Iclevia
Generic: Levonorgestrel And Ethinyl Estradiol
Combined oral contraceptive✓ FDA-verified
View full FDA label ↗Iclevia is a medication used by women to prevent pregnancy. It works by stopping the ovaries from releasing eggs. You take it as a tablet, one each day for 91 days, starting with a white tablet and then taking a green tablet for the last 7 days. It's important to know that Iclevia should not be used by women who smoke and are over 35 years old due to an increased risk of serious blood clots. Additionally, if you are taking certain hepatitis C medications that include ombitasvir, paritaprevir, or ritonavir, you should not use this medication.
✦
Uses
- Prevent pregnancy.
◷
Dosage
Take one tablet daily by mouth at the same time for 91 days.
Start on a Sunday after your period begins.
Use additional contraception for the first 7 days if starting new.
Follow the order on the Extended-Cycle Wallet.
Take one green tablet daily for the last 7 days.
Always follow your doctor's specific instructions for your dose.
⚠
Side effects
Common
headachenauseaacnebreast tendernessweight gaindepressioncardiovascular events
Serious
strokeliver disease
🛑
Warnings
⚠ Important warnings
- Do not smoke if over 35 years old.
- Increased risk of serious cardiovascular events.
- Not recommended for lactating women.
- Use caution after second-trimester abortion or miscarriage.
⇄
Drug interactions
- Enzyme inducersmay decrease effectivenessCaution
- Colesevelamdecreases exposure to ethinyl estradiolCaution
- Atorvastatinincreases estrogen exposureMonitor
- Grapefruit juicemay increase estrogen exposure.Caution
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Answers pulled from the FDA label only.
Medical Disclaimer: This content is provided for informational and educational purposes only and is not intended as medical advice. Always consult a qualified healthcare provider before taking any medication.
Data Source: Publicly available drug labeling information from the U.S. Food and Drug Administration (FDA).
Data Source: Publicly available drug labeling information from the U.S. Food and Drug Administration (FDA).
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