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Atorvastatin

Atorvastatin is a statin medication used to prevent cardiovascular disease in those at high risk and to treat abnormal lipid levels. For the prevention of cardiovascular disease, statins are a first-line treatment. It is taken by mouth.

Other names for this medication:
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Description

{name} (atorvastatin) belongs to a group of drugs called HMG CoA reductase inhibitors, or "statins."

{name} is used together with diet to lower blood levels of "bad" cholesterol (low-density lipoprotein, or LDL), to increase levels of "good" cholesterol (high-density lipoprotein, or HDL), and to lower triglycerides (a type of fat in the blood).

{name} is used to treat high cholesterol, and to lower the risk of stroke, heart attack, or other heart complications in people with type 2 diabetes, coronary heart disease, or other risk factors such as genetically high cholesterol.

{name} is for use in adults and children who are at least 10 years old.

Dosage

Generic Atorvastatin can be taken in tablets. You should take it by mouth. It is better to take Generic Atorvastatin once a day at the same time with meals or without it. If you want to achieve most effective results do not stop taking Generic Atorvastatin suddenly.

Overdose

If you overdose Generic Atorvastatin and you don't feel good you should visit your doctor or health care provider immediately.

Storage

Store at room temperature between 20 to 25 degrees C (68 to 77 degrees F) away from moisture and heat. 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 Atorvastatin 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

You should not use Atorvastatin if you are allergic to atorvastatin, or if you have:

liver disease; or if you are pregnant or breastfeeding.

Atorvastatin can harm an unborn baby or cause birth defects. Do not use if you are pregnant. Stop taking Atorvastatin and tell your doctor right away if you become pregnant. Use effective birth control to prevent pregnancy while you are taking this medicine.

Atorvastatin may pass into breast milk and could harm a nursing baby. Do not breastfeed while you are taking Atorvastatin.

To make sure this medicine is safe for you, tell your doctor if you have ever had:

liver problems; muscle pain or weakness; kidney disease; diabetes; a thyroid disorder; or if you drink more than 2 alcoholic beverages daily.

Atorvastatin can cause the breakdown of muscle tissue, which can lead to kidney failure. This happens more often in women, in older adults, or people who have kidney disease or poorly controlled hypothyroidism (underactive thyroid).

Atorvastatin is not approved for use by anyone younger than 10 years old.

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Responsibility attitudes and interpretations are characteristic of obsessive compulsive disorder. In a master equation approach, slow and fast folding speeds are directly correlated to the large and small contributions of the (rate-limiting) slow kinetic modes. To investigate the potential importance of prostaglandins and thromboxane in systemic lupus erythematosus (SLE), the effects of a nonsteroidal antiinflammatory drug (piroxicam) and a thromboxane synthetase inhibitor (dazmegrel) were examined on survival, proteinuria, food consumption, body weight, and peripheral lymphocyte subset distribution in the NZB/W model of autoimmune lupus disease. T-system membranes in microsomal fractions of crayfish muscles: identification and differences in protein composition. Correction: Identifying and quantifying heterogeneity in high content analysis: application of heterogeneity indices to drug discovery. Structural insight into dimeric interaction of the SARAH domains from Mst1 and RASSF family proteins in the apoptosis pathway. This study was performed in patients with metastatic lung tumors who underwent surgery during the 22 years after November 1975 in this department. On the other hand, diltiazem did not have a significant influence on heart rate responses.

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Acute exertional compartment syndrome is an uncommon illness that occurs after a period of strenuous exercise. A first total synthesis of the nucleoside antibiotic herbicidin B (1) was achieved in which a novel aldol-type C-glycosidation reaction promoted by samarium diiodide (SmI2) was used as a key step. Most complications occur early in life, in a silent and progressive way. We reviewed the dossiers of four women developing pruriginous exanthema several hours after infusion. Preparation of human antibodies to TNF-alpha using ribosome display technology. MasR blockade reduced portal pressure, indicating that activation of this receptor in splanchnic vasculature promotes portal inflow to contribute to development of portal hypertension. A variety of benign cyst may occur in and around the ovary and broad ligament and may simulate serous cystadenomas. Hydrodynamic study on the lower urinary tract effect of prostatectomy in patients with benign prostatic what medication can be taken in place of zantac hyperplasia, changes of pre- and postoperative bladder work load, bladder wall contraction velocity, bladder wall tension and urethral resistance. Surgical strategy for aortoesophageal fistula in the endovascular era. Disrupted intestinal structure in a rat model of intermittent hypoxia.

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This study examines mutations at Y380 (homologous to Shaker T449) to investigate whether C-type and U-type inactivation have distinct molecular mechanisms, and whether C-type inactivation can occur at all in KV2.1. Increased placental gene expression of endoglin may result in vascular dysfunction leading to chronic fetal hypoxia, which may induce VEGF-A to stimulate angiogenesis. In clinical studies, concomitant administration of eptifibatide in patients undergoing elective PCI reduced thrombotic complications in the IMPACT-II (Integrilin to Minimize Platelet Aggregation and Prevent Coronary Thrombosis II) and ESPRIT (Enhanced Suppression of the Platelet IIb/IIIa Receptor with Integrilin Therapy) trials. CD-1, C57/BL and Swiss Webster X DBA mouse strains all displayed neurontin 300 mg picture robust time-dependent habituation. Molecular weight dependence of permselectivity to rat small intestinal blood-lymph barrier for exogenous macromolecules absorbed from lumen.

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Protein single-model quality assessment by feature-based probability density functions. These observations are related to the role of the cytoskeleton in the permeability response of the frog bladder epithelium to vasopressin. The antiproliferative and apoptotic effects of ursolic acid in PC-3 and LNCaP cells implicate its potential therapeutic use for the treatment of hormone refractory and androgen-sensitive prostate cancer. Ninety-two percent of people with IBD in Canterbury, New Zealand were recruited. An analysis of atrophy in the medial mammillary nucleus following hippocampal and fornix lesions in humans and nonhuman primates. Sexual dimorphism of the electrosensory system: a quantitative analysis of nerve axons in elavil 50 mg tablet the dorsal anterior lateral line nerve of the blue-spotted Fantail Stingray (Taeniura lymma). The rapprochement subphase of the separation-individuation process. The mutation (an A to C change) causes a substitution of leucine for arginine at position 166 of the PS1 protein and is located adjacent to the transmembrane domain III, where few mutations have been found.

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