Chloroquine is an antimalarial medicine used to prevent and treat malaria caused by chloroquine‑sensitive Plasmodium species and to treat extraintestinal amebiasis. It works by interfering with parasite heme detoxification inside red blood cells. While related to hydroxychloroquine, it is distinct and is not recommended for viral infections such as COVID‑19. Because dosing, safety monitoring, and drug interactions can be complex—especially with risks like QT prolongation and retinal toxicity—chloroquine in the United States is prescription‑only. Travelers and patients should seek individualized guidance from a clinician or travel medicine clinic to determine appropriate indications, dosing, and alternatives based on destination and history.
Chloroquine is primarily indicated for the prevention and treatment of malaria caused by chloroquine-sensitive Plasmodium species, most notably P. vivax, P. ovale, P. malariae, and some strains of P. falciparum where sensitivity persists. Because widespread resistance exists in many regions, particularly sub-Saharan Africa, Southeast Asia, and parts of South America, its use is geographically restricted based on up-to-date resistance maps from the CDC or WHO. It is also used to treat extraintestinal amebiasis caused by Entamoeba histolytica, typically in combination with a luminal agent to eradicate intestinal colonization.
Chloroquine is not the same as hydroxychloroquine. Hydroxychloroquine is often preferred for autoimmune conditions such as systemic lupus erythematosus and rheumatoid arthritis due to a more favorable safety profile. Chloroquine is generally not used for long-term autoimmune therapy in the U.S. and is not recommended for prevention or treatment of COVID-19; major guidelines advise against its use for viral infections outside of clinical trials.
Dosing of chloroquine varies by indication, patient weight, and the salt/base formulation. Many tablets contain chloroquine phosphate; 500 mg of chloroquine phosphate typically corresponds to approximately 300 mg of chloroquine base. Prescribers dose in mg/kg of base, so it is critical to follow a clinician’s instructions and the specific product label. Do not self-calculate or self-treat malaria; inappropriate dosing risks treatment failure, toxicity, and resistance.
Treatment of chloroquine-sensitive malaria in adults commonly follows a total dose of 25 mg base/kg over 3 days (for example, an initial dose followed by smaller doses at 6, 24, and 48 hours). For pediatric patients, weight-based dosing is essential, with maximum doses not exceeding adult totals. Because relapse prevention in P. vivax and P. ovale requires eradication of dormant liver forms, primaquine or tafenoquine may be prescribed after confirming G6PD status; do not attempt this without medical supervision.
Malaria prophylaxis with chloroquine (in areas with chloroquine-sensitive malaria only) is typically administered once weekly. Adults often receive the equivalent of 300 mg base weekly, starting 1–2 weeks before entering the endemic area, continuing weekly during exposure, and for 4 weeks after leaving. Children receive weight-based once-weekly doses (not exceeding the adult dose). Always verify destination-specific recommendations, as many travel regions require alternative agents due to resistance.
Administration tips: take chloroquine with food to reduce gastrointestinal upset. Avoid co-administration with antacids or kaolin-containing adsorbents, which can reduce absorption; if needed, separate by at least 4 hours. Adhere strictly to timing for malaria therapy to maintain effective blood levels and reduce the risk of treatment failure.
Cardiac safety is a key concern. Chloroquine can prolong the QT interval, potentially leading to serious arrhythmias, especially in patients with existing QT prolongation, structural heart disease, bradycardia, electrolyte abnormalities (low potassium or magnesium), or those taking other QT-prolonging drugs. A clinician may review your medication list and, when appropriate, obtain an ECG or labs before prescribing. Report palpitations, syncope, or new dizziness immediately.
Ophthalmologic effects are rare with short courses but more relevant with prolonged or high cumulative dosing. Chloroquine can cause retinopathy that may be irreversible. Long-term users need baseline and periodic eye exams per specialist guidance. Seek urgent care if you notice blurred vision, difficulty focusing, halos, or changes in color vision.
Other precautions include potential hypoglycemia (which can occur even without diabetes), neuromuscular effects (worsening of myasthenia gravis), seizure risk in susceptible individuals, and caution in hepatic or renal impairment due to altered drug clearance. Use during pregnancy for chloroquine-sensitive malaria prophylaxis and treatment has historically been considered acceptable at recommended doses; nonetheless, all decisions in pregnancy and breastfeeding should be individualized with a clinician.
Chloroquine is contraindicated in individuals with known hypersensitivity to chloroquine or related 4-aminoquinolines. It should generally be avoided in patients with preexisting macular or retinal disease, those with documented QT prolongation or a history of torsades de pointes, and in patients with uncontrolled epilepsy. Severe psoriasis and certain porphyrias may be exacerbated by chloroquine; prescribers weigh risks carefully in these conditions.
Common side effects include nausea, vomiting, abdominal discomfort, decreased appetite, headache, dizziness, and itching (pruritus). Pruritus may be more frequent in some patients and often lessens with continued dosing. Taking chloroquine with food can help reduce gastrointestinal upset.
Less common but more serious effects include cardiotoxicity (QT prolongation, arrhythmias, cardiomyopathy), significant hypoglycemia (sweating, confusion, visual changes), neuropsychiatric symptoms (agitation, mood changes, nightmares), seizures in susceptible individuals, and hematologic abnormalities. Dermatologic reactions, including photosensitivity and rash, can occur; rare severe skin reactions warrant immediate medical attention.
Ocular toxicity presents with blurred vision, scotomas, or changes in color perception and is associated with long-term or high cumulative exposure. Any new visual symptoms require prompt evaluation and discontinuation guidance from a prescriber. If you experience chest pain, fainting, rapid or irregular heartbeat, severe weakness, or sudden visual changes, seek emergency care.
Chloroquine interacts with numerous drugs. Concomitant use with other QT-prolonging agents increases arrhythmia risk. Examples include certain antiarrhythmics (amiodarone, sotalol), macrolide and fluoroquinolone antibiotics (azithromycin, levofloxacin), some antifungals, antipsychotics, methadone, and tricyclic antidepressants. Combining multiple QT-prolonging agents requires careful risk assessment and monitoring.
Absorption can be reduced by antacids containing aluminum or magnesium and by kaolin; separate doses by several hours. Cimetidine may increase chloroquine levels by reducing hepatic metabolism, whereas enzyme inducers such as rifampin may decrease efficacy. Chloroquine can increase plasma concentrations of digoxin and cyclosporine, warranting closer monitoring and possible dose adjustments. Co-administration with antidiabetic medications can potentiate hypoglycemia; patients should monitor glucose and be alert for symptoms.
Using chloroquine with mefloquine may raise seizure risk. When primaquine or tafenoquine is used to prevent P. vivax relapse, clinicians must check G6PD status to prevent hemolysis; while this precaution relates primarily to those agents, overall malaria regimens should be coordinated by a specialist for safety.
If you miss a dose of chloroquine for malaria prophylaxis, take it as soon as you remember unless it is close to the time for your next scheduled dose; do not double up. For treatment regimens with precise timing (e.g., doses at 6, 24, and 48 hours), contact your prescriber for instructions if a dose is missed. Maintaining proper intervals is important to prevent treatment failure.
Chloroquine overdose is a medical emergency with rapid onset of toxicity—particularly dangerous in children due to the drug’s narrow therapeutic index. Early symptoms may include drowsiness, visual disturbances, headache, nausea, and vomiting, quickly progressing to life-threatening hypotension, arrhythmias, seizures, and cardiac arrest. Even small amounts can be fatal; keep tablets in child-resistant containers and out of sight and reach of children.
If an overdose is suspected, call emergency services and your regional poison control center immediately. Do not induce vomiting. Emergency management may require airway protection, aggressive cardiac monitoring, vasopressors, IV diazepam, and correction of electrolytes in a critical care setting.
Store chloroquine at controlled room temperature in a dry place away from excess heat, moisture, and light. Keep it in the original, tightly closed container, and never share the medication. Check expiration dates and properly dispose of unused tablets through take-back programs if available.
In the United States, chloroquine is a prescription-only medication. You cannot legally buy chloroquine without prescription from legitimate pharmacies. This safeguard exists because proper indication, destination-specific resistance patterns, dosing, and safety monitoring (for QT prolongation, interactions, and rare retinal toxicity) require professional evaluation. Avoid online sellers that advertise antimalarials without a prescription—these sources commonly dispense substandard or counterfeit products and can put you at serious risk.
Safe access options include scheduling a visit with a primary care clinician, travel medicine clinic, or infectious diseases specialist, either in person or via telemedicine. These clinicians can confirm whether chloroquine is appropriate for your itinerary (many regions require other agents), arrange vaccines and standby therapy if needed, and counsel you on mosquito-bite prevention. For treatment of suspected malaria, seek urgent medical care rather than self-medicating.
Hospitals and rehabilitation centers, such as HealthSouth Rehabilitation Hospital of Tallahassee, can help coordinate legitimate, clinician-led care pathways. That means a licensed provider evaluates you and, when medically appropriate, authorizes therapy; medications are dispensed under medical orders rather than over the counter. This is not the same as buying chloroquine without a prescription, which is unlawful. Contact qualified healthcare providers to discuss appropriate evaluation and legally obtain any necessary prescriptions.
Chloroquine is an antimalarial medication in the 4-aminoquinoline class that targets malaria parasites in the blood. Because of resistance, its modern use is mainly in areas where Plasmodium species remain chloroquine-sensitive and occasionally for extraintestinal amebiasis; hydroxychloroquine has largely replaced it for autoimmune conditions.
Chloroquine accumulates in the parasite’s acidic food vacuole and inhibits heme detoxification, causing toxic heme buildup that kills the Plasmodium parasite. It also has lysosomotropic and immunomodulatory effects that explain some non-malarial uses.
Chloroquine is used for treatment and prevention of malaria caused by chloroquine-sensitive Plasmodium species (such as many P. vivax and P. ovale strains, P. malariae, and some P. falciparum in limited regions). It may also be used as part of therapy for hepatic amebiasis, usually alongside other agents.
Yes, but selectively. Due to global P. falciparum resistance, chloroquine is not effective in many regions. It remains useful where local surveillance confirms sensitivity, and for certain P. vivax infections where resistance is low.
Avoid chloroquine in people with a known allergy to 4-aminoquinolines and use caution or avoid in those with preexisting retinal disease, significant cardiac conduction disorders or prolonged QT, severe liver or kidney impairment, psoriasis or porphyria, seizure disorders, or myasthenia gravis. A clinician should evaluate risks and benefits.
Common effects include gastrointestinal upset (nausea, abdominal pain), headache, dizziness, blurred vision, and itching. These are usually mild and improve when taken with food, but persistent or severe symptoms warrant medical advice.
Serious risks include retinal toxicity and vision changes with long-term or high cumulative doses, cardiomyopathy and heart rhythm disturbances (including QT prolongation and torsades de pointes), severe hypoglycemia, neuropsychiatric effects, seizures, severe skin reactions, and blood dyscrasias. Urgent care is needed if alarming symptoms appear.
Yes. Chloroquine can prolong the QT interval and trigger dangerous arrhythmias, especially at high doses, in overdose, or when combined with other QT-prolonging drugs or electrolyte disturbances. Patients with cardiac disease or on interacting medications require careful assessment.
Chloroquine has important interactions. Antacids and adsorbents (like kaolin) can reduce absorption; separate dosing by several hours. Many drugs that prolong the QT interval increase arrhythmia risk when combined. Cimetidine may raise chloroquine levels. Insulin and other antidiabetic drugs’ effects can be potentiated, raising hypoglycemia risk. Always provide a full medication list to a clinician or pharmacist.
At standard antimalarial doses, chloroquine is generally considered acceptable during pregnancy and compatible with breastfeeding in settings where it is indicated. Decisions should be guided by local resistance patterns and obstetric advice.
Chloroquine is taken by mouth, typically as a short course for treatment or on a scheduled basis for prevention in chloroquine-sensitive regions. Regimens depend on weight, species, and local guidelines. Do not self-dose; follow a clinician’s instructions and official travel medicine recommendations.
For short-term use in malaria, routine eye screening is usually not necessary. For prolonged therapy or higher cumulative doses, a baseline eye exam and periodic screening are recommended to detect early retinal changes.
No. Large, well-conducted studies show chloroquine (and hydroxychloroquine) does not improve outcomes in COVID-19 and may cause harm. It is not recommended for treating or preventing COVID-19 or other viral illnesses outside clinical trials.
Take the missed dose when remembered unless it is close to the next scheduled dose. Do not double up. Resume the regular schedule and contact a healthcare professional if unsure.
Chloroquine overdose can be rapidly fatal due to profound hypotension, severe hypokalemia, seizures, and malignant arrhythmias. Immediate emergency care is critical; call emergency services and poison control without delay.
Both are 4-aminoquinoline antimalarials with similar mechanisms. Hydroxychloroquine has a hydroxyl group that confers a better safety profile, especially for long-term use in autoimmune diseases like lupus and rheumatoid arthritis. For malaria, both can work where parasites are sensitive, but local guidance determines use.
Hydroxychloroquine is generally safer for chronic therapy, with a lower risk of retinal toxicity at comparable therapeutic exposures and fewer adverse effects overall. When long-term immunomodulation is needed, hydroxychloroquine is usually preferred.
Where Plasmodium falciparum is chloroquine-sensitive, chloroquine can be effective and well tolerated. In most regions with falciparum resistance, quinine (often combined with doxycycline or clindamycin) or, preferably, artemisinin-based combinations are used. Quinine can cause cinchonism (tinnitus, headache, nausea) and other side effects.
Mefloquine is effective in many chloroquine-resistant regions and is dosed weekly, but it can cause neuropsychiatric adverse effects in some people. Chloroquine is also a weekly option but is suitable only in areas with chloroquine-sensitive malaria. Choice depends on resistance maps, medical history, and tolerability.
Chloroquine treats blood-stage parasites. Primaquine targets dormant liver forms (hypnozoites) of P. vivax and P. ovale to prevent relapse and also has gametocidal activity. Primaquine requires G6PD testing to avoid hemolysis. Often, chloroquine is used for the acute blood-stage infection and primaquine is added to prevent relapses where safe.
Both are 4-aminoquinolines with overlapping resistance patterns. Amodiaquine is commonly used in combination regimens (such as artesunate–amodiaquine) for falciparum malaria in some regions. Long-term amodiaquine prophylaxis has been associated with hepatotoxicity and neutropenia, so it is mainly used as part of short-course treatment.
ACTs are the global first-line treatments for uncomplicated P. falciparum malaria because they rapidly clear parasites and overcome resistance. Chloroquine is reserved for areas where parasites remain chloroquine-sensitive, more often with non-falciparum species or specific locales.
Doxycycline is effective in many resistant areas, taken daily, and also protects against some other infections, but it can cause photosensitivity and gastrointestinal irritation. Chloroquine is weekly and inexpensive but is useful only in chloroquine-sensitive regions. Travel medicine advice should be tailored to destination and health profile.
Tafenoquine is a long-acting 8-aminoquinoline used as a single-dose radical cure for P. vivax hypnozoites and for prophylaxis. It requires quantitative G6PD testing due to hemolysis risk and has a long half-life. Chloroquine treats blood stages but does not eradicate hypnozoites.
Both face significant resistance. SP remains in use for intermittent preventive treatment in pregnancy (IPTp) in some regions with specific guidelines. Chloroquine is used where sensitivity persists, more commonly for non-falciparum malaria. Local resistance data and national policies drive selection.
For malaria treatment or prophylaxis in areas with chloroquine-sensitive parasites, chloroquine may be chosen. For autoimmune conditions, hydroxychloroquine is generally preferred due to better safety, with chloroquine reserved for specific circumstances and close monitoring.
Effectiveness against local strains, dosing convenience, side-effect profiles, contraindications (such as psychiatric history for mefloquine), and cost all matter. Chloroquine is only suitable where parasites are sensitive; atovaquone–proguanil is well tolerated with daily dosing but tends to be more expensive.
No. Intravenous artesunate is the treatment of choice for severe malaria in modern guidelines. Chloroquine is not appropriate for severe disease and is ineffective against resistant falciparum strains.
Chloroquine is inexpensive and widely available as a generic, but its clinical utility is limited by resistance. ACTs and some newer agents can cost more but are prioritized for efficacy. Hydroxychloroquine is widely available for rheumatologic indications, often at modest cost.
Both can cause retinopathy, particularly with long-term use and high cumulative doses, but hydroxychloroquine has a lower risk at recommended dosing. Regular ophthalmologic monitoring is more critical when long-term therapy is required, especially with chloroquine.