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Andinx (Atenolol)

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Andinx is a beta-blocker that affects the heart and circulation (blood flow through arteries and veins). Andinx is used to treat angina (chest pain) and hypertension (high blood pressure).

Other names for this medication:
Adbeta, Adpine, Agloten, Amlibon, Amlobet, Amlocal, Amlocas, Amlokos, Amlonova, Amlosac, Amlotec, Amlovas, Amnol, Ampin, Amsar, Atbeta, Atekind, Atemarc, Atenolol, Atormin, Atzee, Beten, Camcard, Cardipin, Cardpin, Celbeta, Dilcare, Odinol, Olate, Opime, Samstar, Tenocab, Tensimin, Vascodil

Similar Products:
Sovaldi, Cardizem, Clarinex, Xalatan, Zyvox, Starlix

Also known as: Atenolol


Andinx is created by pharmacy specialists to combat angina, heart attack, high blood pressure, anxiety attacks and migraine. Target of Andinx is to influence circulation. Andinx is also known as Atenolol, Hipres, Atendol, Altol, Atelol, Antipressan, Atenix, Ateno, Betacard, Blokium, Catenol, Corotenol, Notenol, Oraday. Andinx acts as an anti-angina remedy. Andinx operates by controlling and decreasing the strength of heart contractions and, thus, influencing circulation. Andinx is a beta-blocker. You can use Andinx with other anti-high blood pressure medication. Generic name of Andinx is Atenolol. Brand name of Andinx is Andinx.


Usual Adult Dose of Andinx for Hypertension:

Initial dose: 50 mg orally once a day Maintenance dose: 50 to 100 mg orally once a day Maximum dose: 100 mg per day Comments: -If desired response not achieved after 1 to 2 weeks, increase to 100 mg may be beneficial. -Doses greater than 100 mg once a day did not result in significant additional antihypertensive effects. Use: For the treatment of hypertension alone or in combination with other antihypertensive agents.

Usual Adult Dose of Andinx for Angina Pectoris Prophylaxis:

Initial dose: 50 mg orally once a day -Increase to 100 mg orally once a day after 1 week if optimal response not achieved Maintenance dose: 50 to 200 mg orally once a day Maximum dose: 200 mg per day Comments: -Some patients may require 200 mg per day to attain optimal effect. Use: For the long-term management of angina pectoris due to coronary atherosclerosis.

Usual Adult Dose for Angina Pectoris:

Initial dose: 50 mg orally once a day -Increase to 100 mg orally once a day after 1 week if optimal response not achieved Maintenance dose: 50 to 200 mg orally once a day Maximum dose: 200 mg per day Comments: -Some patients may require 200 mg per day to attain optimal effect. Use: For the long-term management of angina pectoris due to coronary atherosclerosis.

Usual Adult Dose of Andinx for Myocardial Infarction:

50 mg orally twice a day or 100 mg orally once a day Comments: -If IV beta blockers are contraindicated or inappropriate, oral therapy should continue for at least 7 days post-myocardial infarction (MI). -Treatment with beta blockers post MI should generally continue for 1 to 3 years if there are no contraindications. Use: For the management of hemodynamically stable patients with definite or suspected acute myocardial infarction to reduce cardiovascular mortality.

Usual Geriatric Dose for Hypertension:

Initial dose: Consider reducing the starting dose to 25 mg orally once a day

Detailed Andinx dosage information


Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

Overdose symptoms may include extreme weakness or lack of energy, very slow heart rate, shortness of breath, or fainting.


Store at room temperature between 20 and 25 degrees C (68 and 77 degrees F) away from moisture and heat. Keep container tightly closed. 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 Andinx are:

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Age Is the Only Predictor of Poor Bowel Preparation in the Hospitalized Patient. This new conceptualization has integrated information acceptance, health service utilization, and information behavior theories. Although it is well known that addiction is associated with adverse medical consequences, the effects of the spectrum of unhealthy drug use (illicit drug or prescription misuse) on chronic conditions such as hypertension and diabetes are understudied. A surface plasmon resonance assay showed clear interaction between human PQBP-1 and Q(11), representative of the poly-Q tract of the ataxin-1 of Old World monkeys. Using detergent-resistant membrane (DRM) assays, as well as transmembrane (TM) interactions and ganglioside GM1 binding, we present evidence supporting the localization of podoplanin in raft platforms important for cell signalling. For this purpose, the thermal effects connected with solvent adsorption on the series of octadecyl stationary-bonded phases were investigated. Tumour biology of colorectal liver metastasis is a more important factor in survival than surgical margin clearance in the era of modern zyrtec 10 mg make you sleepy chemotherapy regimens. We report the long-term safety and efficacy of daclizumab 150 mg subcutaneous every 4 weeks in patients with RRMS in the SELECTED open-label extension study.

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The aggregation of polyglutamine containing protein sequences is implicated in a family of familial neurodegenerative diseases, the expanded CAG repeat diseases. Ordered mesoporous silica (OMS) materials are considered a promising drug delivery system for the dissolution enhancement of poorly soluble compounds. Determination of labile inorganic and organic species of Al and Cu in river waters using the diffusive gradients in thin films technique. An optimized, synthetic DNA vaccine encoding the toxin A and toxin B receptor binding domains of Clostridium difficile induces protective antibody responses in vivo. These antagonists have both bronchodilator and anti-inflammatory properties and act simultaneously as beta-adrenoceptor agonists and corticosteroids. Fabrication of chitosan/gallic acid 3D microporous scaffold for tissue engineering applications. We examined whether axon degeneration precedes myelin degeneration or vice versa in SCA1-KI mice and then attempted to mitigate motor neuron degeneration by intrathecally administering mesenchymal stem cells (MSCs). The aim of this retrospective study is to review DFSP cases in order to analyze risk factors for metastasis. Here we summarize the current knowledge about the extra-adrenal GC synthesis in the mucosal tissues, with special emphasis on the intestinal epithelium, and its implication on the regulation of immune homeostasis and inflammatory processes. These findings are consistent with their known functions, and they may help to identify individuals best suited for apoptosis-targeted therapy as a baseline data in gastric carcinoma.

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