Lupus (SLE) Medications: Treatment Guide & Drug Options
📊 Quick Facts About SLE Medications
💡 Key Takeaways About Lupus Treatment
- Hydroxychloroquine is essential: Almost all SLE patients should take this medication unless contraindicated - it reduces flares, protects organs, and is safe during pregnancy
- Multiple drugs often needed: Most patients require a combination of medications to control their disease effectively
- Treatment is tailored: Your medication regimen depends on which organs are affected and how severe your symptoms are
- Corticosteroids work fast but have risks: While effective for flares, long-term high-dose steroids have significant side effects
- Biologics for difficult cases: Newer biologic drugs like belimumab and anifrolumab help when standard treatments aren't enough
- Pregnancy requires planning: Some medications must be stopped months before conception, while others are safe to continue
- Regular monitoring is crucial: Blood tests and eye exams help detect and prevent medication side effects
What Medications Are Used to Treat Lupus (SLE)?
The main medications for lupus include antimalarials (hydroxychloroquine), corticosteroids (prednisone), immunosuppressants (azathioprine, mycophenolate, methotrexate, cyclophosphamide), and biologics (belimumab, rituximab, anifrolumab). Most patients need multiple medications, with hydroxychloroquine recommended for nearly everyone with SLE.
Systemic lupus erythematosus (SLE) is a complex autoimmune disease where the immune system attacks healthy tissues throughout the body. Because the disease can affect many different organs and varies greatly between individuals, treatment must be personalized. The medications used for lupus fall into several categories, each targeting different aspects of the disease process.
The fundamental principle of lupus treatment is that symptoms should be treated when they occur, and medication can often be reduced or stopped during periods of remission. However, certain medications - particularly hydroxychloroquine - are recommended as long-term maintenance therapy for most patients because they provide ongoing protection against flares and organ damage.
Your rheumatologist will develop a treatment plan based on several factors: which organs are affected, how severe your symptoms are, your overall health status, and whether you're planning pregnancy. Treatment goals include controlling active disease, preventing flares, minimizing organ damage, and maintaining quality of life while minimizing medication side effects.
Overview of Lupus Medication Classes
Understanding the different types of medications helps you participate in treatment decisions. Here's an overview of the main drug classes used in lupus treatment:
- Antimalarial drugs (hydroxychloroquine): The cornerstone of lupus treatment, recommended for nearly all patients
- Nonsteroidal anti-inflammatory drugs (NSAIDs): For mild joint and muscle pain
- Corticosteroids: Powerful anti-inflammatory drugs for moderate to severe symptoms
- Immunosuppressants: Drugs that reduce immune system activity, used for serious organ involvement
- Biologic drugs: Targeted therapies that block specific immune system pathways
| Drug Class | Examples | Primary Uses | Onset of Action |
|---|---|---|---|
| Antimalarials | Hydroxychloroquine, Chloroquine | Maintenance therapy, skin/joint symptoms | 1-3 months |
| Corticosteroids | Prednisone, Methylprednisolone | Active flares, rapid symptom control | Days to weeks |
| Immunosuppressants | Azathioprine, Mycophenolate, Cyclophosphamide | Severe organ involvement, steroid-sparing | Weeks to months |
| Biologics | Belimumab, Rituximab, Anifrolumab | Refractory disease, add-on therapy | Weeks to months |
How Do Antimalarial Drugs Help Treat Lupus?
Antimalarial drugs, particularly hydroxychloroquine (Plaquenil), are the foundation of lupus treatment. They reduce disease flares by 50%, protect against organ damage, decrease cardiovascular risk, and are one of the few lupus medications safe during pregnancy. All SLE patients should take hydroxychloroquine unless they have a specific contraindication.
Although originally developed to prevent and treat malaria, antimalarial medications have become essential in lupus treatment. Hydroxychloroquine is the most commonly used, with chloroquine as an alternative. These drugs work by modulating the immune system's inflammatory response, though their exact mechanism in lupus isn't completely understood. What we do know is that they interfere with how immune cells communicate and respond to triggers that would otherwise cause inflammation.
The benefits of hydroxychloroquine extend far beyond controlling symptoms. Research has consistently shown that patients who take hydroxychloroquine have fewer disease flares, better long-term survival, reduced risk of blood clots, lower cholesterol levels, and decreased risk of developing kidney disease. These protective effects make it one of the most valuable medications in lupus treatment, which is why international guidelines recommend it for all SLE patients without contraindications.
One of the most important aspects of hydroxychloroquine is its safety during pregnancy. Unlike many other lupus medications, hydroxychloroquine should be continued throughout pregnancy because stopping it increases the risk of disease flares. Studies have shown that pregnant women who continue hydroxychloroquine have better outcomes for both themselves and their babies.
Taking Hydroxychloroquine
Hydroxychloroquine is taken as a tablet, typically once or twice daily. The standard dose is 200-400mg daily, usually calculated based on body weight to minimize side effects. It takes 1-3 months for the medication to reach full effectiveness, so patience is important when starting treatment. Because the benefits are long-term and cumulative, consistent daily use is essential.
Precautions and Monitoring
You should not take hydroxychloroquine without consulting your doctor if you have:
- Epilepsy or seizure disorders
- Porphyria (a blood disorder)
- Pre-existing retinal or vision problems
- Significant hearing impairment
Smoking reduces the effectiveness of hydroxychloroquine, providing another reason to quit if you haven't already. Regular eye examinations are required during long-term treatment because, rarely, hydroxychloroquine can affect the retina. Current guidelines recommend a baseline eye exam, then annual screening starting after 5 years of use (or earlier if you have additional risk factors). The risk of retinal toxicity is very low with modern dosing guidelines, and early detection through screening allows the medication to be stopped before any permanent damage occurs.
Side Effects of Antimalarials
Most people tolerate hydroxychloroquine well. When side effects occur, they're usually mild and often improve with time:
- Gastrointestinal symptoms: Nausea, loss of appetite, stomach discomfort - often reduced by taking with food
- Skin changes: Rashes, itching, or changes in skin pigmentation
- Visual changes: Difficulty focusing between near and far vision - usually temporary and reversible
While retinal toxicity is a serious potential side effect, it's rare with proper dosing and monitoring. The risk increases with higher doses and longer treatment duration. Regular ophthalmologic screening allows early detection before any symptoms or permanent damage occur. Don't skip your eye appointments, but also don't let fear of this rare side effect prevent you from taking this beneficial medication.
When Are Corticosteroids Used for Lupus?
Corticosteroids like prednisone are powerful anti-inflammatory drugs used during lupus flares and for severe organ involvement. They work quickly and can be life-saving in serious situations. However, long-term high-dose use causes significant side effects including osteoporosis, weight gain, diabetes, and increased infection risk, so doctors try to use the lowest effective dose.
Corticosteroids (often simply called "steroids" - not to be confused with anabolic steroids) are among the most effective medications for controlling lupus inflammation. They work by suppressing immune system activity and reducing the inflammatory response that damages tissues. Prednisone is the most commonly prescribed oral corticosteroid, though methylprednisolone may be given intravenously for severe flares.
The power of corticosteroids makes them invaluable for rapidly controlling serious symptoms. In some situations, such as severe lupus nephritis (kidney inflammation) or lupus affecting the brain, high-dose corticosteroids can be life-saving. They typically provide relief within days, much faster than other lupus medications.
However, this effectiveness comes with a significant downside: long-term use of moderate to high doses causes numerous side effects. This creates a treatment challenge - corticosteroids may be necessary to control the disease, but prolonged use can cause problems that may be as serious as the lupus itself. The solution is to use corticosteroids strategically: higher doses during flares, then tapering to the lowest effective dose or stopping completely when possible.
Forms of Corticosteroids
Corticosteroids come in several forms for lupus treatment:
- Oral tablets (prednisone): Most common form for ongoing treatment
- Intravenous infusion (methylprednisolone): High-dose "pulse" therapy for severe flares
- Topical creams/ointments: For skin manifestations of lupus
- Joint injections: For isolated joint inflammation
The Steroid Taper
When you've been taking corticosteroids for more than a few weeks, you cannot simply stop taking them. Your body naturally produces cortisol (the hormone that corticosteroids mimic), but when you take corticosteroids, your adrenal glands reduce their own production. Stopping suddenly can cause adrenal insufficiency, a potentially dangerous condition.
Instead, your doctor will gradually reduce your dose - this is called "tapering." The speed of tapering depends on how long you've been taking steroids, your current dose, and whether your lupus symptoms are well-controlled. Some patients can eventually stop completely, while others need a low maintenance dose.
Side Effects of Corticosteroids
Side effects depend on dose and duration of use. Short-term, low-dose treatment may cause minimal problems, while long-term high-dose therapy can lead to:
- Metabolic effects: Weight gain, increased blood sugar (potentially diabetes), elevated cholesterol
- Bone effects: Osteoporosis, increased fracture risk
- Immune effects: Increased susceptibility to infections
- Skin changes: Thin, fragile skin; easy bruising; poor wound healing
- Eye problems: Cataracts, glaucoma
- Mood changes: Anxiety, irritability, difficulty sleeping
- Appearance changes: "Moon face," fat redistribution, acne
If you've been taking corticosteroids for more than a few weeks, stopping suddenly can cause serious health problems. Always work with your doctor to taper gradually. If you're having side effects, talk to your rheumatologist about adjusting your treatment - don't stop on your own.
What Are Immunosuppressant Drugs for Lupus?
Immunosuppressants are medications that reduce immune system activity to control severe lupus. Common options include azathioprine (Imuran), mycophenolate mofetil (CellCept), methotrexate, and cyclophosphamide. They're used for serious organ involvement, particularly lupus nephritis, and as "steroid-sparing" agents to allow lower corticosteroid doses.
Immunosuppressant medications work by inhibiting the ability of immune cells to multiply and function. Because the overactive immune response is what causes lupus symptoms and organ damage, reducing immune system activity can control the disease. These medications are sometimes called "cytotoxic" or "cell-inhibiting" drugs because they affect rapidly dividing cells.
Immunosuppressants are typically reserved for moderate to severe lupus, particularly when major organs like the kidneys are involved. They're also valuable as "steroid-sparing" agents - by controlling the disease, they allow patients to reduce or stop corticosteroids and avoid steroid-related side effects. The trade-off is that immunosuppressants have their own side effects, particularly increased infection risk, and require regular blood monitoring.
These medications take several weeks to months to reach full effectiveness. During this time, corticosteroids often provide disease control while the immunosuppressant builds up in your system. Once the immunosuppressant is working, your doctor will typically taper the steroid dose.
Types of Immunosuppressants
Azathioprine (Imuran) is often the first-choice immunosuppressant for many lupus patients. It's particularly useful for maintaining remission after a flare has been controlled and for patients planning pregnancy (it's considered relatively safe during pregnancy with proper monitoring). Azathioprine requires a genetic test before starting because some people lack an enzyme needed to process the drug safely.
Mycophenolate mofetil (CellCept) is commonly used for lupus nephritis (kidney involvement) and has become a preferred option for both inducing remission and maintenance therapy. It's generally well-tolerated, though gastrointestinal side effects are common initially. Mycophenolate cannot be used during pregnancy and must be stopped at least 6 weeks before conception.
Methotrexate is particularly helpful when joint symptoms are prominent. It's been used for decades in rheumatoid arthritis and is effective for lupus-related joint pain and skin problems. Methotrexate is taken weekly (not daily) and requires folic acid supplementation to reduce side effects. It must be stopped at least 3 months before pregnancy.
Cyclophosphamide is reserved for severe, life-threatening lupus - particularly severe kidney involvement or central nervous system disease. It's one of the most powerful immunosuppressants but also has the most significant side effects, including risk of infertility. Treatment is usually given as intermittent intravenous infusions rather than daily pills.
Precautions When Taking Immunosuppressants
Important considerations for immunosuppressant therapy:
- Drug interactions: Always tell your doctor about all medications you take, particularly with azathioprine
- Grapefruit: Avoid grapefruit and grapefruit juice with cyclophosphamide
- Alcohol: Limit or avoid alcohol as it increases nausea and liver stress
- Dehydration: Contact your doctor if you're ill with vomiting or diarrhea, as dehydration can affect how your kidneys process these medications
- Sun protection: Use sunscreen consistently, as immunosuppression increases skin cancer risk
Handling Immunosuppressant Medications
Some immunosuppressants require careful handling to prevent others from being exposed:
- Don't crush or split tablets unless specifically instructed
- Wash hands after handling medications
- Return unused medications to a pharmacy - don't discard in regular trash
Pregnancy Considerations
Most immunosuppressants are not safe during pregnancy. If you're planning to become pregnant:
- Discuss with your rheumatologist well in advance
- Use reliable contraception during treatment
- Stop the medication 3-6 months before trying to conceive (exact timing depends on the drug)
- This applies to both women and their male partners for some medications
Azathioprine is an exception - it can often be continued during pregnancy with proper monitoring. Your doctor will help you plan a safe approach.
Infection Risk
Because immunosuppressants reduce immune function, you're more susceptible to infections. Seek medical attention promptly if you develop:
- Fever or chills
- Persistent cough or sore throat
- Diarrhea
- Skin rashes
- Frequent urination or burning with urination
- Any signs of infection
Side Effects and Monitoring
Common side effects include nausea and gastrointestinal upset, particularly when starting treatment. These often improve with time. More serious concerns include:
- Bone marrow suppression: Reduced blood cell production, causing anemia, low white blood cells, or low platelets
- Liver effects: Some immunosuppressants can affect liver function
- Kidney effects: Particularly with cyclosporine
Regular blood tests are essential during immunosuppressant therapy to monitor for these effects and catch any problems early. Your doctor will schedule these based on which medication you're taking and how long you've been on it.
What Are Biologic Drugs for Lupus?
Biologic drugs are targeted therapies that block specific immune system pathways involved in lupus. Currently approved biologics include belimumab (Benlysta), rituximab (Rituxan - used off-label), and anifrolumab (Saphnelo). They're used when standard treatments aren't sufficient, particularly for skin, joint, and kidney symptoms that don't respond to conventional therapy.
Biologic medications represent a newer approach to treating lupus. Unlike traditional immunosuppressants that broadly suppress the immune system, biologics target specific molecules or cells involved in the disease process. This targeted approach can be more effective for some patients and may have different side effect profiles than conventional drugs.
Biologics are typically added to existing therapy when hydroxychloroquine and immunosuppressants haven't adequately controlled the disease. They're particularly helpful for patients with active disease despite standard treatment, those who cannot tolerate conventional medications, or those who need ongoing corticosteroids and would benefit from a steroid-sparing medication.
The time to see benefit varies between biologics. Some, like rituximab, can show effects relatively quickly in responsive patients, while others may take up to six months for full effect. If a biologic is working well, treatment typically continues long-term.
Available Biologic Medications
Rituximab is the most commonly used biologic for severe lupus, particularly lupus nephritis. It works by depleting B cells, a type of immune cell that produces the autoantibodies causing inflammation in lupus. Although not officially FDA-approved for lupus, it's widely used "off-label" based on clinical evidence and is included in treatment guidelines.
Belimumab (Benlysta) was the first biologic specifically approved for lupus. It blocks a protein called BLyS (B-lymphocyte stimulator) that helps B cells survive. Belimumab is particularly effective for skin and joint symptoms and has been shown to reduce flares and allow steroid reduction. It's available as both an intravenous infusion and a self-administered subcutaneous injection.
Anifrolumab (Saphnelo) is a newer biologic that blocks type I interferon signaling, a pathway that's overactive in many lupus patients. It's particularly helpful for skin involvement and overall disease activity that hasn't responded to standard treatment.
Taking Biologic Medications
Biologics are given either as:
- Intravenous infusions: Given in a medical setting, typically every few weeks to months
- Subcutaneous injections: Self-administered at home after training (available for belimumab)
Precautions with Biologics
Because biologics affect the immune system:
- Pause treatment if you develop an infection
- Wait until the infection clears before resuming
- Treatment may need to be paused before surgery
- Avoid biologics during pregnancy - discuss with your doctor well before planning pregnancy
Side Effects of Biologics
Common side effects include:
- Increased infection risk: Similar to other immunosuppressants
- Infusion reactions: Chills, fever, muscle aches during or after IV infusions - usually manageable with premedication
- Injection site reactions: Redness or swelling where subcutaneous injections are given - typically mild
These side effects, particularly the flu-like symptoms, often occur early in treatment and typically improve with subsequent doses.
What Other Medications Might Be Needed with Lupus?
Lupus patients often need additional medications for complications and associated conditions. Common additions include blood thinners for blood clots, blood pressure medications, cholesterol-lowering drugs, and osteoporosis treatments. NSAIDs may be used for mild pain, and medications for depression and anxiety are sometimes needed.
Lupus can affect multiple organ systems and increase the risk of various complications. Additionally, some lupus medications (particularly corticosteroids) can cause conditions that require their own treatment. This means many lupus patients take medications beyond those directly targeting the autoimmune disease.
NSAIDs for Pain Management
Nonsteroidal anti-inflammatory drugs (NSAIDs) like ibuprofen and naproxen can help with mild joint and muscle pain. They reduce inflammation and provide pain relief relatively quickly. However, NSAIDs:
- Don't prevent long-term damage or affect disease progression
- Are usually combined with other treatments
- Should be used cautiously if you have kidney problems, heart disease, or stomach ulcers
- Can interact with blood thinners
Blood Thinners
Many lupus patients have an increased risk of blood clots, particularly those with antiphospholipid antibodies. If you've had a blood clot, you'll likely need anticoagulation therapy:
- Acute treatment: Injectable heparin (low-molecular-weight heparin)
- Long-term prevention: Warfarin (Coumadin) tablets, requiring regular blood monitoring
Always inform emergency medical providers that you have lupus if you experience a blood clot, as this affects treatment decisions.
Treatments for Other Complications
Depending on how lupus affects you, additional medications might include:
- Blood pressure medications: If you develop hypertension, particularly with kidney involvement
- Cholesterol-lowering drugs (statins): To reduce cardiovascular risk
- Osteoporosis medications: To prevent or treat bone loss, especially if you take corticosteroids
- Antidepressants or anti-anxiety medications: Living with a chronic illness can affect mental health
A Note on Estrogen
Estrogen can trigger lupus flares in some patients. Discuss with your doctor before taking:
- Birth control pills containing estrogen
- Hormone replacement therapy for menopause symptoms
There are often estrogen-free alternatives available if you need contraception or symptom relief.
How Is Lupus Treatment Approached?
Lupus treatment follows a "treat-to-target" approach: controlling active disease, achieving remission or low disease activity, preventing flares, and minimizing medication side effects. Treatment intensity matches disease severity - mild symptoms may need only hydroxychloroquine and occasional NSAIDs, while severe organ involvement requires aggressive immunosuppression.
Modern lupus treatment follows a strategic approach that balances disease control with medication risks. The treatment goals, endorsed by international organizations like EULAR (European Alliance of Associations for Rheumatology) and ACR (American College of Rheumatology), focus on achieving the best possible disease control with the fewest medications at the lowest effective doses.
Treatment During Flares
When lupus flares - periods of increased disease activity - treatment is intensified to regain control. Mild to moderate flares might be managed with increased antimalarial doses, short courses of NSAIDs, or low-dose corticosteroids. Severe flares, particularly those affecting major organs, may require high-dose corticosteroids (sometimes given intravenously) along with immunosuppressants.
Severe Flares Requiring Hospitalization
Some severe flares require hospital admission, particularly when:
- The kidneys are severely affected (lupus nephritis)
- The central nervous system is involved
- Severe blood abnormalities develop (severe anemia, very low platelets)
Hospital treatment typically starts with high-dose intravenous corticosteroids, then transitions to oral medications as the situation stabilizes. Immunosuppressants are often started during hospitalization and continued long-term.
Maintenance Therapy
Once a flare is controlled, treatment shifts to maintenance - keeping the disease quiet while minimizing medication side effects. Most patients remain on hydroxychloroquine indefinitely. Corticosteroid doses are tapered as low as possible, ideally to zero. Immunosuppressants may be continued as maintenance therapy for patients with a history of severe disease or organ involvement.
Children with Lupus
Children can develop lupus, and they receive the same types of medications as adults, with doses adjusted for their weight. Pediatric rheumatologists specialize in treating children with lupus and work closely with families to manage the disease while minimizing impacts on growth and development.
Lupus requires ongoing monitoring even when you feel well. Regular appointments allow your rheumatologist to catch early signs of flares, monitor for medication side effects, adjust treatment as needed, and address any concerns. Blood tests and urine tests are typically done regularly to monitor disease activity and organ function.
Frequently Asked Questions About Lupus Medications
Hydroxychloroquine (Plaquenil) is considered the cornerstone medication for nearly all SLE patients. It reduces disease flares by approximately 50%, protects organs from damage, decreases cardiovascular risk, and is one of the few lupus medications safe during pregnancy. The 2023 EULAR guidelines recommend hydroxychloroquine for all lupus patients without specific contraindications.
However, "best" depends on your individual situation. Most patients need additional medications such as corticosteroids for flares, immunosuppressants for organ involvement, or biologics for difficult-to-control disease. Your rheumatologist will create a personalized treatment plan based on which organs are affected and how severe your symptoms are.
Currently, there is no cure for lupus (SLE). However, medications can effectively control the disease and put it into remission - a state where you have minimal or no symptoms. Many people achieve remission with proper treatment and can live normal, active lives.
The goal of treatment is to prevent flares, reduce organ damage, and maintain quality of life. With advances in understanding lupus biology and new medications being developed, treatment options continue to improve. Some patients achieve long-term remission and may be able to reduce their medications, though most need ongoing therapy.
Side effects vary by medication class:
Hydroxychloroquine: Generally well-tolerated. Rare risk of retinal toxicity with long-term use (requires regular eye exams). May cause nausea or skin changes.
Corticosteroids: Weight gain, osteoporosis, elevated blood sugar (potentially diabetes), increased infection risk, mood changes, easy bruising, cataracts. Risk increases with dose and duration.
Immunosuppressants: Increased infection risk, bone marrow suppression (low blood counts), liver effects, gastrointestinal upset. Require regular blood monitoring.
Biologics: Increased infection risk, infusion or injection site reactions, flu-like symptoms early in treatment.
Some lupus medications are safe during pregnancy while others must be stopped well in advance:
Safe during pregnancy: Hydroxychloroquine (should be continued - stopping increases flare risk), low-dose prednisone, azathioprine (with monitoring)
Must be stopped before pregnancy: Mycophenolate (at least 6 weeks before), methotrexate (at least 3 months before), cyclophosphamide (at least 3 months before), biologics (timing varies - discuss with your doctor)
Always discuss pregnancy plans with your rheumatologist well in advance. Pregnancy in lupus requires careful planning and monitoring. The good news is that with proper preparation and care, most women with lupus can have successful pregnancies.
Lupus is a chronic condition, and most patients need long-term treatment:
Hydroxychloroquine: Typically taken indefinitely due to its protective benefits
Corticosteroids: Used for flares, then tapered to the lowest effective dose or stopped if possible
Immunosuppressants: Duration varies - some patients can reduce or stop after sustained remission, while others need ongoing maintenance therapy
Biologics: Usually continued long-term if effective
Treatment is individualized based on your disease activity. Your rheumatologist will regularly assess whether medications can be reduced. Never stop medications without discussing with your doctor, as this risks triggering a flare.
Medical References & Sources
This article is based on current international guidelines and peer-reviewed medical literature:
- Fanouriakis A, et al. EULAR recommendations for the management of systemic lupus erythematosus: 2023 update. Ann Rheum Dis. 2024;83(1):15-29. doi:10.1136/ard-2023-224762
- Hahn BH, et al. American College of Rheumatology guidelines for screening, treatment, and management of lupus nephritis. Arthritis Care Res. 2012;64(6):797-808.
- Ruiz-Irastorza G, et al. Clinical efficacy and side effects of antimalarials in systemic lupus erythematosus: a systematic review. Ann Rheum Dis. 2010;69(1):20-28.
- Furie R, et al. Anifrolumab, an Anti-Interferon-alpha Receptor Monoclonal Antibody, in Moderate-to-Severe Systemic Lupus Erythematosus. Arthritis Rheumatol. 2017;69(2):376-386.
- Navarra SV, et al. Efficacy and safety of belimumab in patients with active systemic lupus erythematosus. Lancet. 2011;377(9767):721-731.
- World Health Organization. WHO Model List of Essential Medicines. 23rd List, 2023.
- Petri M, et al. Derivation and validation of the Systemic Lupus International Collaborating Clinics classification criteria for systemic lupus erythematosus. Arthritis Rheum. 2012;64(8):2677-2686.
About Our Medical Editorial Team
This article was written and reviewed by the iMedic Medical Editorial Team, which includes board-certified specialists in rheumatology, immunology, and internal medicine. Our content follows the GRADE evidence framework and adheres to guidelines from the American College of Rheumatology (ACR), European Alliance of Associations for Rheumatology (EULAR), and World Health Organization (WHO).
All medical information is reviewed for accuracy by licensed physicians and updated regularly to reflect current evidence and guidelines. Our editorial process ensures independence from pharmaceutical industry influence.
Last medical review: December 15, 2025
Next scheduled review: June 2026