|Trade names||Plaquenil, others|
|Other names||Hydroxychloroquine sulfate, HCQ|
|Main uses||Prevent and treat chloroquine sensitive malaria, rheumatoid arthritis, lupus, porphyria cutanea tarda|
|Side effects||Vomiting, headache, changes in vision, muscle weakness|
|By mouth (tablets)|
|Defined daily dose||0.5 gram ( by mouth)|
|Bioavailability||Variable (74% on average); Tmax = 2–4.5 hours|
|Elimination half-life||32–50 days|
|Excretion||Mostly kidney (23–25% as unchanged drug), also biliary (<10%)|
|Chemical and physical data|
|Molar mass||335.88 g·mol−1|
|3D model (JSmol)|
|(what is this?)|
Hydroxychloroquine (HCQ), sold under the brand name Plaquenil among others, is a medication used to prevent and treat malaria in areas where malaria remains sensitive to chloroquine. Other uses include treatment of rheumatoid arthritis, lupus, and porphyria cutanea tarda. It is taken by mouth. HCQ is not recommended in coronavirus disease 2019 (COVID‑19). High quality evidence of benefit for such use is lacking, with concerns of potential harms from side effects.
Common side effects may include vomiting, headache, changes in vision, and muscle weakness. Severe side effects may include allergic reactions, vision problems, and heart problems. Monitoring for eye problems is recommended before starting and then regularly thereafter. Although all risk cannot be excluded, it remains a treatment for rheumatic disease during pregnancy. In overdose it can be life-threatening. Hydroxychloroquine is in the antimalarial and 4-aminoquinoline families of medication.
Hydroxychloroquine was approved for medical use in the United States in 1955. It is on the World Health Organization's List of Essential Medicines. In 2017, it was the 128th most commonly prescribed medication in the United States, with more than five million prescriptions. A typical dose is between 200 - 400mg per day by mouth. The speculative use of hydroxychloroquine for COVID‑19 threatens its availability for people with established indications.
Hydroxychloroquine is an immunosuppressive and mild immunomodulatory agent also known as a conventional disease modifying anti-rheumatic drug (DMARD). It was developed as a medication to treat malaria and is primarily used in the treatment of rheumatoid arthritis and lupus, often combined with other medications.
Hydroxychloroquine can be used as a DMARD in some autoimmune conditions such as systemic lupus erythematosus and rheumatoid arthritis, but must not be used in psoriatic arthropathy where it may worsen the psoriasis rash. Around half of people treated with hydroxychloroquine for rheumatic disease will respond with a beneficial effect, which may not be noticed until at least a month or two after starting the medication. It is considered the first-line treatment for cutaneous lupus erythematosus.
It is widely used to treat primary Sjögren syndrome but does not appear to be effective in controlling the associated dry eyes and mouth. However, hydroxychloroquine may help with the associated joint pains and tiredness.
Where there is no chloroquine-resistance, hydroxychloroquine can be used to prevent and treat malaria, such as caused by Plasmodium malariae and Plasmodium ovale. Plasmodium vivax may not always be chloroquine-susceptible. Plasmodium falciparum is usually resistant to hydroxychloroquine and requires an alternative medication. Malaria associated with complications may require different or additional medication. If a person is already taking hydroxychloroquine for another indication, but requires chloroquine to prevent malaria, they can remain on the hydroxychloroquine.
The drug label advises that hydroxychloroquine should not be prescribed to individuals with known hypersensitivity to 4-aminoquinoline compounds. There are several other contraindications, and caution is required if the person considered for treatment has certain heart conditions, diabetes, or psoriasis.
Side effects from hydroxychloroquine are more common with long-term use and are related to the dose and level in blood. The most common side effects are nausea, stomach cramps, and diarrhea. Other common side effects include itching and headache. The most serious side effects affect the eye, with dose-related retinopathy as a concern even after hydroxychloroquine use is discontinued. Retinopathy has been found to be more common than previously thought and monitoring is recommended before starting hydroxychloroquine and then regularly thereafter. Compared to other conventional DMARDs, hydroxychloroquine has a good safety record, and does not cause liver or kidney problems, or increase the risk severe infections.
Serious reported neuropsychiatric adverse effects of hydroxychloroquine use include agitation, mania, difficulty sleeping, hallucinations, psychosis, catatonia, paranoia, depression, and suicidal thoughts. In rare situations, hydroxychloroquine has been implicated in cases of serious skin reactions such as Stevens–Johnson syndrome, toxic epidermal necrolysis, and Drug reaction with eosinophilia and systemic symptoms. Reported blood abnormalities with its use include lymphopenia, eosinophilia, and atypical lymphocytosis.
For short-term treatment of acute malaria, adverse effects can include abdominal cramps, diarrhea, heart problems, reduced appetite, headache, nausea and vomiting. Other adverse effects noted with short-term use of Hydroxychloroquine include low blood sugar and QT interval prolongation. Idiosyncratic hypersensitivity reactions have occurred.
For prolonged treatment of lupus or rheumatoid arthritis, adverse effects include the acute symptoms, plus altered eye pigmentation, acne, anemia, bleaching of hair, blisters in mouth and eyes, blood disorders, cardiomyopathy, convulsions, vision difficulties, diminished reflexes, emotional changes, excessive coloring of the skin, hearing loss, hives, itching, liver problems or liver failure, loss of hair, muscle paralysis, weakness or atrophy, nightmares, psoriasis, reading difficulties, tinnitus, skin inflammation and scaling, skin rash, vertigo, weight loss, and occasionally urinary incontinence. Hydroxychloroquine can worsen existing cases of both psoriasis and porphyria.
Children may be especially vulnerable to developing adverse effects from hydroxychloroquine.
One of the most serious side effects is retinopathy (generally with chronic use). People taking 400 mg of hydroxychloroquine or less per day generally have a negligible risk of macular toxicity, whereas the risk begins to increase when a person takes the medication over five years or has a cumulative dose of more than 1000 grams. The daily safe maximum dose for eye toxicity can be computed from a person's height and weight. Macular toxicity is related to the total cumulative dose rather than the daily dose. Regular eye screening, even in the absence of visual symptoms, is recommended to begin when either of these risk factors occurs.
Toxicity from hydroxychloroquine may be seen in two distinct areas of the eye: the cornea and the macula. The cornea may become affected (relatively commonly) by an innocuous cornea verticillata or vortex keratopathy and is characterized by whorl-like corneal epithelial deposits. These changes bear no relationship to dosage and are usually reversible on cessation of hydroxychloroquine.
The macular changes are potentially serious. Advanced retinopathy is characterized by reduction of visual acuity and a "bull's eye" macular lesion which is absent in early involvement.
In overdose, Hydroxychloroquine can be life-threatening. This may be preceded by an incontrollable convulsions or the rapid onset of an irregular heart beat. Serious symptoms of overdose generally occur within an hour of ingestion. These symptoms may include sleepiness, vision changes, seizures, coma, stopping of breathing, and heart problems such as ventricular fibrillation and low blood pressure. Loss of vision may be permanent. Low blood potassium, to levels of 1 to 2 mmol/L, may also occur. Cardiovascular abnormalities such as QRS complex widening and QT interval prolongation may also occur.
Chloroquine has a risk of death in overdose in adults of about 20%, while hydroxychloroquine is estimated to be two or threefold less toxic. While overdoses of hydroxychloroquine have historically been uncommon, one report documented three deaths out of eight cases.
Treatment recommendations include early mechanical ventilation, heart monitoring, and activated charcoal. Supportive treatment with intravenous fluids and vasopressors may be required with epinephrine being the vasopressor of choice. Stomach pumping may also be used. Sodium bicarbonate and hypertonic saline may be used in cases of severe QRS complex widening. Seizures may be treated with benzodiazepines. Intravenous potassium chloride may be required, however this may result in high blood potassium later in the course of the disease. Dialysis does not appear to be useful.
Hydroxychloroquine may be quantified in plasma or serum to confirm a diagnosis of poisoning in hospitalized victims or in whole blood to assist in a forensic investigation of a case of sudden or unexpected death. Plasma or serum concentrations are usually in a range of 0.1-1.6 mg/L during therapy and 6–20 mg/L in cases of clinical intoxication, while blood levels of 20–100 mg/L have been observed in deaths due to acute overdosage.
The concurrent use of hydroxychloroquine and the antibiotic azithromycin appears to increase the risk for certain serious side effects with short-term use, such as an increased risk of chest pain, congestive heart failure, and mortality from cardiovascular causes. Care should be taken if combined with medication altering liver function as well as aurothioglucose (Solganal), cimetidine (Tagamet) or digoxin (Lanoxin). Hydroxychloroquinecan increase plasma concentrations of penicillamine which may contribute to the development of severe side effects. It enhances hypoglycemic effects of insulin and oral hypoglycemic agents. Dose altering is recommended to prevent profound hypoglycemia. Antacids may decrease the absorption of hydroxychloroquine. Both neostigmine and pyridostigmine antagonize the action of hydroxychloroquine.
- Digoxin (wherein it may result in increased serum digoxin levels)
- Insulin or anti-diabetic medication (wherein it may enhance the effects of a hypoglycemic treatment)
- Drugs that prolong QT interval and other arrhythmogenic drugs (as Hydroxychloroquine prolongs the QT interval and may increase the risk of inducing serious abnormal heart rhythms (ventricular arrhythmias) if used concurrently)
- Mefloquine and other drugs known to lower the seizure threshold (co-administration with other antimalarials known to lower the convulsion threshold may increase risk of convulsions)
- Antiepileptics (concurrent use may impair the antiepileptic activity)
- Methotrexate (combined use is unstudied and may increase the frequency of side effects)
- Cyclosporin (wherein an increased plasma cyclosporin level was reported when used together).
Hydroxychloroquine has similar pharmacokinetics to chloroquine, with rapid gastrointestinal absorption, large distribution volume, and elimination by the kidneys. Cytochrome P450 enzymes (CYP2D6, 2C8, 3A4 and 3A5) metabolize hydroxychloroquine to N-desethylhydroxychloroquine. Both agents also inhibit CYP2D6 activity and may interact with other medications that depend on this enzyme.
Antimalarials are lipophilic weak bases and easily pass plasma membranes. The free base form accumulates in lysosomes (acidic cytoplasmic vesicles) and is then protonated, resulting in concentrations within lysosomes up to 1000 times higher than in culture media. This increases the pH of the lysosome from four to six. Alteration in pH causes inhibition of lysosomal acidic proteases causing a diminished proteolysis effect. Higher pH within lysosomes causes decreased intracellular processing, glycosylation and secretion of proteins with many immunologic and nonimmunologic consequences. These effects are believed to be the cause of a decreased immune cell functioning such as chemotaxis, phagocytosis and superoxide production by neutrophils. Hydroxychloroquine is a weak diprotic base that can pass through the lipid cell membrane and preferentially concentrate in acidic cytoplasmic vesicles. The higher pH of these vesicles in macrophages or other antigen-presenting cells limits the association of autoantigenic (any) peptides with class II MHC molecules in the compartment for peptide loading and/or the subsequent processing and transport of the peptide-MHC complex to the cell membrane.
Mechanism of action
Its mechanism of action is not fully understood. lysosomal pH in antigen-presenting cells. In inflammatory conditions, it blocks toll-like receptors on plasmacytoid dendritic cells (PDCs). Toll-like receptor 9 (TLR 9), which recognizes DNA-containing immune complexes, leads to the production of interferon and causes the dendritic cells to mature and present antigen to T cells. Hydroxychloroquine, by decreasing TLR signaling, reduces the activation of dendritic cells and the inflammatory process.[medical citation needed]
In 2003, a novel mechanism was described wherein hydroxychloroquine inhibits stimulation of the toll-like receptor (TLR) 9 family receptors. TLRs are cellular receptors for microbial products that induce inflammatory responses through activation of the innate immune system.
As with other quinoline antimalarial drugs, the antimalarial mechanism of action of quinine has not been fully resolved. The most accepted model is based on hydrochloroquinine and involves the inhibition of hemozoin biocrystallization, which facilitates the aggregation of cytotoxic heme. Free cytotoxic heme accumulates in the parasites, causing death.
Hydroxychloroquine increases the risk of low blood sugar through several mechanisms. These include decreased clearance of the hormone insulin from the blood, increased insulin sensitivity, and increased release of insulin from the pancreas.
Hydroxychloroquine was first developed for use in malaria, before it was found more effective in lupus and rheumatoid arthritis. That an antimalarial drug might treat conditions other than malaria first came to recognition when Payne reported that quinine could cure cutaneous lupus in 1894. Chloroquine had been produced in 1934 by the Germans, but its toxic effect in bird models led to its abandonment. During the Second World War, it was noted that soldiers who took antimalarials were often relieved of rashes and inflammatory arthritis. This led to the first trial that showed these drugs may have some use in SLE. To reduce toxicity whilst maintaining efficacy, hydroxychloroquine, which differs from chloroquine by a hydroxyl group, was introduced in 1955, when it was approved for medical use in the United States. By using it in combination with other medications, potential toxicity and side effects were reduced further. Since the 1990s, reports of its effects in several infections including influenza A and B, H5N1, HIV, hepatitis A and C, Lassa fever, and ebola, have been published.
Society and culture
Hydroxychloroquine is relatively cheap and is on the World Health Organization's List of Essential Medicines.
The wholesale cost in the developing world was about US$4.65 per month as of 2015[update], when used for rheumatoid arthritis or lupus. In the United States the wholesale cost of a month of treatment is about US$25 as of 2020[update]. In the United Kingdom a dose of 400mg/day by mouth costs the National Health Service £5.79.
Brand names of hydroxychloroquine include Plaquenil, Hydroquin, Axemal (in India), Dolquine, Quensyl, Quinoric.
Beginning in March 2020, US President Donald Trump began promoting hydroxychloroquine to prevent or treat COVID-19, citing small numbers of anecdotal reports. Trump stated in June that he was taking the drug as a preventive measure, stimulating unprecedented worldwide demand and causing shortages of hydroxychloroquine for its prescribed purpose of preventing malaria.
After issuing an emergency use authorization for physicians to use the drug to treat hospitalized people with severe COVID-19 infection, the US Food and Drug Administration withdrew the authorization in June after finding hydroxychloroquine was unlikely to be effective and had serious side effects. During ensuing months, additional studies found the drug was not effective, and in late July, Anthony Fauci stated, "We know that every single good study — and by good study I mean randomized controlled study in which the data are firm and believable — has shown that hydroxychloroquine is not effective in the treatment of COVID-19."
There is no strong scientific evidence to support the use of hydroxychloroquine for preventing or treating coronavirus disease 2019 (COVID‑19). While its use is not approved by the FDA for COVID‑19 treatment, from April to June 2020, there was an emergency use authorization for its use in the United States, and it has been used off label for potential treatment of the disease. On 24 April 2020, citing the risk of "serious heart rhythm problems", the FDA posted a caution against using the drug for COVID‑19 "outside of the hospital setting or a clinical trial". On 15 June, the FDA revoked its emergency use authorization, stating that it was "no longer reasonable to believe" that the drug was effective against COVID-19 or that its benefits outweighed "known and potential risks".
A randomized, double-blind, placebo-controlled study of hydroxychloroquine in 821 participants found that it did not treat COVID‑19 infection, although the study had limitations. In June, use of hydroxychloroquine in the UK RECOVERY Trial was discontinued when an interim analysis of 1,542 treatments showed it provided no mortality benefit to people with severe COVID-19 infection hospitalized over 28 days.
On 17 March 2020, Didier Raoult announced in an online video that a trial involving 24 patients from southeast France supported the claim that hydroxychloroquine and azithromycin were effective in treating for COVID-19. On 20 March, he published a preliminary report of his study online in the International Journal of Antimicrobial Agents. A later peer review found the study was “irresponsible.”
On 17 March 2020, the AIFA Scientific Technical Commission of the Italian Medicines Agency expressed a favorable opinion on including the off-label use of chloroquine and hydroxychloroquine for the treatment of COVID‑19.
During a press briefing on 19 March 2020, Donald Trump, the President of the United States, promoted the drugs chloroquine and hydroxychloroquine as a potential treatment for COVID‑19. Trump claimed that chloroquine had been "approved very, very quickly" by the US Food and Drug Administration (FDA) while discussing treatments for COVID‑19. The FDA later said it had not given approval for the drug to be used in treatment of COVID‑19, but was now allowing chloroquine under compassionate use guidelines. Trump's remarks led to a shortage of chloroquine and hydroxychloroquine in the United States and panic-buying in Africa and South Asia.
In the United States in March 2020, several state pharmacy boards reported that some doctors and dentists were writing prescriptions for hydroxychloroquine and a related drug, chloroquine, to themselves, family members, and staff. Sudden demand spikes caused by hospital use for severely ill COVID‑19 patients and prescriptions for prophylaxis have resulted in shortages; doctors have expressed concern that patients who have long taken hydroxychloroquine for other approved indications, like lupus and rheumatoid arthritis, will be unable to procure needed medicine.
News outlets reported on 24 March 2020 that, in the state of Arizona, a man had died, leaving his wife in critical condition, as a result of ingesting a product containing chloroquine phosphate designed for treating sick fish. The couple believed the fish treatment could prevent them from contracting COVID‑19. Although chloroquine phosphate is a related compound to hydroxychloroquine, unlike hydroxychloroquine it is used for the treatment of fish parasites and infections. It has a different chemical structure from chloroquine and hydroxychloroquine which, when used in humans and other animals, could result in death.
In early April 2020, a Texas nursing home administered hydroxychloroquine to dozens of residents who had COVID-19. The facility's medical director, Dr. Robin Armstrong, acquired the drug through his connections to the Republican Party; he made the request through Texas Lt. Gov. Dan Patrick.
On 28 March 2020, the FDA issued an emergency use authorization (EUA) to allow hydroxychloroquine sulfate and chloroquine phosphate products donated to the Strategic National Stockpile (SNS) to be distributed and used for certain people who are hospitalized with COVID‑19. In anticipation of product shortages, the FDA issued product-specific guidance for chloroquine phosphate and for hydroxychloroquine sulfate for generic drug manufacturers. On 24 April 2020, "due to risk of heart rhythm problems", the FDA cautioned the use of hydroxychloroquine or chloroquine for COVID‑19 outside of the hospital setting or a clinical trial.
On 29 April 2020, based on a preprint retrospective cohort study posted 10 April 2020, on medRxiv of more than 320,000 individuals that were not infected with COVID‑19, but had been treated with a combination of both hydroxychloroquine and azithromycin, an article published in The FASEB Journal cautioned against this combination to treat patients with COVID‑19 outside the context of a clinical trial. This was due to safety concerns with this combination and lack of evidence showing benefit to combining these medications. However the article suggested the combination could be used to treat COVID‑19 patients if new strong scientific evidence showed that combination as beneficial, there is no alternative treatment available, and the patients are counselled and closely monitored.
Based on the results of a study published in The Lancet (which was retracted on 4 June 2020)  the World Health Organization suspended hydroxychloroquine from its global drug trials for COVID‑19 treatments on 26 May 2020, due to safety concerns in that study. It had previously enrolled 3,500 patients from 17 countries in the Solidarity Trial, which was the official name of its study of hydroxychloroquine against COVID‑19. Due to the increased risks described in a subsequently retracted study, France, Italy and Belgium banned the use of hydroxychloroquine as a COVID‑19 treatment. None of the results used as the basis of these bans involved outpatient treatment. The first results for outpatient clinical trials of hydroxychloroquine with azithromycin are expected in September 2020.
On 29 May 2020, the EMA issued a public health statement reminding healthcare professionals to closely monitor people with COVID‑19 who are receiving hydroxychloroquine.
On 3 June 2020, the WHO announced it would resume its global trial of hydroxychloroquine, after its data safety monitoring committee found there was no increased risk of death for COVID‑19 patients taking it.
On 4 June 2020, an article about the treatment of COVID‑19 patients using hydroxychloroquine with or without macrolides that had been published in The Lancet on 22 May 2020, was retracted by its authors. Before its retraction it had claimed that hospitalized COVID‑19 patients treated with hydroxychloroquine or chloroquine (with or without a macrolide) did not benefit from the treatment, but instead were at greater risk of death. However, since its publication questions were raised about the accuracy of the data used in the article, prompting a third party review which resulted in the retraction of the article from the journal.
On 5 June 2020, Peter Horby, Professor of Emerging Infectious Diseases and Global Health in the Nuffield Department of Medicine, University of Oxford, and chief investigator for a randomised trial on hydroxychloroquine, said: "the RECOVERY Trial has shown that hydroxychloroquine is not an effective treatment in patients hospitalised with COVID-19".
On 15 June 2020, the FDA revoked the emergency use authorization for hydroxychloroquine and chloroquine. The FDA also updated the fact sheets for the emergency use authorization of remdesivir, to warn that using chloroquine or hydroxychloroquine with remdesivir may reduce the antiviral activity of remdesivir.
- "Hydroxychloroquine Sulfate Monograph for Professionals". The American Society of Health-System Pharmacists. 20 March 2020. Archived from the original on 20 March 2020. Retrieved 20 March 2020.
- "Hydroxychloroquine Use During Pregnancy". Drugs.com. 28 February 2020. Retrieved 21 March 2020.
- "WHOCC - ATC/DDD Index". www.whocc.no. Retrieved 16 September 2020.
- Lamontagne, François; Agoritsas, Thomas; Siemieniuk, Reed (2 March 2021). "A living WHO guideline on drugs to prevent covid-19". BMJ. 372. doi:10.1136/bmj.n526.
- "COVID-19 Mythbusters – World Health Organization". www.who.int. Retrieved 2 March 2021.
- Meyerowitz EA, Vannier AG, Friesen MG, Schoenfeld S, Gelfand JA, Callahan MV, et al. (May 2020). "Rethinking the role of hydroxychloroquine in the treatment of COVID-19". FASEB Journal. 34 (5): 6027–6037. doi:10.1096/fj.202000919. PMID 32350928.
- Cortegiani A, Ingoglia G, Ippolito M, Giarratano A, Einav S (June 2020). "A systematic review on the efficacy and safety of chloroquine for the treatment of COVID-19". Journal of Critical Care. 57: 279–283. doi:10.1016/j.jcrc.2020.03.005. PMID 32173110.
- "Guidance on patients at risk of drug-induced sudden cardiac death from off-label COVID-19 treatments". newsnetwork.mayoclinic.org. 25 March 2020.
- BNF (80 ed.). BMJ Group and the Pharmaceutical Press. September 2021 – March 2021. p. 1156-1157. ISBN 978-0-85711-369-6.
- Flint J, Panchal S, Hurrell A, van de Venne M, Gayed M, Schreiber K, et al. (September 2016). "BSR and BHPR guideline on prescribing drugs in pregnancy and breastfeeding—Part I: standard and biologic disease modifying anti-rheumatic drugs and corticosteroids". Rheumatology. 55 (9): 1693–7. doi:10.1093/rheumatology/kev404. PMID 26750124.
- World Health Organization (2019). World Health Organization model list of essential medicines: 21st list 2019. Geneva: World Health Organization. hdl:10665/325771. WHO/MVP/EMP/IAU/2019.06. License: CC BY-NC-SA 3.0 IGO.
- "The Top 300 of 2020". ClinCalc. Retrieved 18 March 2020.
- "Hydroxychloroquine Sulfate – Drug Usage Statistics". ClinCalc. Retrieved 7 April 2020.
- Benjamin, Onecia; Bansal, Pankaj; Goyal, Amandeep; Lappin, Sarah L. (2020). "Disease Modifying Anti-Rheumatic Drugs (DMARD)". StatPearls. StatPearls Publishing.
- Butrous, Ghazwan (22 January 2021). "The 500 years story of hydroxychloroquine and its implication on our medical knowledge: From Malaria to COVID-19". Interdisciplinary Approaches to Medicine. 1 (2): 3–13. doi:10.26577/IAM.2020.v1.i2.01.
- Ritter, James M.; Flower, Rod J.; Henderson, Graeme; Loke, Yoon Kong; MacEwan, David; Rang, Humphrey P. (2020). "27. Anti-inflammatory and immunosuppressant drugs". Rang & Dale's Pharmacology. Elsevier. p. 353. ISBN 978-0-7020-7448-6.
- Chong, Benjamin F.; Werth, Victoria P. (2018). "58. Management of cutaneous lupus erythematosis". In Wallace, Daniel; Hahn, Bevra Hannahs (eds.). Dubois' Lupus Erythematosus and Related Syndromes - E-Book. Elsevier Health Sciences. p. 719. ISBN 978-0-323-55064-2.
- Wang SQ, Zhang LW, Wei P, Hua H (May 2017). "Is hydroxychloroquine effective in treating primary Sjogren's syndrome: a systematic review and meta-analysis". BMC Musculoskeletal Disorders. 18 (1): 186. doi:10.1186/s12891-017-1543-z. PMC 5427554. PMID 28499370.
- Rahman, Anisur; Giles, Ian (2020). "18. Rheumatology". In Feather, Adam; Randall, David; Waterhouse, Mona (eds.). Kumar and Clark's Clinical Medicine (10th ed.). Elsevier. p. 463. ISBN 978-0-7020-7870-5.
- BNF (80 ed.). BMJ Group and the Pharmaceutical Press. September 2021 – March 2021. p. 643. ISBN 978-0-85711-369-6.
- Halperin, John J. (2011). Lyme Disease: An Evidence-Based Approach. CABI. p. 200. ISBN 978-1-84593-804-8.
- "Plaquenil- hydroxychloroquine sulfate tablet". DailyMed. 3 January 2020. Retrieved 20 March 2020.
- "Plaquenil (hydroxychloroquine sulfate) dose, indications, adverse effects, interactions". pdr.net. Retrieved 19 March 2020.
- "Drugs & Medications". webmd.com. Retrieved 19 March 2020.
- Flach AJ (2007). "Improving the risk-benefit relationship and informed consent for patients treated with hydroxychloroquine". Transactions of the American Ophthalmological Society. 105: 191–4, discussion 195–7. PMC 2258132. PMID 18427609.
- "Plaquenil Risk Calculators". EyeDock. Retrieved 7 April 2020.
- Marmor MF, Kellner U, Lai TY, Lyons JS, Mieler WF (February 2011). "Revised recommendations on screening for chloroquine and hydroxychloroquine retinopathy" (PDF). Ophthalmology. 118 (2): 415–22. doi:10.1016/j.ophtha.2010.11.017. PMID 21292109.
- Ling Ngan Wong A, Tsz Fung Cheung I, Graham CA (February 2008). "Hydroxychloroquine overdose: case report and recommendations for management". European Journal of Emergency Medicine. 15 (1): 16–8. doi:10.1097/MEJ.0b013e3280adcb56. PMID 18180661. S2CID 41205035.
- Smith ER, Klein-Schwartz W (May 2005). "Are 1-2 dangerous? Chloroquine and hydroxychloroquine exposure in toddlers" (PDF). The Journal of Emergency Medicine. 28 (4): 437–43. doi:10.1016/j.jemermed.2004.12.011. PMID 15837026. Archived from the original (PDF) on 15 April 2020. Retrieved 15 April 2020.
- Roque MR, Foster CS (23 March 2020). "Chloroquine and Hydroxychloroquine Toxicity: Practice Essentials, Background, Pathophysiology". Medscape. Archived from the original on 8 April 2020. Retrieved 7 April 2020.
- Pillay VV (2012). Modern Medical Toxicology (PDF). Jaypee Brothers Publishers. p. 458. ISBN 978-93-5025-965-8.
- Lebin, Jacob A.; LeSaint, Kathy T. (2020). "Brief Review of Chloroquine and Hydroxychloroquine Toxicity and Management". Western Journal of Emergency Medicine. 21 (4): 760–763. doi:10.5811/westjem.2020.5.47810. ISSN 1936-900X. PMID 32726238.
- Aronson, Jeffrey K. (2015). Meyler's Side Effects of Drugs: The International Encyclopedia of Adverse Drug Reactions and Interactions. Elsevier. p. 261. ISBN 978-0-444-53716-4. Unknown parameter
- R. Baselt, Disposition of Toxic Drugs and Chemicals in Man, 12th edition, Biomedical Publications, Foster City, CA, 2020, pp. 1024-1026.
- "Russian Register of Medicines: Plaquenil (hydroxychloroquine) Film-coated Tablets for Oral Use. Prescribing Information". rlsnet.ru (in Russian). Sanofi-Synthelabo. Archived from the original on 16 August 2016. Retrieved 14 July 2016.CS1 maint: unrecognized language (link)
- Mohammad S, Clowse ME, Eudy AM, Criscione-Schreiber LG (March 2018). "Examination of Hydroxychloroquine Use and Hemolytic Anemia in G6PDH-Deficient Patients". Arthritis Care & Research. 70 (3): 481–485. doi:10.1002/acr.23296. PMID 28556555.
- Schrezenmeier E, Dörner T (March 2020). "Mechanisms of action of hydroxychloroquine and chloroquine: implications for rheumatology". Nature Reviews. Rheumatology. 16 (3): 155–166. doi:10.1038/s41584-020-0372-x. PMID 32034323. S2CID 211053837.
- Kalia S, Dutz JP (2007). "New concepts in antimalarial use and mode of action in dermatology". Dermatologic Therapy. 20 (4): 160–74. doi:10.1111/j.1529-8019.2007.00131.x. PMC 7163426. PMID 17970883.
- Kaufmann AM, Krise JP (April 2007). "Lysosomal sequestration of amine-containing drugs: analysis and therapeutic implications". Journal of Pharmaceutical Sciences. 96 (4): 729–46. doi:10.1002/jps.20792. PMID 17117426.
- Ohkuma S, Poole B (July 1978). "Fluorescence probe measurement of the intralysosomal pH in living cells and the perturbation of pH by various agents". Proceedings of the National Academy of Sciences of the United States of America. 75 (7): 3327–31. Bibcode:1978PNAS...75.3327O. doi:10.1073/pnas.75.7.3327. PMC 392768. PMID 28524.
- Ohkuma S, Chudzik J, Poole B (March 1986). "The effects of basic substances and acidic ionophores on the digestion of exogenous and endogenous proteins in mouse peritoneal macrophages". The Journal of Cell Biology. 102 (3): 959–66. doi:10.1083/jcb.102.3.959. PMC 2114118. PMID 3949884.
- Oda K, Koriyama Y, Yamada E, Ikehara Y (December 1986). "Effects of weakly basic amines on proteolytic processing and terminal glycosylation of secretory proteins in cultured rat hepatocytes". The Biochemical Journal. 240 (3): 739–45. doi:10.1042/bj2400739. PMC 1147481. PMID 3493770.
- Hurst NP, French JK, Gorjatschko L, Betts WH (January 1988). "Chloroquine and hydroxychloroquine inhibit multiple sites in metabolic pathways leading to neutrophil superoxide release". The Journal of Rheumatology. 15 (1): 23–7. PMID 2832600.
- Fox R (June 1996). "Anti-malarial drugs: possible mechanisms of action in autoimmune disease and prospects for drug development". Lupus. 5 Suppl 1: S4–10. doi:10.1177/0961203396005001031. PMID 8803903. S2CID 208217074.
- Schrezenmeier E, Dörner T (March 2020). "Mechanisms of action of hydroxychloroquine and chloroquine: implications for rheumatology". Nature Reviews. Rheumatology. 16 (3): 155–166. doi:10.1038/s41584-020-0372-x. PMID 32034323. S2CID 211053837.
- Takeda K, Kaisho T, Akira S (2003). "Toll-like receptors". Annual Review of Immunology. 21: 335–76. doi:10.1146/annurev.immunol.21.120601.141126. PMID 12524386.
- Sullivan DJ (December 2002). "Theories on malarial pigment formation and quinoline action". International Journal for Parasitology. 32 (13): 1645–53. doi:10.1016/S0020-7519(02)00193-5. PMID 12435449.
- Ben-Zvi, Ilan; Kivity, Shaye; Langevitz, Pnina; Shoenfeld, Yehuda (2012). "Hydroxychloroquine: From Malaria to Autoimmunity". Clinical Reviews in Allergy & Immunology. 42 (2): 145–153. doi:10.1007/s12016-010-8243-x. ISSN 1080-0549. PMID 21221847.
- "Single Drug Information" (PDF). International Medical Products Price Guide. Retrieved 31 December 2019.
- "NADAC as of 2019-08-07". Centers for Medicare and Medicaid Services. Retrieved 19 March 2020.
Typical dose is 600mg per day. Costs [$]0.28157 per [daily] dose.…
- "Hydroxychloroquine trade names". Drugs-About.com. Retrieved 18 June 2019.
- Piller, Charles (26 March 2020). "'This is insane!' Many scientists lament Trump's embrace of risky malaria drugs for coronavirus". Science. doi:10.1126/science.abb9021. Retrieved 4 August 2020.
- Lovelace, Jr, Berkeley (15 June 2020). "FDA revokes emergency use of hydroxychloroquine". CNBC.
- "Coronavirus (COVID-19) Update: FDA Revokes Emergency Use Authorization for Chloroquine and Hydroxychloroquine". U.S. Food and Drug Administration (FDA) (Press release). 15 June 2020. Retrieved 15 June 2020.
- "No clinical benefit from use of hydroxychloroquine in hospitalised patients with COVID-19". Recovery Trial, Nuffield Department of Population Health, University of Oxford, UK. 5 June 2020. Retrieved 7 June 2020.
- "Coronavirus: Hydroxychloroquine ineffective says Fauci". BBC News Online. 29 July 2020.
- "Assessment of Evidence for COVID-19-Related Treatments: Updated 4/3/2020". ASHP. Retrieved 7 April 2020.
- Yazdany, J; Kim, AHJ (March 2020). "Use of Hydroxychloroquine and Chloroquine During the COVID-19 Pandemic: What Every Clinician Should Know". Annals of Internal Medicine. 172 (11): M20-1334. doi:10.7326/M20-1334. PMC 7138336. PMID 32232419.
- "Coronavirus Disease 2019 (COVID-19)". Centers for Disease Control and Prevention. 11 February 2020. Retrieved 9 April 2020.
- Kalil AC (March 2020). "Treating COVID-19-Off-Label Drug Use, Compassionate Use, and Randomized Clinical Trials During Pandemics". JAMA. 323 (19): 1897. doi:10.1001/jama.2020.4742. PMID 32208486.
- "FDA cautions against use of hydroxychloroquine or chloroquine for COVID-19 outside of the hospital setting or a clinical trial due to risk of heart rhythm problems". U.S. Food and Drug Administration (FDA). 24 April 2020.
- Berkeley Lovelace Jr (15 June 2020). "FDA revokes emergency use of hydroxychloroquine". CNBC.
- "HCQ and CQ revocation letter" (PDF). U.S. Food and Drug Administration (FDA). 15 June 2020. Retrieved 15 June 2020.
- "Frequently Asked Questions on the Revocation of the Emergency Use Authorization for Hydroxychloroquine Sulfate and Chloroquine Phosphate" (PDF). U.S. Food and Drug Administration (FDA). 15 June 2020. Retrieved 15 June 2020.
- "List of references of observational studies of chloroquine and hydroxychloroquine in COVID-19 patients" (PDF). European Medicines Agency (EMA). 29 May 2020. Retrieved 29 May 2020.
- Boulware DR, Pullen MF, Bangdiwala AS, Pastick KA, Lofgren SM, Okafor EC, et al. (June 2020). "A Randomized Trial of Hydroxychloroquine as Postexposure Prophylaxis for Covid-19". N. Engl. J. Med. doi:10.1056/NEJMoa2016638. PMC 7289276. PMID 32492293. Lay summary.
- Cohen MS (June 2020). "Hydroxychloroquine for the Prevention of Covid-19 - Searching for Evidence". N. Engl. J. Med. doi:10.1056/NEJMe2020388. PMC 7289275. PMID 32492298.
- France, Connexion. "French researcher posts successful Covid-19 drug trial". connexionfrance.com. Retrieved 18 March 2020.
- Gautret, Philippe; et al. (20 March 2020) [Online ahead of print]. "Hydroxychloroquine and azithromycin as a treatment of COVID-19: results of an open-label non-randomized clinical trial". International Journal of Antimicrobial Agents: 105949. doi:10.1016/j.ijantimicag.2020.105949. PMC 7102549. PMID 32205204.
- "Hydroxychloroquine: Europe Turns Away From Doctor Who Championed Drug With 'Irresponsible' Study". 21 July 2020.
- "Azioni intraprese per favorire la ricerca e l'accesso ai nuovi farmaci per il trattamento del COVID-19". Italian Medicines Agency (AIFA) (in italiano). 17 March 2020. Retrieved 18 March 2020.
- Nisen, Max (19 March 2020). "Trump Is Overhyping Unproven Coronavirus Drugs". The Washington Post. Bloomberg. Retrieved 24 March 2020. Unknown parameter
- "Remarks by President Trump, Vice President Pence, and Members of the Coronavirus Task Force in Press Briefing". White House. Retrieved 24 March 2020.
- Dale, Daniel (20 March 2020). "Fact check: Trump wrongly claims FDA 'approved' drug chloroquine to treat the coronavirus". CNN. Retrieved 29 March 2020. Unknown parameter
- Naftulin, Julia (20 March 2020). "The FDA is allowing two drugs to be used for 'compassionate use' to treat the coronavirus. Here's what that means". Business Insider. Retrieved 1 April 2020. Unknown parameter
- Coppock, Kristen (19 March 2020). "FDA Announces Two Drugs Given 'Compassionate Use' Status in Treating COVID-19". Pharmacy Times. Retrieved 1 April 2020. Unknown parameter
- Rowland, Christopher (23 March 2020). "As Trump touts an unproven coronavirus treatment, supplies evaporate for patients who need those drugs". The Washington Post. Retrieved 24 March 2020. Unknown parameter
- Parkinson, Joe; Gauthier-Villars, David (23 March 2020). "Trump Claim That Malaria Drugs Treat Coronavirus Sparks Warnings, Shortages". The Wall Street Journal. Retrieved 26 March 2020. Unknown parameter
- Gabler, Ellen (24 March 2020). "States Say Some Doctors Stockpile Trial Coronavirus Drugs, for Themselves". The New York Times. ISSN 0362-4331. Archived from the original on 24 March 2020. Retrieved 31 March 2020. Unknown parameter
- Torres, Stacy. "Stop hoarding hydroxychloroquine. Many Americans, including me, need it". The Washington Post. Archived from the original on 25 March 2020. Retrieved 31 March 2020. Unknown parameter
- "A man died after ingesting a substance he thought would protect him from coronavirus". NBC News. Retrieved 22 May 2020.
- "FDA Letter to Stakeholders: Do Not Use Chloroquine Phosphate Intended for Fish as Treatment for COVID-19 in Humans". U.S. Food and Drug Administration (FDA). 1 May 2020.
- Romo, Vanessa (10 April 2020). "COVID-19 Patients Given Unproven Drug In Texas Nursing Home In 'Disconcerting' Move". NPR. Retrieved 5 July 2020.
- Denise M Hinton (28 March 2020). "Request for Emergency Use Authorization For Use of Chloroquine Phosphate or Hydroxychloroquine Sulfate Supplied From the Strategic National Stockpile for Treatment of 2019 Coronavirus Disease". U.S. Food and Drug Administration (FDA). Retrieved 30 March 2020.
Having concluded that the criteria for issuance of this authorization under 564(c) of the Act are met, I am authorizing the emergency use of chloroquine phosphate and hydroxychloroquine sulfate, as described in the Scope of Authorization section of this letter (Section II) for treatment of COVID-19 when clinical trials are not available, or participation is not feasible, subject to the terms of this authorization.This article incorporates text from this source, which is in the public domain.
- "Emergency Use Authorization". U.S. Food and Drug Administration (FDA). 29 March 2020. Retrieved 30 March 2020.
On March 28, 2020, FDA issued an EUA to allow hydroxychloroquine sulfate and chloroquine phosphate products donated to the Stategic National Stockpile (SNS) to be distributed and used for certain hospitalized patients with COVID-19. These drugs will be distributed from the SNS to states for doctors to prescribe to adolescent and adult patients hospitalized with COVID-19, as appropriate, when a clinical trial is not available or feasible.This article incorporates text from this source, which is in the public domain.
- "Product-Specific Guidances for Chloroquine Phosphate and Hydroxychloro". U.S. Food and Drug Administration (FDA). 13 April 2020. Retrieved 13 April 2020.
- "Trump says he takes unproven hydroxychloroquine to prevent coronavirus infection". CNBC. Retrieved 25 May 2020.
- Mehra MR, Desai SS, Ruschitzka F, Patel AN (May 2020). "Hydroxychloroquine or chloroquine with or without a macrolide for treatment of COVID-19: a multinational registry analysis". Lancet. doi:10.1016/S0140-6736(20)31180-6. PMC 7255293. PMID 32450107. Lay summary. (Retracted, see doi:10.1016/S0140-6736(20)31324-6, )
- Mehra MR, Ruschitzka F, Patel AN (June 2020). "Retraction: "Hydroxychloroquine or chloroquine with or without a macrolide for treatment of COVID-19: a multinational registry analysis"". Lancet. 395 (10240): 1820. doi:10.1016/S0140-6736(20)31324-6. PMC 7274621. PMID 32511943.
- Boseley, Sarah; Davey, Melissa (4 June 2020). "Covid-19: Lancet retracts paper that halted hydroxychloroquine trials". The Guardian. Retrieved 4 June 2020. Unknown parameter
- "Citing safety concerns, the W.H.O. paused tests of a drug Trump said he had taken". The New York Times. 26 May 2020.
- "France bans use of hydroxychloroquine, drug touted by Trump, in coronavirus patients". CBS News. 27 May 2020.
- Beaubien, Jason (25 May 2020). "WHO Halts Hydroxychloroquine Trial Over Safety Concerns". NPR. Retrieved 27 May 2020. Unknown parameter
- Chappell, Bill (27 May 2020). "France Bars Use Of Hydroxychloroquine In COVID-19 Cases". NPR. Retrieved 27 May 2020. Unknown parameter
- Risch, Harvey A. (27 May 2020). "Early Outpatient Treatment of Symptomatic, High-Risk Covid-19 Patients that Should be Ramped-Up Immediately as Key to the Pandemic Crisis". American Journal of Epidemiology. doi:10.1093/aje/kwaa093. PMID 32458969. S2CID 218909081.
- "COVID-19: reminder of the risks chloroquine and hydroxychloroquine". European Medicines Agency (EMA). 29 May 2020. Retrieved 29 May 2020.
- Davey, Melissa; Kirchgaessner, Stephanie; Boseley, Sarah (3 June 2020). "Surgisphere: governments and WHO changed Covid-19 policy based on suspect data from tiny US company". The Guardian. Retrieved 4 June 2020. Unknown parameter
- Horby, Peter; Landray, Martin (5 June 2020). "No clinical benefit from use of hydroxychloroquine in hospitalised patients with COVID-19 — RECOVERY Trial". www.recoverytrial.net. Retrieved 6 June 2020.
- "EUA Archive". U.S. Food and Drug Administration (FDA). 15 June 2020. Retrieved 15 June 2020.
On June 15, 2020, based on FDA's continued review of the scientific evidence available for hydroxychloroquine sulfate (HCQ) and chloroquine phosphate (CQ) to treat COVID-19, FDA has determined that the statutory criteria for EUA as outlined in Section 564(c)(2) of the Food, Drug, and Cosmetic Act are no longer met. Specifically, FDA has determined that CQ and HCQ are unlikely to be effective in treating COVID-19 for the authorized uses in the EUA. Additionally, in light of ongoing serious cardiac adverse events and other serious side effects, the known and potential benefits of CQ and HCQ no longer outweigh the known and potential risks for the authorized use. This warrants revocation of the EUA for HCQ and CQ for the treatment of COVID-19.This article incorporates text from this source, which is in the public domain.
- "Coronavirus (COVID-19) Update: FDA Warns of Newly Discovered Potential Drug Interaction That May Reduce Effectiveness of a COVID-19 Treatment Authorized for Emergency Use". U.S. Food and Drug Administration (FDA) (Press release). 15 June 2020. Retrieved 15 June 2020. This article incorporates text from this source, which is in the public domain.
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