Baycol
Name: Baycol
How should I take Baycol?
Take Baycol exactly as directed by your doctor. If you do not understand these directions, ask your pharmacist, nurse, or doctor to explain them to you.
Take each dose with a full glass of water.Eat a low-fat, low-cholesterol diet. To see beneficial effects from Baycol, avoid fatty, high-cholesterol foods. Follow your doctor's directions.
Your doctor may want to monitor your liver function with blood tests before starting treatment with Baycol, at six and twelve weeks after both the start of your treatment and any increase in dose, and periodically (every 6 months) thereafter. Depending on the results of these tests, your doctor can determine how much monitoring you will require.
Grapefruit and grapefruit juice may interact with Baycol. The interaction could lead to potentially dangerous effects. Discuss the use of grapefruit and grapefruit juice with your doctor. Do not increase or decrease the amount of grapefruit products in your diet without first talking to your doctor.
Do not stop taking Baycol without first talking to your doctor. It may be weeks or months before beneficial effects from this medication are seen.
Store Baycol at room temperature away from moisture and heat.What happens if I miss a dose?
Take the missed dose as soon as you remember. However, if it is almost time for your next dose, skip the missed dose and take only your next regularly scheduled dose. Do not take a double dose of Baycol.
What should I avoid?
Grapefruit and grapefruit juice may interact with Baycol. The interaction could lead to potentially dangerous effects. Discuss the use of grapefruit and grapefruit juice with your doctor. Do not increase or decrease the amount of grapefruit products in your diet without first talking to your doctor.
Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
Some side effects may not be reported. You may report them to the FDA.
Medical Disclaimer
Cerivastatin Pregnancy Warnings
Cerivastatin has been assigned to pregnancy category X by the FDA. Animal studies have revealed evidence of teratogenicity, including an increase in the incidence of skeletal malformations. There are no controlled data in human pregnancy. However, HMG-CoA reductase inhibitors are known to inhibit biosynthetic processes necessary in fetal development. Rare cases of congenital anomalies have been reported following prenatal exposure to other HMG-CoA reductase inhibitors. Cerivastatin use is considered contraindicated during pregnancy.
The VATER association (vertebral anomalies, anal atresia, tracheo-esophageal fistula with esophageal atresia, renal and radial dysplasia) was reported in an infant girl whose mother received lovastatin 10 mg and dextroamphetamine 10 mg daily during the first trimester of pregnancy for the treatment of hypercholesterolemia and progressive weight gain. Both drugs were discontinued five weeks later, at approximately nine weeks gestation, when pregnancy was confirmed.
Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
Medical Disclaimer