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Since the drug trials, thebody.

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Ezetimibe tablets should be used during pregnancy only if the potential benefit to the mother justifies the risk to the fetus.

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Patients in the trial had LDL levels of about 320 milligrams per deciliter at the beginning of the trial, about three times the level cardiologists deem acceptable.

When I see doctors, they treat me like I'm nuts, they don't see anything on film or other scans.

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To put it differently generics have identical active ingredients and their pharmacological effects are the same, as those of their brand-name equivalents.

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The results of the Enhance study were described as “shocking” by Dr.

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If you're not overweight, don't smoke, eat reasonably well, and are physically active, the medical establishment may have very little to offer you.

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The extended-release formulation, Toprol-XL, was approved in 1992 and was given once daily, making it far more patient friendly.

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NOT take another dose and try to move on to the next option to lower cholesterol.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program using the contact information at the bottom of this page.

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What was the “cure” for things years ago when there were no Statins.

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Do not take Zetia if you are allergic to it or any of its ingredients.

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Whereas when minerals are delivered in an unbalanced pH body, the body cannot absorb the minerals and use them for the proper health of the body and organs such as the kidneys, bladder, liver, gallbladder and thyroid.

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Cholesterol reducing drugs in high doses have been shown in study after study to reduce cholesterol effectively and reduce the risk of heart attack.

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When ZETIA is co-administered with an HMG-CoA reductase inhibitor, liver function tests should be performed at initiation of therapy and according to the recommendations of the HMG-CoA reductase inhibitor.

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From the start of the trial to the end of Week 33, discontinuations due to an adverse reaction occurred in 7 (6%) patients in the Zetia coadministered with simvastatin group and in 2 (2%) patients in the simvastatin monotherapy group.

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