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Acortiz (Amiloride)
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Acortiz

Acortiz is a medication typically used with other medications to treat high blood pressure or swelling due to heart failure or cirrhosis of the liver. Acortiz is classified as a potassium-sparing diuretic.

Other names for this medication:
Acuren, Amiloretic, Amiloride, Bisoplus, Bpzide, Cosaar, Ditenside, Dociteren, Elektra, Enaplus, Eprosartan, Eprotan, Fosicomp, Foziretic, Hidroclorotiazida, Hydrex, Lisiplus, Lispirl, Lodoz, Monopril, Prestole, Ridaq, Selokomb, Tandiur, Tevanap, Tevetec, Timolide, Triamtereen

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

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To determine whether protein tyrosine phosphatase 1B (PTP1B) is expressed in rat retinal pigment epithelium (RPE) cells, to evaluate whether inhibition of PTP1B contributes to initiation of RPE cells into an active state, and to investigate the signaling pathways involved in this process. This article provides the reader with an overview of copper storage disorders in humans and animals. Histopathological examination showed a dermal chronic granulomatous infiltrate with fungal hyphae and yeast forms suggestive of Basidiobolus ranarum. This suggests that accumulated PrP(Sc), or perhaps fibrillar complexes formed of prion only inhibit SNARE complexes that are formed ex vivo following biochemical extraction. CYP11a (tttta)(n) repeat-polymorphism genotype and serum ovarian and adrenal androgen levels. The Immuknow assay may be of help in evaluating the immune response of transplanted patients. A phase I study of temsirolimus plus carboplatin plus paclitaxel for patients with recurrent or metastatic (R/M) head and neck squamous cell cancer (HNSCC). A Phase II trial was conducted to determine the activity and toxicity of flavopiridol in untreated patients with metastatic NSCLC. Hemiballism-hemichorea and posterior communicating artery stenosis. Refractive state and corneal curvature were measured by IR photoretinoscopy and IR keratometry respectively.

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Plasticity of risky decision making among maltreated adolescents: Evidence from a randomized controlled trial. To address this, we propose a novel multi-view outlier detection method with a consensus regularization on the latent representations. Out of sight but not out of mind: alternative means of communication in plants. Longitudinal shape irregularity of airway lumen assessed by CT in patients with bronchial asthma and COPD. Current ongoing genome-wide association (GWA) studies represent a powerful approach to uncover common unknown genetic variants causing common complex diseases. Chemotherapy may yield only short-term responses, whereas immunotherapy appears to yield durable complete responses in a subset neurontin medication cost of patients. Overexpression of microRNA-722 fine-tunes neutrophilic inflammation by inhibiting Rac2 in zebrafish.

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