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Iperton (Amiloride)
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Iperton

Iperton is a pyrizine compound used to treat hypertension and congestive heart failure. For use as adjunctive treatment with thiazide diuretics or other kaliuretic-diuretic agents in congestive heart failure or hypertension.

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Acortiz, Acuren, Adelphan, Angiozide, Aquazide, Briazide, Cibadrex, Clorana, Condiuren, Cosaar, Coteveten, Crinoretic, Dehydratin, Ditenside, Dithiazide, Duopril, Emcoretic, Enaplus, Epratenz, Eprosartan, Esidrex, Hexazide, Hypothiazid, Inderide, Iperton, Lispirl, Monozide, Olina, Quinaplus, Ridaq, Tandiur, Tevanap, Timolide, Turfa, Zofenilduo

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Also known as: Amiloride

Description

Iperton 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 Iperton is Iperton.

Dosage

Take Iperton by mouth with food. Iperton 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 Iperton suddenly.

Overdose

If you overdose Iperton 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 Iperton 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 Iperton if you are allergic to Iperton components or to any ingredient in Iperton or any other sulfonamide (eg, sulfamethoxazole). Be careful with Iperton if you're pregnant or you plan to have a baby, or you are a nursing mother. Be careful with Iperton if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement. Be careful with Iperton if you have allergies to medicines, foods, or other substances. Be careful with Iperton if you have cirrhosis or liver problems, diabetes, gout, kidney problems or kidney stones, asthma, heart problems, or systemic lupus erythematosus. Be careful with Iperton if you have elevated blood acid, low folic acid levels, or electrolyte problems, or are dehydrated. Be careful with Iperton 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 Iperton 's effectiveness; nonsteroidal anti-inflammatory drugs (NSAIDs) (eg, indomethacin) because they may decrease Iperton '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 Iperton; diazoxide, lithium, or nondepolarizing neuromuscular blockers (eg, pancuronium) because their actions and the risk of their side effects may be increased by Iperton; angiotensin-converting enzyme (ACE) inhibitors (eg, enalapril) because the risk of high blood potassium and kidney problems may be increased by Iperton; diabetes medicines (eg, glipizide) or insulin because their effectiveness may be decreased by Iperton. Do not stop taking Iperton suddenly.

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Randomized controlled trials (RCTs) comparing maternal and neonatal outcomes following prophylactic antibiotics administered prior to skin incision versus after neonatal cord clamping during cesarean delivery. Dental enamel matrix--isolation and partial sequence of a peptide component. Use of Peptide-Based Enzyme-Linked Immunosorbent Assay followed by Immunofluorescence Assay To Document Ehrlichia chaffeensis as a Cause of Febrile Illness in Nicaragua. Percent decreases in skinfold thickness for ultrarunners was lower than the percent decreases in skinfold thickness reported for ultraswimmers and ultracyclists. Rat enamelin was completely removed from maturation-stage enamel without any accumulation of 32-kDa enamelin. Information about drowning accidents in 2010 and 2011 was collected using two methods. The purpose of this systematic review was to describe and examine the current use of treatment summaries and survivorship care plans ( side effects of lopressor 50 mg TSs/SCPs) for cancer survivors, as well as to summarize and critically assess relevant literature regarding their preferences and usefulness. This paper summarizes some recent findings on the physiopathology of facial pain.

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Laxative effects of Liriope platyphylla are tightly correlated with suppression of endoplasmic reticulum stress in loperamide-induced constipation of SD rats. Alpha 1-antitrypsin content of blood serum in chronic lung diseases. A custom video analysis system was used to assess dynamic ND during treadmill walking. Rhythm Control and AV Node Ablation in CRT Patients with Atrial Fibrillation: Should They be Performed Together or Alternatively?. The short- and long-term fates of memory items retained outside the focus of attention. Technical possibility of the movable attachment of models in articulators. Healthy adults in each study were randomised to one of four training conditions: two stimulus-congruent conditions, where same faces were used during all phases of the task, and two stimulus-incongruent conditions, where faces of the opposite sex (Experiment 1) or faces depicting another emotion (Experiment 2) were used after the modification phase.

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