivolol and atenolol on endothelial function. METHODS AND RESULTS: Twelve hypertensive patients with a mean ambulatory blood pressure of 154+/-7/97+/-10 mm Hg were randomized after a 2-week placebo run-in period (baseline) in a double-blind, crossover fashion to 8-week treatment periods with either 5 mg of nebivolol with 2.5 mg of bendrofluazide or 50 mg of atenolol with 2.5 mg of bendrofluazide. Forearm venous occlusion plethysmography and intra-arterial infusions of acetylcholine and N(G)-monomethyl-L-arginine (L-NMMA) were used to assess stimulated and basal endothelium-dependent nitric oxide release, respectively. Sodium nitroprusside was used as an endothelium-independent control. Nebivolol/bendrofluazide and atenolol/bendrofluazide each lowered the clinic blood pressure to the same extent (132+/-7/82+/-6 and 132+/-9/83+/-8 mm Hg, respectively; P<0.001 from baseline). The vasodilatory response to acetylcholine was significantly increased with nebivolol/bendrofluazide (maximum percentage change in forearm blood flow [mean+/-SEM], 435+/-27%, P<0.001) but not with atenolol/bendrofluazide. Similarly, the endothelium-dependent vasoconstrictive response to L-NMMA was significantly improved only with nebivolol treatment (percentage change in forearm blood flow, -54+/-5%; P<0.001). The response to sodium nitroprusside was not different between treatments, suggesting that the endothelium-independent pathway was unaffected. CONCLUSIONS: Nebivolol/bendrofluazide increased both stimulated and basal endothelial nitric oxide release, whereas for the same degree of blood pressure control, atenolol/bendrofluazide had no effect on nitric oxide bioactivity. Thus, nebivolol may offer additional vascular protection in treating hypertension. (+info)

Role of sodium depletion in acute antidiuretic effect of bendroflumethiazide in rats with nephrogenic diabetes insipidus. (6/73)

The mechanisms underlying the acute antidiuretic response to bendroflumethiazide (BFTZ; 0.25 mg/h for 3 h) in rats with nephrogenic diabetes insipidus (NDI) was investigated. NDI was induced in conscious chronically instrumented female Wistar rats either by chronic lithium administration (40-60 mmol Li/kg of diet for 4 weeks) or by acute infusion of V2 antagonist OPC-31260 (0.2 mg/h). Renal clearance experiments were performed in conscious rats instrumented with permanent catheters. During experiments total body water content was held constant by i.v. replacement of urine production (V) with 150 mM glucose. One group in addition received i.v. replacement of urinary sodium losses. In both models of NDI, BFTZ-induced antidiuresis was associated with a decrease in the delivery of tubular fluid to the distal nephron, as measured by lithium clearance (C(Li)). Both the antidiuresis and the decrease in C(Li) could be prevented by sodium replacement. BFTZ did not affect distal water handling as measured by V/C(Li). BFTZ did not induce antidiuresis in normal rats with water diuresis. It is concluded that in rats with NDI, thiazide-induced antidiuresis can be entirely explained by a fall in distal delivery of tubular fluid related to sodium depletion. This contrasts the response in rats with central diabetes insipidus, where thiazides in addition increase distal water reabsorption. (+info)

Monitoring one-year compliance to antihypertension medication in the Seychelles. (7/73)

OBJECTIVE: To examine the compliance to medication among newly diagnosed hypertensive patients screened from the general population of the Seychelles, a rapidly developing country. METHODS: Among the 1067 participants to a population-based survey for cardiovascular risk factors, hypertension was discovered in 50 (previously unaware of having hypertension and having blood pressure > or = 160/95 mmHg over 3 visits). These 50 patients were placed on a daily one-pill regimen of medication (bendrofluazide, atenolol, or a combination of hydrochlorothiazide and atenolol) and compliance to the regimen was assessed over 12 months using electronic pill containers. Satisfactory compliance was defined as taking the medication on 6 or 7 days a week on average (which corresponds to a mean compliance level of > or = 86%). FINDINGS: In the first month, fewer than half (46%) of the new hypertension patients achieved satisfactory compliance, and only about one-quarter (26%) achieved this level by the twelfth month. Compliance was better among the 23 participants who regularly attended medical follow-up, with nearly three-quarters of these patients (74%) achieving satisfactory compliance during the first month and over one-half (55%) by the twelfth month. There was a direct association between mean 12-month compliance level and having a highly skilled occupation; having good health awareness; and regularly attending medical appointments. In contrast, there was an inverse relationship between mean compliance level and heavy drinking. CONCLUSION: The low proportion of people selected from the general population who were capable of sustaining satisfactory compliance to antihypertension medication may correspond to the maximum effectiveness of medication interventions based on a screening and treatment strategy in the general population. The results stress the need for both high-risk and population approaches to improve hypertension control. (+info)

Von Willebrand factor, soluble P-selectin, and target organ damage in hypertension: a substudy of the Anglo-Scandinavian Cardiac Outcomes Trial (ASCOT). (8/73)

To investigate the relationship between soluble markers of platelet, endothelial and rheological function, and target organ damage and their response to intensified management in a population of middle-age hypertensive patients at high risk of cardiovascular complications, we studied 382 consecutive patients (308 men; mean age, 63 years, SD 8) along with 60 normotensive controls free of cardiovascular disease. Patients were divided into those with target organ damage (TOD; n=107) and those free of end-organ damage. Plasma levels of soluble P-selectin (sP-sel), a marker of platelet activation, and von Willebrand factor (vWF), an index of endothelial damage/dysfunction (both enzyme-linked immunosorbent assay), and the rheological indices fibrinogen, plasma viscosity, hematocrit, platelet, and white cell count were measured. In 53 patients, variables were further measured after 6 months of intensified cardiovascular risk management. Patients with TOD had significantly higher vWF, 137 (SD 33) versus 125 (SD 33) IU/dL (P=0.002,) and a greater proportion of smokers, 31% versus 16% (P=0.002). There were no statistically significant differences in plasma viscosity, fibrinogen, hematocrit, white blood cell count, platelet count, or sP-sel between the 2 subgroups. In multivariate analysis, vWF was a significant independent predictor for TOD. After 6 months of intensified management in 53 patients who entered the trial, there were significant reductions in systolic blood pressure, total cholesterol, hematocrit, plasma viscosity, sP-sel, and vWF (all P<0.01) but no significant change in fibrinogen. In conclusion, there is a relationship between TOD and endothelial damage/dysfunction in hypertension. Intensified management results in improvements in hemorheology, endothelial and platelet function. (+info)

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What is the most important information I should know about bendroflumethiazide and nadolol? (cigna.com)
You should not use bendroflumethiazide and nadolol if you have a serious heart condition such as "AV block" (2nd or 3rd degree), uncontrolled heart failure, slow heartbeats that have caused you to faint, or if your heart cannot pump blood properly. (cigna.com)
Bendroflumethiazide and nadolol is a combination medicine used to treat high blood pressure (hypertension). (cigna.com)
Bendroflumethiazide and nadolol may also be used for purposes not listed in this medication guide. (cigna.com)
What should I discuss with my healthcare provider before taking bendroflumethiazide and nadolol? (cigna.com)
Bendroflumethiazide and nadolol can pass into breast milk and may harm a nursing baby. (cigna.com)
Bendroflumethiazide and nadolol is not approved for use by anyone younger than 18 years old. (cigna.com)
How should I take bendroflumethiazide and nadolol? (cigna.com)
You may take bendroflumethiazide and nadolol with or without food. (cigna.com)
Prolonged illness can lead to a serious electrolyte imbalance, making it dangerous for you to use bendroflumethiazide and nadolol. (cigna.com)
If you need surgery or medical tests, tell the doctor ahead of time that you are taking bendroflumethiazide and nadolol. (cigna.com)

When used to treat hypertension, Bendroflumethiazide tablets are often combined with other medications, such as beta blockers. (superdrug.com)
Does the aldosterone: renin ratio (ARR) predict the efficacy of spironolactone over bendroflumethiazide in hypertension? (dundee.ac.uk)

Bendroflumethiazide comes as 2.5mg and 5mg tablets. (netdoctor.co.uk)
Bendroflumethiazide, as the name suggests, is a thiazide diuretic, which are treatments known as water tablets. (121doc.com)
Your doctor may start you off on the lowest dose of Bendroflumethiazide which is 2.5mg tablets and this may then be increased to 5mg or 10mg, should the results be unsatisfactory. (121doc.com)
One of our UK based doctors will review your answers and confirm whether it is safe for you to continue your treatment with Bendroflumethiazide tablets. (superdrug.com)
How Are Bendroflumethiazide Tablets Taken? (superdrug.com)
When you are first prescribed Bendroflumethiazide, your GP will explain how often you have to take your tablets. (superdrug.com)
In these cases your doctor may advise treatment in the form of Bendroflumethiazide tablets. (zentherapycenter.com)

Bendroflumethiazide is a diuretic medicine. (netdoctor.co.uk)
Bendroflumethiazide is a type of medicine called a thiazide diuretic. (netdoctor.co.uk)
Bendroflumethiazide is a thiazide diuretic (water pill) that helps prevent your body from absorbing too much salt, which can cause fluid retention. (cigna.com)
Bendroflumethiazide is a generic diuretic also known as Aprinox. (121doc.com)
Bendroflumethiazide is a diuretic used to treat high blood pressure. (superdrug.com)
Bendroflumethiazide is a thiazide diuretic for high blood pressure . (superdrug.com)

People who stand or sit for long periods of Bendroflumethiazide may notice some foot or ankle swelling at the end of the day, this is known as peripheral oedema. (zentherapycenter.com)

The active ingredient, bendroflumethiazide, falls into the category of medicines known as thiazide diuretics. (zentherapycenter.com)

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Your insulin or diabetes medication needs may change while you are taking bendroflumethiazide and propranolol. (cigna.com)
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Bendroflumethiazide is a complete analogue of Bendroflumethiazide Bristol. (zentherapycenter.com)
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This is fairly common, Bendroflumethiazide fluid retention symptoms are often persistent and can be found in other parts of the body. (zentherapycenter.com)

Bendroflumethiazide will usually make you need to go to the toilet one to two hours after taking a dose and then again a few hours later. (netdoctor.co.uk)

Bendroflumethiazide helps the body to remove this excess fluid. (netdoctor.co.uk)
Bendroflumethiazide can also be used to remove excess fluid that accumulates in your body if you have kidney disease or cirrhosis of the liver. (netdoctor.co.uk)

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You'll usually need to keep taking bendroflumethiazide on a long-term basis to keep your condition under control. (netdoctor.co.uk)
Bendroflumethiazide is intended to help patients who need to lower their BP to avoid serious health problems, which may include long term cardiovascular disease. (121doc.com)

Our Corzide (nadolol and bendroflumethiazide) Side Effects Drug Center provides a comprehensive view of available drug information on the potential side effects when taking this medication. (rxlist.com)
CORZIDE (Nadolol and Bendroflumethiazide Tablets) is indicated for the treatment of hypertension, to lower blood pressure. (pfizermedicalinformation.com)
CORZIDE (Nadolol and Bendroflumethiazide Tablets) is not indicated for initial therapy of hypertension. (pfizermedicalinformation.com)
Bendroflumethiazide in CORZIDE is 30 percent more bioavailable than that of 5 mg Naturetin tablets. (pfizermedicalinformation.com)
Conversion from 5 mg NATURETIN to CORZIDE represents a 30 percent increase in dose of bendroflumethiazide. (pfizermedicalinformation.com)
The initial dose of CORZIDE (Nadolol and Bendroflumethiazide Tablets) may therefore be the 40 mg/5 mg tablet once daily. (pfizermedicalinformation.com)
CORZIDE (Nadolol and Bendroflumethiazide Tablets) for oral administration combines two antihypertensive agents: CORGARD ® (nadolol), a nonselective beta-adrenergic blocking agent, and NATURETIN ® (bendroflumethiazide), a thiazide diuretic-antihypertensive. (pfizermedicalinformation.co.cr)
CORZIDE (Nadolol and Bendroflumethiazide Tablets) for oral administration combines two antihypertensive agents: CORGARD? (nih.gov)

are they linked after having successful surgery for renal artery stenosis consultant put me on verapamil and bendrofluazide now called bendroflumethiazide to control - 82% more. (medications.com)
The drug most commonly prescribed was bendroflumethiazide (bendrofluazide). (innovations-report.com)

In the US, Bendroflumethiazide (bendroflumethiazide/nadolol systemic) is a member of the drug class thiazide diuretics and is used to treat Edema and High Blood Pressure . (drugs.com)
Bendroflumethiazide is a thiazide diuretics that can be purchased quickly online in either 2.5mg or 5mg dosage options. (onlineclinic.co.uk)
The active ingredient, bendroflumethiazide, falls into the category of medicines known as thiazide diuretics. (zentherapycenter.com)
and thiazide diuretics including chlortaliodone and bendroflumethiazide. (livestrong.com)

Bendroflumethiazide is a tablet designed to reduce high blood pressure. (onlineclinic.co.uk)
The usual dose of Bendroflumethiazide per day is one tablet. (onlineclinic.co.uk)
Bendroflumethiazide is a water tablet meaning it adjusts the amount fluid that is transported around the body, reducing any pressure in the blood and on the heart. (onlineclinic.co.uk)
Being known as a "water tablet", Bendroflumethiazide is highly effective at transporting fluids around the body to help reduce blood pressure and lessen any pressure the condition has caused on the heart. (onlineclinic.co.uk)
0115-5311 Bendroflumethiazide 5 mg / Nadolol 40 mg Oral Tablet by Global Pharmaceuticals, Division of Impax Laboratories, Inc. (medschat.com)
0115-5322 Bendroflumethiazide 5 mg / Nadolol 80 mg Oral Tablet by Global Pharmaceuticals, Division of Impax Laboratories, Inc. (medschat.com)
Formulations: 40 mg and 80 mg nadolol per tablet combined with 5 mg bendroflumethiazide. (pfizermedicalinformation.co.cr)

Bendroflumethiazide and other thiazides may cause a number of metabolic disturbances especially at high doses. (gafacom.website)

The active ingredient of the same brand name - bendroflumethiazide PhEur - has either 2.5mg or 5mg of this element present. (onlineclinic.co.uk)

There are 0 terms under the parent term 'Bendroflumethiazide' in the ICD-10-CM Drugs Index . (icd.codes)
It is also contraindicated in patients who have previously demonstrated hypersensitivity to bendroflumethiazide or other sulfonamide-derived drugs. (pfizermedicalinformation.com)
A list of drugs that interact with Bendroflumethiazide. (evidence.nhs.uk)

Prevention of cardiovascular events with an antihypertensive regimen of amlodipine adding perindopril as required versus atenolol adding bendroflumethiazide as required, in the Anglo-Scandinavian Cardiac Outcomes Trial-Blood Pressure Lowering Arm (ASCOT-BPLA): a multicentre randomised controlled trial. (acpjc.org)
Amlodipine, 5 to 10 mg, adding perindopril, 4 to 8 mg as required ( n = 9639), or atenolol, 50 to 100 mg, adding bendroflumethiazide, 1.25 to 2.5 mg, and potassium as required ( n = 9618). (acpjc.org)
The Anglo-Scandinavian Cardiac Outcomes Trial-Blood Pressure Lowering Arm (ASCOT-BLA) was a 2005 landmark trial that compared the effects of the established therapy of the combination of atenolol and bendroflumethiazide to the new drug combination of amlodipine and perindopril. (wikipedia.org)

Bendroflumethiazide helps the body to remove this excess fluid. (netdoctor.co.uk)
Bendroflumethiazide can also be used to remove excess fluid that accumulates in your body if you have kidney disease or cirrhosis of the liver. (netdoctor.co.uk)
This is fairly common, Bendroflumethiazide fluid retention symptoms are often persistent and can be found in other parts of the body. (zentherapycenter.com)

Prolonged illness can lead to a serious electrolyte imbalance, making it dangerous for you to use bendroflumethiazide and nadolol. (cigna.com)

As the global leader in prescription drug savings, Mail Order Meds believes in going the extra mile to provide even better value to our customers when they order discount Bendroflumethiazide from our online pharmacy. (mailordermeds.com)

There are indications that Bendroflumethiazide is fairly extensively metabolized about 30% is excreted unchanged in the urine. (gafacom.website)

The study is a double-blind, randomised, crossover, controlled trial that will randomise 120 hypertensive subjects to 12 weeks treatment with spironolactone 50 mg once daily and 12 weeks treatment with bendroflumethiazide 2.5 mg once daily. (biomedcentral.com)
Primary Objective - To test the hypothesis that the aldosterone: renin ratio predicts the antihypertensive response to spironolactone, specifically that the effect of spironolactone 50 mg is greater than that of bendroflumethiazide 2.5 mg in hypertensive subjects with high aldosterone: renin ratios. (biomedcentral.com)

Bendroflumethiazide is well-received by the vast majority of users, however some experience side effects such as nausea, muscle cramps and thirst. (onlineclinic.co.uk)

Please note that our service is only suitable for patients who have been taking Bendroflumethiazide for at least three months and whose blood pressure is well controlled. (superdrug.com)

Bendroflumethiazide should be given to a pregnant woman only if clearly needed. (rxwiki.com)

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Characterization of the thiazide-sensitive Na(+)-Cl(-) cotransporter: a new model for ions and diuretics interaction. (1/73)

Atenolol and bendrofluazide in hypertension. (2/73)

Improvement in midwall myocardial shortening with regression of left ventricular hypertrophy. (3/73)

Electrical potential difference, sodium absorption and potassium secretion by the human rectum during carbenoxolone therapy. (4/73)

Nebivolol reverses endothelial dysfunction in essential hypertension: a randomized, double-blind, crossover study. (5/73)

Role of sodium depletion in acute antidiuretic effect of bendroflumethiazide in rats with nephrogenic diabetes insipidus. (6/73)

Monitoring one-year compliance to antihypertension medication in the Seychelles. (7/73)

Von Willebrand factor, soluble P-selectin, and target organ damage in hypertension: a substudy of the Anglo-Scandinavian Cardiac Outcomes Trial (ASCOT). (8/73)

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Characterization of the thiazide-sensitive Na(+)-Cl(-) cotransporter: a new model for ions and diuretics interaction. (1/73)

Atenolol and bendrofluazide in hypertension. (2/73)

Improvement in midwall myocardial shortening with regression of left ventricular hypertrophy. (3/73)

Electrical potential difference, sodium absorption and potassium secretion by the human rectum during carbenoxolone therapy. (4/73)

Nebivolol reverses endothelial dysfunction in essential hypertension: a randomized, double-blind, crossover study. (5/73)

Role of sodium depletion in acute antidiuretic effect of bendroflumethiazide in rats with nephrogenic diabetes insipidus. (6/73)

Monitoring one-year compliance to antihypertension medication in the Seychelles. (7/73)

Von Willebrand factor, soluble P-selectin, and target organ damage in hypertension: a substudy of the Anglo-Scandinavian Cardiac Outcomes Trial (ASCOT). (8/73)

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