Benefits of ACCRUFeR

You deserve a tolerable iron treatment that you can actually stick with

ACCRUFeR® (ferric maltol) is an effective, low-dose treatment for patients with iron deficiency (ID) or iron deficiency anemia (IDA).

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Why ACCRUFeR?

ACCRUFeR was studied in patients with inflammatory bowel disease (Crohn’s disease or ulcerative colitis) and chronic kidney disease (stages 3 or 4). However, it is FDA approved for other adults with ID and IDA as well.

Here are a few reasons why ACCRUFeR may be right for you!

Uniquely formulated with a “maltol shield”

The iron in ACCRUFeR is shielded by a substance called maltol. The “maltol shield” keeps iron protected from the stomach, so it doesn’t break down until it is ready to be absorbed in the small intestine. By limiting the amount of unabsorbed iron in the body, there is a lower risk for intolerable gastrointestinal side effects.

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Unprecedented tolerability

Across studies, fewer than 5% of patients taking ACCRUFeR discontinued treatment because of side effects.*

*Total of 175 patients across studies

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Backed by clinical studies

ACCRUFeR was proven effective in multiple studies over short-term (12 to 16 weeks) and long-term (52 to 64 weeks) periods. Patients on ACCRUFeR experienced significant improvements in their iron levels compared with those on a placebo.

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Just enough iron

Patients take a low 30 mg dose of ACCRUFeR twice per day. With this dosing, patients in clinical studies did not require IV iron intervention, and treatment did not lead to iron overload.

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Iron you’ll actually take

Traditional oral iron supplements were not effective in patients enrolled in two of ACCRUFeR’s clinical trials. About 40% reported intolerable gastrointestinal side effects as the reason they stopped taking their supplement.

In ACCRUFeR's clinical studies, side effects were considered mild to moderate in nature. Some of the most common side effects included:

  • Gas
  • Diarrhea
  • Constipation
  • Discolored feces
  • Abdominal pain
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Give your stomach a break

Fewer than 5% of the individual patients taking ACCRUFeR (out of 175) reported each of the individual GI-related side effects.