When evaluating treatment options, Hydroxychloroquine is a synthetic antimalarial also used for autoimmune diseases like lupus and rheumatoid arthritis. It surged into the spotlight during the COVID‑19 pandemic, prompting countless headlines and a flood of questions about how it stacks up against other drugs.
Key Takeaways
- Hydroxychloroquine is approved for malaria and certain autoimmune conditions, not for COVID‑19.
- Most alternatives (e.g., remdesivir, ivermectin) have different mechanisms and varying levels of clinical evidence.
- Safety profiles differ markedly: hydroxychloroquine can affect the heart, while remdesivir may impact liver function.
- Cost and accessibility range from inexpensive generic pills to pricey IV formulations.
- Choosing a drug depends on the specific disease, severity, and individual risk factors.
Hydroxychloroquine is often confused with its older cousin chloroquine, but the two are not interchangeable. Below we break down how hydroxychloroquine works, then compare it with the most talked‑about alternatives.
How Hydroxychloroquine Works
The drug interferes with the parasite’s ability to digest hemoglobin, which is why it treats malaria. In autoimmune disorders, it modulates the immune system by dampening cytokine production and reducing the activity of toll‑like receptors. Dosage for malaria typically starts at 800mg on day1, followed by 400mg daily for two days. For rheumatoid arthritis, the usual dose is 200-400mg daily, taken with food to lessen stomach upset.
Common Alternatives and Their Core Traits
When doctors look for substitutes, they consider the disease target, evidence base, and side‑effect profile. The following drugs are the most frequently mentioned alternatives to hydroxychloroquine in recent medical discussions.
Chloroquine is a first‑generation antimalarial that shares a similar chemical backbone with hydroxychloroquine. It was once used for lupus but fell out of favor due to higher toxicity, especially retinal damage.
Ivermectin is a broad‑spectrum antiparasitic approved for river blindness and certain worm infections. Early lab studies hinted at antiviral activity, sparking off‑label use for COVID‑19, though large trials have not confirmed a benefit.
Remdesivir is an RNA‑dependent RNA polymerase inhibitor originally developed for Ebola. It received Emergency Use Authorization for hospitalized COVID‑19 patients after showing modest reductions in recovery time.
Favipiravir is a viral RNA polymerase inhibitor used in Japan for influenza. Some trials in COVID‑19 have reported faster viral clearance, but data remain mixed.
Dexamethasone is a potent glucocorticoid that suppresses inflammation. It is not an antiviral but has saved lives in severe COVID‑19 by curbing the cytokine storm.
Tocilizumab is an IL‑6 receptor antagonist used for rheumatoid arthritis and cytokine release syndrome. It’s sometimes added to severe COVID‑19 protocols when inflammation spikes.
Azithromycin is a macrolide antibiotic with anti‑inflammatory properties. Early COVID‑19 regimens paired it with hydroxychloroquine, but subsequent studies showed no added benefit and highlighted cardiac risks.
Side‑Effect Snapshot
Understanding safety is crucial. Below is a quick guide to the most common adverse events each drug can cause.
- Hydroxychloroquine: QT‑interval prolongation, retinal toxicity (rare with short courses), gastrointestinal upset.
- Chloroquine: Higher risk of cardiac arrhythmia and retinal damage, especially at doses >1g/day.
- Ivermectin: Skin rash, dizziness, rare neurotoxicity at high doses.
- Remdesivir: Elevated liver enzymes, infusion‑related reactions, occasional kidney injury.
- Favipiravir: Elevated uric acid, teratogenic potential, mild liver enzyme rise.
- Dexamethasone: Hyperglycemia, mood swings, increased infection risk with prolonged use.
- Tocilizumab: Upper‑respiratory infections, liver enzyme elevation, neutropenia.
- Azithromycin: QT prolongation (especially with other QT‑prolonging drugs), diarrhea.

Cost and Accessibility Overview
Affordability can dictate real‑world use, especially in low‑resource settings.
- Hydroxychloroquine: Generic oral tablets cost £0.10-£0.30 per pill in the UK.
- Chloroquine: Similar price point to hydroxychloroquine, though availability has decreased.
- Ivermectin: Widely available as a cheap oral formulation; ~£0.20 per tablet.
- Remdesivir: Intravenous therapy costing several thousand pounds per treatment course; often limited to hospital formulary.
- Favipiravir: Not approved in the UK, but where available, price can exceed £100 per course.
- Dexamethasone: Inexpensive steroid, ~£0.05 per tablet.
- Tocilizumab: Expensive monoclonal antibody, £1,200-£1,800 per infusion.
- Azithromycin: Generic tablets cost around £0.15 each.
Comparison Table
Drug | Primary Mechanism | FDA/EMA Approval (as of 2025) | Typical Indication | COVID‑19 Evidence | Common Side Effects | Cost (UK, per typical course) |
---|---|---|---|---|---|---|
Hydroxychloroquine | Alkalinises lysosomes; immunomodulation | Approved for malaria, lupus, RA | Malaria prophylaxis; autoimmune disorders | Large RCTs show no benefit for COVID‑19 | QT prolongation, retinal toxicity (long‑term) | £15‑£30 (10‑day course) |
Chloroquine | Inhibits heme polymerisation in malaria parasite | Approved for malaria only (few countries) | Uncomplicated malaria | Similar to hydroxychloroquine - no proven benefit | QT prolongation, retinopathy | £12‑£25 (10‑day course) |
Ivermectin | Glutamate‑gated chloride channel agonist | Approved for parasitic infections | River blindness, strongyloidiasis | Observational data inconclusive; major trials negative | Dizziness, skin rash | £8‑£20 (5‑day course) |
Remdesivir | RNA‑polymerase inhibitor | Approved for hospitalized COVID‑19 (EU, US) | Severe COVID‑19 | Modest reduction in recovery time; not mortality benefit | Liver enzyme rise, infusion reactions | £3,000‑£5,000 (5‑day IV course) |
Favipiravir | Viral RNA‑polymerase inhibitor | Approved in Japan for influenza; off‑label elsewhere | Influenza (Japan); investigational COVID‑19 | Mixed results; some early trials positive | Hyperuricemia, teratogenic risk | £100‑£150 (10‑day course) |
Dexamethasone | Glucocorticoid receptor agonist | Approved for many inflammatory conditions | Severe inflammation, COVID‑19 (hospitalized) | Reduces mortality in ventilated patients | Hyperglycemia, mood changes | £5‑£10 (10‑day oral course) |
Tocilizumab | IL‑6 receptor blockade | Approved for rheumatoid arthritis, cytokine release syndrome | Severe COVID‑19 with high IL‑6 | Improves outcomes in selected high‑inflammation patients | Infection risk, liver enzyme rise | £1,500‑£1,800 (single infusion) |
Azithromycin | Protein synthesis inhibitor (macrolide) | Approved for bacterial infections | Respiratory bacterial infections | No proven antiviral benefit; combined trials negative | QT prolongation, GI upset | £12‑£20 (5‑day course) |
When to Choose Hydroxychloroquine Over Alternatives
If a patient already has a prescription for lupus or rheumatoid arthritis, hydroxychloroquine remains the drug of choice for disease control. Its oral form, low cost, and long safety record for chronic use make it hard to replace in these contexts. However, for acute viral infections or hospitalized COVID‑19 cases, the evidence points to other agents-remdesivir for early hospitalization, dexamethasone for patients needing oxygen, and tocilizumab for those with a cytokine surge.

Decision Checklist for Clinicians and Patients
- Identify the primary condition. Autoimmune disease → hydroxychloroquine; severe COVID‑19 → dexamethasone ± tocilizumab.
- Check regulatory status. Is the drug approved for the indication in your country?
- Assess cardiac risk. Review ECG for QT interval; avoid hydroxychloroquine or azithromycin if QT >450ms.
- Review liver and kidney function. Remdesivir and favipiravir need normal labs.
- Consider cost and administration route. Oral cheap drugs suit outpatient care; IV expensive drugs need hospital setting.
Frequently Asked Questions
Frequently Asked Questions
Is hydroxychloroquine effective for preventing COVID‑19?
Large randomized trials have consistently shown no protective benefit. Health agencies worldwide recommend against using it for COVID‑19 prophylaxis.
Can I take hydroxychloroquine and azithromycin together?
Both drugs can prolong the QT interval, increasing the risk of serious heart rhythm problems. Unless a doctor monitors your heart closely, the combination is generally discouraged.
What are the main side effects of remdesivir?
Patients may experience elevated liver enzymes, nausea, and occasional infusion‑related reactions. Kidney function should be checked before starting.
Is ivermectin safe for COVID‑19 treatment?
When used at approved doses for parasitic infections, ivermectin is safe. However, doses used in some COVID‑19 trials exceed approved levels and have caused neurotoxicity. Major health bodies advise against its use for COVID‑19.
When should dexamethasone be given to COVID‑19 patients?
Dexamethasone benefits patients who need supplemental oxygen or mechanical ventilation. Giving it too early, before oxygen is required, does not improve outcomes and may suppress viral clearance.
Bottom line: hydroxychloroquine remains a valuable drug for specific chronic conditions, but for acute viral illnesses-especially COVID‑19-other agents have clearer evidence or better safety. Always discuss with a healthcare professional before switching or combining medications.
All Comments
Ramanathan Valliyappa October 12, 2025
Hydroxychloroquine's cardiac risk is overstated by hype, but the data still show QT prolongation in susceptible patients.