Stila Cc Color Correcting Broad-spectrum Spf 20 02 Light

Stila Cc Color Correcting Broad-spectrum Spf 20 02 Light Manufacturers

• Stila Styles, Llc
  

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  Stila Cc Color Correcting Broad-spectrum Spf 20 02 Light | Stila Styles, Llc

  

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  apply liberally 15 minutes before sun exposure use a water resistant sunscreen if swimming or sweating reapply at least every 2 hours children under 6 months: Ask a doctor Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: limit time in the sun, especially from 10 a.m.-2 p.m. wear long-sleeved shirts, pants, hats, and sunglasses
  

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• Stila Styles, Llc
  

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  Stila Cc Color Correcting Broad-spectrum Spf 20 02 Light | Breckenridge Pharmaceutical, Inc.

  

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  There is no fixed dosage regimen for the management of type 2 diabetes with Repaglinide Tablets.

  The patient's blood glucose should be monitored periodically to determine the minimum effective dose for the patient; to detect primary failure, i.e., inadequate lowering of blood glucose at the maximum recommended dose of medication; and to detect secondary failure, i.e., loss of an adequate blood glucose-lowering response after an initial period of effectiveness. Glycosylated hemoglobin levels are of value in monitoring the patient's longer term response to therapy.

  Short-term administration of Repaglinide Tablets may be sufficient during periods of transient loss of control in patients usually well controlled on diet.

  Repaglinide Tablet doses are usually taken within 15 minutes of the meal but time may vary from immediately preceding the meal to as long as 30 minutes before the meal.

  Starting Dose

  For patients not previously treated or whose HbA1c is < 8%, the starting dose should be 0.5 mg with each meal. For patients previously treated with blood glucose-lowering drugs and whose HbA1c is ≥ 8%, the initial dose is 1 or 2 mg with each meal preprandially (see previous paragraph).

  Dose Adjustment

  Dosing adjustments should be determined by blood glucose response, usually fasting blood glucose. Postprandial glucose levels testing may be clinically helpful in patients whose pre-meal blood glucose levels are satisfactory but whose overall glycemic control (HbA1c) is inadequate. The preprandial dose should be doubled up to 4 mg with each meal until satisfactory blood glucose response is achieved. At least one week should elapse to assess response after each dose adjustment.

  The recommended dose range is 0.5 mg to 4 mg taken with meals. Repaglinide Tablets may be dosed preprandially 2, 3, or 4 times a day in response to changes in the patient's meal pattern. The maximum recommended daily dose is 16 mg.

  Patient Management

  Long-term efficacy should be monitored by measurement of HbA1c levels approximately every 3 months. Failure to follow an appropriate dosage regimen may precipitate hypoglycemia or hyperglycemia. Patients who do not adhere to their prescribed dietary and drug regimen are more prone to exhibit unsatisfactory response to therapy including hypoglycemia. When hypoglycemia occurs in patients taking a combination of Repaglinide Tablets and a thiazolidinedione or Repaglinide Tablets and metformin, the dose of Repaglinide Tablets should be reduced.

  Patients Receiving Other Oral Hypoglycemic Agents

  When Repaglinide Tablets are used to replace therapy with other oral hypoglycemic agents, Repaglinide Tablets may be started on the day after the final dose is given. Patients should then be observed carefully for hypoglycemia due to potential overlapping of drug effects. When transferred from longer half-life sulfonylurea agents (e.g., chlorpropamide) to repaglinide, close monitoring may be indicated for up to one week or longer.

  Combination Therapy

  If Repaglinide Tablets monotherapy does not result in adequate glycemic control, metformin or a thiazolidinedione may be added. If metformin or thiazolidinedione monotherapy does not provide adequate control, Repaglinide Tablets may be added. The starting dose and dose adjustments for Repaglinide Tablets combination therapy is the same as for Repaglinide Tablets monotherapy. The dose of each drug should be carefully adjusted to determine the minimal dose required to achieve the desired pharmacologic effect. Failure to do so could result in an increase in the incidence of hypoglycemic episodes. Appropriate monitoring of FPG and HbA1c measurements should be used to ensure that the patient is not subjected to excessive drug exposure or increased probability of secondary drug failure.

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