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Calock (Atenolol)

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Calock is in a class of medications called beta blockers. It works by relaxing blood vessels and slowing heart rate to improve blood flow and decrease blood pressure. Calock is used alone or in combination with other medications.

Other names for this medication:
Altol, Aminol, Amloact, Amlogen, Amlogla, Amloheart, Amlop, Amlosure, Amodep, Ampilife, Ampine, Atamo, Atecard, Atemarc, Atemos, Atpark, Betatrop, Bibidip, Cardules, Celbeta, Depten, Hipres, Hyten, Intalol, Lonet, Loten, Nalotol, Tenochek, Tenodipin, Tenofed

Similar Products:
Duricef, Dramamine, Precose, Ventolin, Temovate, Requip, Arcoxia, Benicar, Cenforce

Also known as: Atenolol


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


A nurse or other trained health professional will give you this medicine. This medicine is given through a needle placed in one of your veins .

Detailed Calock dosage information


If you overdose Calock and you don't feel good you should visit your doctor or health care provider immediately. Symptoms of Calock are low blood sugar, slow heartbeat, heart failure, slowness, low blood pressure, wheezing.


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 Calock 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.


You should not use Calock if you are allergic to atenolol, or if you have:

a serious heart condition such as "AV block" (second or third degree); very slow heartbeats; or heart failure.

To make sure Calock is safe for you, tell your doctor if you have:

congestive heart failure; coronary artery disease (hardened arteries); asthma, bronchitis, emphysema; diabetes; overactive thyroid; liver or kidney disease; pheochromocytoma (tumor of the adrenal gland); peripheral vascular disease such as Raynaud's syndrome; or allergies (or if you are undergoing allergy treatments or skin-testing).

Using Calock during pregnancy could harm the unborn baby. Tell your doctor if you are pregnant or if you become pregnant while using this medicine.

Atenolol can pass into breast milk and may harm a nursing baby. Tell your doctor if you are breast-feeding a baby.

Calock is not approved for use by anyone younger than 18 years old.

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Global Stroke Belt: Geographic Variation in Stroke Burden Worldwide. Here, we review data on the effects of GnRH agonists on cell proliferation and apoptosis, and put forward hypotheses for investigation to determine whether the GnRH receptor acts as a tumor suppressor in neuroendocrine or epithelial cells. Thromboembolism as the adverse event of combined oral contraceptives in Japan. We report an account of a hyperthyroid patient with a discrepancy between the GFR estimates from cystatin C and creatinine. However, the chicken W chromosome is not enriched for genes with expression in female-specific tissues, providing an intriguing contrast to the acquisition and amplification of genes with testis-specific expression on mammalian Y chromosomes and suggesting that the inheritance of chromosomes solely through females or males can lead to different evolutionary outcomes. Consecutive patients with PAA treated at one institution from January 2006 to March 2014 were reviewed under an Institutional Review Board-approved protocol. We then describe useful approaches to kinship classification, such as parentage analysis and sibship reconstruction, and explain how the combined use of marker systems with biparental and uniparental inheritance, demographic information, likelihood analyses, relatedness coefficients, and estimation of misclassification rates can yield reliable classifications of kinship in groups with complex kin structures. The performance of the proposed set of features are evaluated by various classifiers using data acquired from 44 patients with malignant tumors, and 72 patients with benign tumors.

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