The KINERET logo and generic name (anakinra)

KINERET Support Program

Peggy's symptoms began at a busy time in her life.

"I had Megan, my youngest child in 1988 and started my masters's degree in 1990. My symptoms started in 1993, the day before Megan's fifth birthday. I started to get really achy, almost flu-like. I got up in the morning with difficulty moving anything."—Peggy, RA patient

Woman baking with her grandkids

As a caretaker, it was difficult for her to be the one who needed care.

"I wasn't a complainer, but people could see that I was suffering. My mother came down a lot of the time because my kids were little. Other moms would take my sons to hockey and my daughter to dance classes. While I appreciated everyone's help, part of me was a little resentful. I wasn't able to be the mother I wanted to be and other people had to step in."—Peggy, RA patient

For years, doctors were unable to find a treatment that worked for Peggy.

"I had gone to multiple doctors who were unable to give me a diagnosis. I tried many different treatments to get my symptoms under control, but many of them didn’t work for me and I had a hard time tolerating them."—Peggy, RA patient

Woman enjoying being outside with her husband

Her rheumatologist was unwilling to give up.

"With multiple therapeutic failures, my rheumatologist continued her search for a treatment. She attended a rheumatology conference and with me and my RA diagnosis in mind, she came back and said 'I have something for you.'"—Peggy, RA patient

Peggy experienced a reduction in her symptoms after starting KINERET.

"The fatigue and the aching in my joints started to improve."—Peggy, RA patient

Female physician talking to a nurse

Today, Peggy continues to care for others.
But she also takes time for herself.

"I still work part time, but I try to be home by six o'clock because I know my body will require some rest."—Peggy, RA patient

INDICATIONS

What is KINERET (anakinra)?

KINERET is a prescription medicine called an interleukin-1 receptor antagonist (IL-1Ra) used to:

  • Reduce signs and symptoms and slow the damage of moderate to severe active rheumatoid arthritis (RA) inadults when one or more other drugs for RA have not worked
  • Treat people with a form of Cryopyrin-Associated Periodic Syndromes (CAPS) called Neonatal-OnsetMultisystem Inflammatory Disease (NOMID)
  • Treat people with Deficiency of Interleukin-1 Receptor Antagonist (DIRA)

Kineret is not for children with Juvenile Rheumatoid Arthritis.

IMPORTANT SAFETY INFORMATION

Who should not receive KINERET?

You should not receive KINERET if you are allergic to proteins made from bacteria called E. coli or any of the ingredients in KINERET.

What should I tell my healthcare provider before taking KINERET?

You should tell your doctor if you:

  • Have an infection, a history of infections that keep coming back, or other problems that can increase your risk of infections.
  • Are scheduled to receive any vaccines since people using KINERET should not receive live vaccines.
  • Have kidney problems.
  • Are pregnant, planning to become pregnant, or breastfeeding. It is not known if KINERET will harm your unborn baby or passes into your breastmilk. You and your healthcare provider should decide if you will use KINERET or breastfeed.

What are the serious side effects of KINERET?

KINERET can lead to serious infections, including tuberculosis (TB). Because KINERET is a medicine that affects your immune system and may lower your risk to fight infection, your doctor may test for TB and treat new or unknown TB, before you start taking KINERET.

You Should Know: Signs and symptoms of a serious infection could include fever, chills, or excessive sweating, open sores on your body, nausea, lightheadedness, or vomiting, dizziness or lightheadedness.

You should tell your healthcare provider or get medical help if new symptoms of an infection appear. They can be life-threatening or cause death.

You should stop using KINERET and call your healthcare provider or get emergency help right away if you have any of these symptoms of an allergic reaction: swelling of your face, lips, mouth, or tongue; trouble breathing; wheezing; severe itching; skin rash, redness, or swelling outside of the injection site area; dizziness or fainting; fast heartbeat or pounding in your chest (tachycardia); or sweating. People with DIRA may have an increased risk of allergic reactions, especially in the first several weeks.

It is not known if treatment with medicines that cause immunosuppression, like KINERET, affect your risk of getting cancer.

KINERET may cause you to have a lower number of certain white cells (neutrophils). Neutrophils are important in fighting infections. You should have blood tests before starting treatment with KINERET, then monthly for 3 months. After the first 3 months you should have your blood tested every 3 months for up to 1 year.

Before taking KINERET, you should tell your healthcare provider about all your medical conditions and medicines including prescription and over-the-counter medicines, vitamins, supplements, and herbal remedies.

What are other possible side effects of KINERET?

The most common side effects of KINERET include injection site skin reactions, worsening RA (if you already have RA), headache, nausea and vomiting, diarrhea, joint pain, fever, general feeling of discomfort, sore throat or runny nose, sinus infection, and pain in your stomach area.

You Should Know: These are not all the possible side effects for KINERET. For more information, ask your healthcare provider or review the Prescribing Information for KINERET at https://www.kineretrx.com/pdf/Full-Prescribing-Information-English.pdf.

If you suspect that you have experienced a side effect, call your healthcare provider. You may also report them to the US Food and Drug Administration (FDA) at 1-800-FDA-1088.

You Should Know: These are not all the possible side effects for KINERET. For more information, ask your healthcare provider or review the Prescribing Information for KINERET at https://www.kineretrx.com/pdf/Full-Prescribing-Information-English.pdf.

If you suspect that you have experienced a side effect, call your healthcare provider. You may also report them to the US Food and Drug Administration (FDA) at 1-800-FDA-1088.