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Keen (levonorgestrelreleasing intrauterine system) New Drug Approval On September 19, 2016, Bayer announced the FDA approval of Keen (levonorgestrelreleasing intrauterine system) for the prevention
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Step 1: Wash your hands thoroughly with soap and water.
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Step 2: Take a comfortable position, such as lying down or squatting.
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Step 3: Open the kyleena levonorgestrel-releasing intrauterine system package.
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Step 4: Hold the system by the blue handle and gently insert the T-shaped device into your uterus through the cervix.
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Step 5: Ensure that the strings attached to the system are hanging down from the cervix into the vagina.
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Step 6: Check the correct placement of the system by feeling the strings. They should be approximately 1-2 inches into the vagina.
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Step 7: Trim the strings if they are too long, leaving about 1-2 inches hanging out of the vagina.

Who needs kyleena levonorgestrel-releasing intrauterine system?

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Kyleena levonorgestrel-releasing intrauterine system is suitable for women who want long-term contraception.
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It is also recommended for women who have already had a child and want effective birth control that can last up to 5 years.
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Women who have heavy or painful periods may benefit from using Kyleena, as it can help reduce symptoms.
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Kyleena levonorgestrel-releasing intrauterine system is a form of birth control that is inserted into the uterus to prevent pregnancy.
Kyleena levonorgestrel-releasing intrauterine system is typically prescribed by a healthcare provider and is not required to be filed by the individual receiving the device.
Kyleena levonorgestrel-releasing intrauterine system is inserted by a healthcare provider during a simple in-office procedure.
The purpose of kyleena levonorgestrel-releasing intrauterine system is to provide long-term reversible contraception.
The healthcare provider may report information such as the date of insertion, any side effects experienced, and the date of removal if applicable.
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