The first two weeks brought loose stools and mild nausea. Those symptoms settled after I began taking the tablet after breakfast. By the third month, my hands felt less stiff in the morning.
Arava
Arava is a prescription medicine for adults with active rheumatoid arthritis or psoriatic arthritis. Its active ingredient, leflunomide, is a conventional disease-modifying antirheumatic drug that reduces immune activity involved in joint inflammation.
Description
Arava is a prescription disease-modifying antirheumatic drug containing leflunomide for adults with active rheumatoid arthritis or psoriatic arthritis. The dose is stated on the pack — follow the leaflet. Leflunomide reduces immune-cell activity involved in joint inflammation and can slow structural damage rather than providing only short-term pain relief.
Composition
Arava tablets contain leflunomide, an immunomodulatory medicine in the conventional synthetic DMARD group. DMARD means disease-modifying antirheumatic drug. Unlike a simple analgesic, a DMARD is intended to influence the inflammatory disease process and protect joint function over time.
Leflunomide is used in adult rheumatology for active rheumatoid arthritis and active psoriatic arthritis. Treatment requires regular clinical monitoring because the medicine can affect the liver, blood-cell production, immune response, and pregnancy safety.
The dose is stated on the pack — follow the leaflet. Some treatment plans begin with a loading regimen before the maintenance dose, while others avoid the loading dose when tolerability is a concern.
Dosage and usage
Arava tablets are taken orally, usually once daily. The dose is stated on the pack — follow the leaflet. A loading regimen may be used in some treatment plans, followed by the maintenance dose; clinicians may omit the loading regimen when a slower start is preferable.
- Swallow the tablet with water.
- Take it at approximately the same time each day.
- It may be taken with or without food.
- Swallow it whole rather than crushing or chewing it.
- If a dose is missed, take it when remembered unless the next dose is near.
- Do not take two doses together to compensate for a missed tablet.
- Continue monitoring appointments even when joint symptoms improve.
A reduced maintenance dose may be considered when the prescribed dose causes tolerability problems, but this decision belongs to the prescriber. The FDA prescribing information specifies liver monitoring and blood-pressure checks during treatment [2].
How it works
Leflunomide is converted in the body to its active metabolite, teriflunomide. This metabolite inhibits dihydro-orotate dehydrogenase, an enzyme needed for de novo pyrimidine synthesis.
Pyrimidines are building blocks required for DNA and RNA production. Activated lymphocytes need rapid nucleotide production when they multiply during an autoimmune response. By reducing pyrimidine availability, leflunomide limits the expansion of certain activated T and B lymphocytes.
The result is immunomodulation rather than complete immune-system suppression. In practical terms, the medicine reduces part of the immune activity that maintains synovial inflammation. The European Medicines Agency describes Arava as a treatment for active rheumatoid arthritis and active psoriatic arthritis in adults [1].
The long half-life of the active metabolite explains why leflunomide can remain in the body for an extended period after treatment stops. A drug-elimination procedure may be required when rapid removal is medically necessary, such as severe toxicity or pregnancy planning.
Indications
Rheumatoid arthritis is an autoimmune inflammatory disease in which the immune system attacks the lining of joints. Persistent inflammation can cause pain, swelling, morning stiffness, reduced movement, and progressive joint damage.
Psoriatic arthritis is an inflammatory arthritis associated with psoriasis. It may affect the fingers, toes, spine, tendon attachments, or several joint groups at the same time.
Arava may be prescribed when active inflammatory arthritis requires a conventional DMARD. The aim is to reduce disease activity, limit swelling and tenderness, preserve physical function, and slow damage visible on clinical examination or imaging.
Treatment response varies. Some people notice improved stiffness and swelling within the first several weeks, while disease control may take longer. Early symptom change does not always indicate sustained disease control. Follow-up assessment helps distinguish temporary relief from lasting improvement. A rheumatologist may combine leflunomide with another antirheumatic strategy when one medicine does not control inflammation adequately.
Comparison
Arava belongs to the conventional synthetic DMARD category. This class is used to modify inflammatory arthritis over months and years, while symptomatic medicines mainly reduce pain or stiffness without controlling the underlying immune process.
| Treatment category | Main role | Main limitation |
|---|---|---|
| Leflunomide DMARD | Reduces immune-driven inflammation and may slow joint damage | Requires liver, blood-count, infection, and pregnancy precautions |
| Methotrexate DMARD | Common foundation treatment for several inflammatory arthritides | Can cause liver, blood-count, lung, or gastrointestinal problems |
| Targeted biologic or synthetic DMARD | Acts on a defined immune pathway when conventional therapy is insufficient | Greater monitoring burden and infection-related precautions |
Leflunomide may suit adults who need a conventional DMARD and cannot use, tolerate, or adequately respond to another option. Methotrexate may be selected more often in some treatment pathways, while biologic or targeted medicines may be considered after inadequate response to conventional DMARD therapy.
The comparison is clinical, not a ranking. The right choice depends on diagnosis, disease severity, liver and kidney health, pregnancy plans, infection history, blood-test results, and previous treatment response.
Contraindications
The medicine should not be used in the following situations:
- Pregnancy
- Breastfeeding
- Severe liver disease
- Serious impairment of liver function
- Severe immune deficiency
- Serious bone-marrow disorders
- Markedly low white-cell, red-cell, or platelet counts
- Severe uncontrolled infection
- Known hypersensitivity to leflunomide or teriflunomide
- Use with teriflunomide
Important interaction groups include:
- Methotrexate and other hepatotoxic medicines
- Teriflunomide
- Certain immunosuppressive treatments
- Warfarin and other medicines requiring close coagulation monitoring
- Some medicines that affect blood-cell counts
- Live vaccines
The WHO describes immunosuppressive and immunomodulatory treatment as a factor that can alter infection risk and vaccination decisions [3].
When this is not for you
Arava is not for you if you are pregnant or breastfeeding, have serious liver problems, a severe infection, or a serious condition affecting your immune system or bone marrow. It may also be unsuitable if you have very low blood-cell counts, are allergic to leflunomide or teriflunomide, or already take teriflunomide.
Tell your doctor before treatment if you have had tuberculosis exposure, hepatitis, recurrent infections, or significant lung disease. Women who could become pregnant need reliable contraception, and anyone planning pregnancy should speak with a clinician before taking the medicine. Alcohol should be limited or avoided because it can add stress to the liver.
Side effects
Common adverse effects include diarrhoea, nausea, indigestion, headache, hair thinning, skin rash, and mild increases in blood pressure. Some patients find gastrointestinal effects most noticeable during the first weeks.
Liver injury is a major safety concern. The risk can increase with alcohol use or other medicines that affect the liver. Blood tests commonly include alanine aminotransferase and other liver-function measurements.
Contact the prescribing service promptly for:
- Yellowing of the skin or eyes
- Dark urine or unusually pale stools
- Severe or persistent abdominal pain
- Marked weakness or unexplained bruising
- Fever, recurrent infections, or painful mouth ulcers
- New cough or breathing difficulty
- A widespread blistering or peeling rash
- Significant blood-pressure elevation
Hair thinning can be distressing but may improve after treatment adjustment or discontinuation. Diarrhoea should not be ignored if it is persistent, causes dehydration, or occurs with fever.
Common mistakes
Several avoidable errors can reduce treatment quality or increase risk:
- Expecting immediate pain relief and stopping after a few doses
- Taking two tablets after forgetting one dose
- Missing liver-function or blood-count monitoring
- Assuming mild diarrhoea cannot be treatment-related
- Drinking heavily while taking leflunomide
- Starting another immune-modifying medicine without coordination
- Failing to report a new infection before the next dose
- Continuing treatment after a positive pregnancy test
- Forgetting to mention Arava before receiving a vaccine
- Treating hair loss or a rash as unrelated without reporting it
- Crushing the tablet because it appears difficult to swallow
- Assuming a prior normal liver test removes the need for future testing
What doctors say
In clinical practice, rheumatologists usually judge Arava by disease activity rather than by pain relief during the first few days. A reduction in swollen joints and morning stiffness is more meaningful than a single comfortable day.
Doctors also pay attention to laboratory trends. A mildly abnormal liver result may require repeat testing, while a substantial or persistent rise can require treatment interruption and drug elimination. Regular blood pressure checks are useful because hypertension may develop during therapy.
Another practical point concerns the medicine’s persistence. A patient who stops Arava because of a serious adverse effect may still have active metabolite in the body. The elimination procedure uses medicines such as cholestyramine or activated charcoal under medical supervision.
Rheumatology guidelines from the American College of Rheumatology place conventional DMARDs within structured, treat-to-target care, where therapy is adjusted according to disease activity and response [4].
Frequently asked questions
Is Arava a steroid?
No. Arava contains leflunomide, a conventional synthetic DMARD rather than a corticosteroid. It changes selected immune-cell activity and is used for long-term inflammatory arthritis control. The EMA identifies leflunomide as the active substance responsible for Arava’s therapeutic action. The EMA product information available in 2025 supports this classification.
How long does Arava take to work?
Improvement often develops over several weeks, while fuller disease control may take longer. The timing depends on arthritis severity, previous treatment, adherence, and whether another DMARD is being used. FDA-reviewed prescribing information describes Arava as a continuing treatment rather than an as-needed medicine. The FDA prescribing information available in 2024 supports this dosing approach.
Can Arava be taken with food?
Yes. Arava can generally be taken with or without food, provided it is taken consistently once daily. Taking it after food may make nausea easier for some people, although persistent gastrointestinal symptoms require medical review. The European Medicines Agency product information supports oral administration without a food-specific restriction. The EMA product information available in 2025 confirms this administration guidance.
Can Arava be used during pregnancy?
No. Leflunomide may cause serious fetal harm and requires pregnancy precautions during treatment. Anyone who becomes pregnant while taking Arava needs prompt medical assessment, and a drug-elimination procedure may be required. WHO immunisation and medication-safety principles support individual planning when immune-modifying therapy is used during reproductive years. WHO guidance available in 2023 supports this individualized safety planning.
Does Arava require regular blood tests?
Yes. Monitoring generally includes liver enzymes, complete blood counts, and blood pressure, especially during the early months or after a treatment change. The frequency depends on clinical circumstances and local rheumatology practice. NICE guidance for rheumatoid arthritis supports regular safety monitoring for conventional DMARD treatment [5]. NICE guidance published in 2020 provides this monitoring framework.
What happens if Arava causes a serious reaction?
The medicine may need to be stopped, and the active metabolite may need to be removed rapidly with a prescribed elimination procedure. Warning signs include jaundice, severe rash, breathing difficulty, serious infection, major blood-count changes, or marked liver-test abnormalities. The FDA label describes cholestyramine or activated charcoal as options used for accelerated elimination under medical supervision. The FDA prescribing information available in 2024 supports these elimination options.
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Comparison
Compare all medications for Rheumatoid ArthritisArava: Reviews and Experiences
I expected the tablets to work like a painkiller and became discouraged early on. My swollen fingers improved later, but I needed regular blood tests and had to be more careful with alcohol.
Joint tenderness improved enough for me to walk more comfortably. Hair shedding became noticeable, so my rheumatologist reviewed the treatment and monitored my blood results.
The medicine reduced morning stiffness, but diarrhoea remained troublesome. The treatment was changed after discussion rather than simply stopping it at home.
Sources
- European Medicines Agency (2025). Arava — Product information.
- U.S. Food and Drug Administration (2024). ARAVA (leflunomide) tablets, prescribing information.
- World Health Organization (2023). WHO consolidated guidelines on tuberculosis: Module 3 — Diagnosis, rapid diagnostics for tuberculosis detection.
- American College of Rheumatology (2021). 2021 American College of Rheumatology Guideline for the Treatment of Rheumatoid Arthritis.
- National Institute for Health and Care Excellence (2020). Rheumatoid arthritis in adults: management — NICE guideline NG100.