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Adelphan (Amiloride)
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Adelphan

Adelphan is a diuretic. It helps you make more urine and to lose salt and excess water from your body. It helps treat high blood pressure and swelling from heart disease. It also helps treat low potassium levels.

Other names for this medication:
Acortiz, Aldoril, Bisoplus, Cilazil, Clorana, Dehydratin, Dichlotride, Diclotride, Disothiazide, Ditenside, Diunorm, Diurace, Duopril, Dytenzide, Enaplus, Esidrix, Fosinopril, Fozide, Foziretic, Gentipress, Hexazide, Hidroclorotiazida, Hydrex, Hydromet, Hydrozide, Inderide, Lisiplus, Lorzaar, Maxsoten, Medozide, Nefrix, Oretic, Prestole, Propra, Renezide, Sectrazide

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Also known as: Amiloride

Description

Hydrochlorothiazide is a thiazide diuretic (water pill) that helps prevent your body from absorbing too much salt, which can cause fluid retention.

Amiloride is a potassium sparing-diuretic that also prevents your body from absorbing too much salt and keeps your potassium levels from getting too low.

The combination of hydrochlorothiazide and amiloride is used to treat fluid retention (edema) and high blood pressure (hypertension).

Dosage

Take Adelphan by mouth with food. Adelphan 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 Adelphan suddenly.

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. 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 Adelphan 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

Drinking alcohol can increase certain side effects of hydrochlorothiazide and amiloride.

Do not use salt substitutes or low-sodium milk products that contain potassium. These products could cause your potassium levels to get too high while you are taking Adelphan 5-50.

Avoid a diet high in salt. Too much salt will cause your body to retain water and can make this medication less effective.

This medication may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert.

Avoid becoming overheated or dehydrated during exercise and in hot weather. Follow your doctor's instructions about the type and amount of liquids you should drink. In some cases, drinking too much liquid can be as unsafe as not drinking enough.

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Risk assessment of local dermal effects and skin sensitisation under the EU Chemicals Regulation REACH: a proposal for a qualitative, exposure scenario specific, approach. The PROSTALAC implant allows patients to have reasonable function and quality of life during the interim treatment for deep joint infection. The VH and VL genes were subcloned into p gamma 1-Expr and p kappa-Expr respectively, then transfected into XL2-Blue. Use of immune modulation by human adipose-derived mesenchymal stem cells to treat experimental arthritis in mice. Eight trials provided very limited data on the value of carbamazepine as an adjunct to antipsychotics. Detection of statistical asymmetries in non-stationary sign time series: Analysis of foreign exchange data. The footprint of marginal agriculture in the Mediterranean mountain landscape: An analysis of the Central Spanish Pyrenees. The treatment of diabetes insipidus depends on many factors, including the clinical setting, degree and pathophysiologic classification, ability of the patient to compensate for free water losses, and expected duration of the abnormality. Some factors that could potentially influence ANP have been identified, but these and other avenues of investigation warrant further study. Free radicals and other reactive oxygen or nitrogen species are constantly generated in vivo and can cause oxidative damage to DNA.

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Consistently, LF inhibited IFNgamma-induced STAT1 binding to DNA. Beyond crosswalks: reliability of exposure assessment following automated coding of free-text job descriptions for occupational epidemiology. Results of this study demonstrated that defence compounds of Ulomoides dermestoides reduced cell viability and induced DNA damage. A Dense Grid of Reference Iodine Lines for Optical Frequency Calibration in the Range 595-655 nm. Nanoparticles endowed with targeting abilities offer a novel approach for site-specific delivery of chemotherapeutic agents. This reaction furnishes 3-arylated succinimide derivatives in good yields with excellent selectivity. A significant link was found between aerobic colony counts and ATP measurements.

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Sorption mechanism of enrofloxacin on humic acids extracted xanax from Brazilian soils. The suitability of neutralized perfluorosulphonic acid (Nafion) as a surface for the attachment and growth of human cells was investigated in tissue culture. Malalignment of the lower extremity is commonly seen in patients with severe osteoarthritis undergoing total knee arthroplasty (TKA) and is believed to play a role in quadriceps strength loss. MR imaging allows the guidance and the follow-up of cryolesions of the liver with good accuracy. Comparisons were made between the pre-AIDS and the AIDS death groups by logistic regression for: age, location of residence at death, year of death and risk exposure. Enzyme immunoassay for antibodies in serum using a covalent chromatographic method for separation of the bound label. The antisense RNA fragment produced a similar effect, but in neither case was readthrough of UAA or UAG observed. Although well-conducted and reported randomised trials are still needed to inform practice (no trial data exists reporting hospital and services outcomes, satisfaction with care and economics) pipothiazine palmitate is a viable choice for clinician and recipient of care. Cilengitide 2000 mg was considered safe and was selected for the subsequent randomised phase II part assessing progression-free survival. RPE cells generated tractional forces in response to IGF-I and -II with IGF-I being the more potent stimulus.

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