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FDA Adds Vitamin B6 and Seizure Warning to Carbidopa/Levodopa Treatments

Written by Ted Samson
Posted on April 24, 2026

Medication pills and bottleThe U.S. Food and Drug Administration (FDA) now requires medications containing carbidopa/levodopa to include a warning about the risk of vitamin B6 deficiency and related seizures.

These medications are commonly used to treat Parkinson’s disease. The new warning doesn’t mean the treatment works differently. It points out a risk that people with Parkinson’s and their caregivers should know about.

Research has linked carbidopa/levodopa treatment with low vitamin B6 levels in some people with Parkinson’s.

Share your thoughts.

🗳️ Have you had your vitamin B6 levels checked in the past year?
Yes, I was tested, and they found a B6 deficiency.
Yes, I was tested, and my vitamin B6 levels were in the normal range.
No, I haven’t been tested in the past year.

A 2023 study found low B6 levels in nearly 45 percent of people using carbidopa/levodopa intestinal gel and 30 percent of those taking oral carbidopa/levodopa.

What Is Vitamin B6?

Vitamin B6 and supplement bottleVitamin B6 helps your body carry out many important functions, including supporting brain health, making neurotransmitters (chemical messengers), and forming red blood cells.

Carbidopa/levodopa can lower vitamin B6 levels in two ways:

  • The body uses vitamin B6 to process levodopa.
  • Carbidopa may attach to vitamin B6 and make it less active.

Over time, especially at higher doses, this may lead to a deficiency.

Signs and Risks of Vitamin B6 Deficiency

Low vitamin B6 levels can affect the nervous system and other parts of the body. Symptoms may include:

  • Numbness, tingling, or nerve pain
  • Muscle weakness
  • Depression or confusion
  • Fatigue (extreme tiredness)
  • Anemia (low levels of healthy red blood cells)
  • Skin or mouth inflammation

In more severe cases, vitamin B6 deficiency can lead to seizures. In some reported cases linked to carbidopa/levodopa, seizures improved after people received vitamin B6.

What the FDA Found

The warning is based on a review of 14 reported cases of vitamin B6 deficiency-related seizures in people taking carbidopa/levodopa. The FDA noted three patterns:

  • All 14 cases involved higher doses, more than 1,000 milligrams per day.
  • Seizures developed months to years after starting treatment.
  • The seizures stopped after people received vitamin B6.

Although these cases appear to be uncommon, the FDA found enough evidence to require updated safety labeling.

What This Means for People With Parkinson’s

Doctor consultation and patient care

Carbidopa/levodopa remains an effective treatment for Parkinson’s. The new warning is about watching for a rare but important risk. It does not mean people should stop treatment.

The FDA says healthcare providers should check vitamin B6 levels before and during treatment and consider supplements if levels are low.

Let your doctor know if you notice new symptoms such as numbness, tingling, mood changes, or seizures. Low vitamin B6 can cause symptoms, but those symptoms can also have other causes.

Get medical help right away if you or your loved one has a seizure. If you take carbidopa/levodopa, don’t stop or change your dose on your own. Ask your doctor whether vitamin B6 testing or supplements may be right for you.

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On MyParkinsonsTeam, people share their experiences with Parkinson's disease, get advice, and find support from others who understand.

Have you or a loved one had low vitamin B6 levels? Let others know in the comments below.

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