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Benazeplus (Amiloride)
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Benazeplus

Benazeplus is in a class of medications called diuretics. It works by causing the kidneys to get rid of unneeded water and salt from the body into the urine, but reduces the loss of potassium.

Other names for this medication:
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Also known as: Amiloride

Description

Benazeplus is a diuretic (water pill) and a combination of a potassium-sparing diuretic (amiloride) and a thiazide diuretic (hydrochlorothiazide). It works by making the kidneys eliminate sodium (salt) and water from the body, which helps to lower blood pressure. The amiloride component helps minimize potassium loss. Brand name of Benazeplus is Benazeplus.

Dosage

Take Benazeplus by mouth with food. Benazeplus may increase the amount of urine or cause you to urinate more often when you first start taking it. To keep this from disturbing your sleep, try to take your dose before 6 pm. If you want to achieve most effective results do not stop taking Benazeplus suddenly.

Overdose

If you overdose Benazeplus and you don't feel good you should visit your doctor or health care provider immediately.

Storage

Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F) away from moisture, light and heat. Do not freeze. Keep container closed tightly. Throw away any unused medicine after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Benazeplus 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

Do not take Benazeplus if you are allergic to Benazeplus components or to any ingredient in Benazeplus or any other sulfonamide (eg, sulfamethoxazole). Be careful with Benazeplus if you're pregnant or you plan to have a baby, or you are a nursing mother. Be careful with Benazeplus if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement. Be careful with Benazeplus if you have allergies to medicines, foods, or other substances. Be careful with Benazeplus if you have cirrhosis or liver problems, diabetes, gout, kidney problems or kidney stones, asthma, heart problems, or systemic lupus erythematosus. Be careful with Benazeplus if you have elevated blood acid, low folic acid levels, or electrolyte problems, or are dehydrated. Be careful with Benazeplus if you take potassium-sparing diuretics (eg, spironolactone), potassium supplements, or salt substitutes containing potassium because high blood potassium levels may occur and cause listlessness, confusion, abnormal skin sensations of the arms and legs, heaviness of limbs, slowed heart rate, irregular heart rhythm, or stopping of the heart; cholestyramine or colestipol because they may decrease Benazeplus 's effectiveness; nonsteroidal anti-inflammatory drugs (NSAIDs) (eg, indomethacin) because they may decrease Benazeplus 's effectiveness and risk of kidney problems may be increased; barbiturates (eg, phenobarbital), certain chemotherapy medicines, corticosteroids (eg, prednisone), digoxin, dofetilide, ketanserin, narcotic pain medicines (eg, codeine), or medicines for high blood pressure because the risk of their side effects may be increased by Benazeplus; diazoxide, lithium, or nondepolarizing neuromuscular blockers (eg, pancuronium) because their actions and the risk of their side effects may be increased by Benazeplus; angiotensin-converting enzyme (ACE) inhibitors (eg, enalapril) because the risk of high blood potassium and kidney problems may be increased by Benazeplus; diabetes medicines (eg, glipizide) or insulin because their effectiveness may be decreased by Benazeplus. Do not stop taking Benazeplus suddenly.

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CB and o-DCB concentrations which gave the best adapted biomass productivity were determined and found to be 150 and 30 microl l(-1), respectively. The 15 patients were treated by VLAP for benign prostatic hyperplasia. We found that during the period 2003-2007, the highest ASRs for PLC were observed in some Asian populations, ranging from 19.0 to 26.7 per 100,000 in males and 4.8 to 8.7 per 100,000 in females. Further information on learning effects is needed, as is commercially available progression software for Matrix. Glucose potentiates interleukin-1 beta (IL-1 beta)-induced p38 mitogen-activated protein kinase activity in rat pancreatic islets of Langerhans. We address signaling and transcriptional events resulting in peroxisome proliferation, and focus on novel findings concerning the key division components and their interplay. Experienced researchers and clinicians from various specialties were included in the group. The microdeletion of 5q14.3 was the cause of infantile spasm in the patient. A computerized patient database covering all ambulatory visits and hospital admissions at all care facilities in the county of Stockholm, Sweden, was used.

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Study-specific odds ratios (OR) were calculated and combined using random-effects model. CPT and PE were equally efficacious and improvements persist over LTFU, yet, neither produced remission of sleep disturbance. The intense selection underlying these changes was achieved through extensive use of artificial insemination (AI), which also increased consanguinity of the population to a few superior Jersey bulls. We incorporated possible confounders, including weather and long-term and seasonal mortality trends. Associating such a disturbance with each individual transition point in the profile, we obtain a computationally efficient refinement of the thin-element approximation for the analysis and design of diffractive elements in the nonparaxial domain. These results revealed a lack of association between adipokine levels and systemic inflammation with cancer cachexia. The developed method has been verified using the experimental data for inulinase from Kluyveromyces marxianus. The nucleotide exchange factors Grp170 and Sil1 induce cholera toxin release para que sirve el norvasc 10 mg from BiP to enable retrotranslocation. The pattern of skeletal change was favorable both during treatment and in later years.

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