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V Lim Rheumatology Department,
Nottingham City Hospital, Nottingham NG5 1PB Correspondence to: V Lim vunroei{at}hotmail.com
Leflunomide (Arava; Aventis Pharma) is used widely
to treat inflammatory arthritis. We report a case of a probable
interaction between leflunomide and warfarin.
A 49 year old man with resistant rheumatoid arthritis started taking
leflunomide at the recommended loading dose of 100 mg daily for three
days. His international normalised ratio had been stable for a year
while he was taking warfarin, and two days before starting treatment
with leflunomide it was 3.4. After he took the second dose of
leflunomide, he developed gross haematuria, for which he required
hospital admission. His international normalised ratio had risen to 11, and warfarin was discontinued. His haemoglobin concentration was
satisfactory and the haematuria spontaneously resolved several hours
after admission. His ratio remained raised for the next two days, even
though he had stopped taking warfarin, and he was given 1 mg of vitamin
K intravenously on the third day. Twelve hours later, the ratio
decreased to 1.9 (figure), which coincided with the change to the
leflunomide maintenance dose of 20 mg daily. Subsequently he began
taking warfarin again but at a lower dose of 1 mg daily, which was
sufficient to maintain his international normalised ratio within the
recommended range.
Leflunomide was considered to have caused the increase in the
patient's international normalised ratio. Such a role for leflunomide is supported by the temporal relation to the abnormal ratio and the
subsequent lower warfarin doses required to maintain the ratio within
the normal range. A rechallenge was not possible or ethical.
Leflunomide is rapidly converted to the active metabolite A771726 by
first pass metabolism in the gut wall and liver. A771726 inhibits
cytochrome P-4502C9 and can increase the bioavailability of
drugs metabolised by cytochrome P-4502C9, such as warfarin and phenytoin. This is important as many patients with inflammatory arthritis also take warfarin. The interaction between leflunomide and
warfarin was not detected in clinical trials
1 2
nor is it
mentioned in the British National Formulary.3
We found no published reports of an interaction between leflunomide and
warfarin.

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International normalised ratio (INR) in relation to leflunomide
treatment
The first information booklet for healthcare professionals on
leflunomide4 implied that it was metabolised by cytochrome P-4502C9 and its effects may be increased, rather than
decreased, by warfarin. This was contrary to the pharmacokinetics,
according to the summary of product characteristics for
Arava.5 We informed our hospital drug information
department, the Committee on Safety of Medicines, and Aventis Pharma.
The Committee on Safety of Medicines had received over 300 reports of
raised international normalised ratio in patients taking leflunomide
concurrently with warfarin. Aventis Pharma has released CD Roms
(Information for professionals and Information for
patients), which contain the correct drug information.
Footnotes
Funding: None.
Competing interests: None declared.
References
| 1. | Mladenovic V, Domljian Z, Rozman B, Jajic I, Mihajlovic D, Dordevis J, et al. Safety and effectiveness of leflunomide in the treatment of patients with active rheumatoid arthritis: results of a randomised, placebo-controlled, phase II study. Arthritis Rheum 1995; 38: 1595-1603[Web of Science][Medline]. |
| 2. | Blaz Rozman, for the Leflunomide Investigators' Group. Clinical experience with leflunomide in rheumatoid arthritis. J Rheumatol 1998; 25(suppl 53): 27-32S. |
| 3. | British Medical Association, Royal Pharmaceutical Society of Great Britain. British national formulary. London: BMA, RPS, March, 2001 (No 41). |
| 4. |
Leflunomide information booklet for healthcare professionals questions and answers.
Uxbridge: Hoechst Marion Roussel, 1999.
|
| 5. | Summary of product characteristics for Arava. Uxbridge: Hoechst Marion Roussel, 1999. |
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