lipitor side effects lipitor
These doses lipitor side effects lipitor to 6 times (100 mg/kg) and 22 times (225 mg/kg) the human AUC at 80 mg/day. lipitor side effects lipitor 2. Inclusion in the study required 1) a baseline LDL-C level ≥ 190 mg/dL or 2) a baseline LDL-C level ≥ 160 lipitor side effects lipitor and positive family lipitor side effects lipitor of FH or documented premature cardiovascular disease in a first or second-degree relative. To be sure that Lipitor is helping your condition and is not causing harmful effects, your blood will need to be tested often. In patients lipitor side effects lipitor clarithromycin, itraconazole, or in patients with HIV taking a combination of ritonavir plus saquinavir or lopinavir plus ritonavir, for doses of Lipitor exceeding 20 mg, appropriate clinical assessment is recommended to ensure that the lowest dose necessary of Lipitor is employed . TABLE 4. Cholesterol and triglycerides can clog your blood vessels. Rx Only Manufactured by Pfizer Ireland Pharmaceuticals Dublin, Ireland LAB-0348-4.0 June 2009 PRINCIPAL DISPLAY PANEL LipitorŽ 10 (atorvastatin calcium) tablets 10 mg LipitorŽ 20 (atorvastatin calcium) tablets lipitor side effects lipitor mg LipitorŽ 40 (atorvastatin calcium) tablets 40 mg LipitorŽ 80 (atorvastatin calcium) tablets 80 mg Lipitor atorvastatin calcium tablet, film coated Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 54868-4229 (0071-0157) Route of Administration ORAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ATORVASTATIN CALCIUM (ATORVASTATIN) ATORVASTATIN CALCIUM 40 mg Inactive Ingredients Ingredient Name Strength CALCIUM CARBONATE CANDELILLA WAX CROSCARMELLOSE SODIUM HYDROXYPROPYL CELLULOSE LACTOSE MONOHYDRATE MAGNESIUM STEARATE CELLULOSE, MICROCRYSTALLINE HYPROMELLOSE POLYETHYLENE GLYCOL TALC TITANIUM DIOXIDE POLYSORBATE 80 Product Characteristics Color white Score no score Shape OVAL (elliptical) Size 15mm Flavor Imprint Code PD;157;40 Contains Packaging # NDC Package Description Multilevel Packaging 1 54868-4229-0 30 TABLET In 1 BOTTLE None 2 54868-4229-1 90 TABLET In 1 BOTTLE None 3 54868-4229-2 15 TABLET In 1 BOTTLE None 4 54868-4229-3 45 TABLET In 1 BOTTLE None Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA020702 07/06/2000 Lipitor atorvastatin calcium tablet, film coated Product lipitor side effects lipitor Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 54868-3946 (0071-0156) Route of Administration ORAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ATORVASTATIN CALCIUM (ATORVASTATIN) ATORVASTATIN CALCIUM 20 mg Inactive Ingredients Ingredient Name Strength CALCIUM CARBONATE CANDELILLA WAX CROSCARMELLOSE SODIUM HYDROXYPROPYL CELLULOSE LACTOSE MONOHYDRATE MAGNESIUM STEARATE CELLULOSE, MICROCRYSTALLINE HYPROMELLOSE POLYETHYLENE GLYCOL TALC TITANIUM DIOXIDE POLYSORBATE 80 Product Characteristics Color white Score no score Shape OVAL (elliptical) Size 12mm Flavor Imprint Code PD;156;20 Contains Packaging # NDC Package Description Multilevel Packaging 1 54868-3946-0 30 TABLET In 1 BOTTLE None 2 54868-3946-1 15 TABLET In 1 BOTTLE None 3 54868-3946-2 90 TABLET In 1 BOTTLE None 4 54868-3946-3 60 TABLET In 1 lipitor side effects lipitor None 5 54868-3946-4 45 TABLET In 1 BOTTLE None Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA020702 03/12/2004 Lipitor atorvastatin calcium lipitor side effects lipitor film coated Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 54868-4934 (0071-0158) Route of Administration ORAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ATORVASTATIN CALCIUM (ATORVASTATIN) ATORVASTATIN CALCIUM 80 mg Inactive Ingredients Ingredient Name Strength CALCIUM CARBONATE CANDELILLA WAX CROSCARMELLOSE SODIUM HYDROXYPROPYL CELLULOSE LACTOSE MONOHYDRATE MAGNESIUM STEARATE CELLULOSE, MICROCRYSTALLINE HYPROMELLOSE POLYETHYLENE GLYCOL TALC TITANIUM DIOXIDE POLYSORBATE 80 Product Characteristics Color white Score no score Shape OVAL (elliptical) Size 19mm Flavor Imprint Code PD;158;80 Contains Packaging # NDC Package Description Multilevel Packaging 1 54868-4934-0 30 TABLET In 1 BOTTLE None 2 54868-4934-1 90 TABLET In 1 BOTTLE None Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA lipitor side effects lipitor 01/11/2006 Lipitor atorvastatin calcium tablet, film coated Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 54868-3934 (0071-0155) Route of Administration ORAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ATORVASTATIN CALCIUM (ATORVASTATIN) ATORVASTATIN CALCIUM 10 mg Inactive Ingredients Ingredient Name Strength CALCIUM CARBONATE CANDELILLA WAX CROSCARMELLOSE SODIUM HYDROXYPROPYL CELLULOSE LACTOSE MONOHYDRATE MAGNESIUM STEARATE CELLULOSE, MICROCRYSTALLINE HYPROMELLOSE POLYETHYLENE GLYCOL TALC TITANIUM DIOXIDE POLYSORBATE 80 Product Characteristics Color white Score no score Shape OVAL (elliptical) Size 10mm Flavor Imprint Code PD;155;10 Contains Packaging # NDC Package Description Multilevel Packaging 1 54868-3934-3 10 TABLET In 1 BOTTLE None 2 54868-3934-0 30 TABLET In 1 BOTTLE None 3 54868-3934-4 45 TABLET In 1 BOTTLE None 4 54868-3934-2 60 TABLET In 1 BOTTLE None 5 54868-3934-1 90 TABLET In 1 BOTTLE None Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA020702 05/05/1997 Labeler - Physicians Total Care, Inc (194123980) Revised: 08/2009Physicians Total Care, Inc Lipitor Generic Name: Atorvastatin (a-TOR-va-STAT-in) Brand Name: Lipitor Lipitor is used for: Lowering high cholesterol and triglycerides in certain patients. Your lipitor side effects lipitor may want to do a blood test to check for signs of muscle damage. The mean LDL-C reduction in this study was 18%.
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