Mefloquine

Pharmacologic Category

Antimalarial Agent

Dosing: Adult

Malaria: Oral (dose expressed as mg of mefloquine hydrochloride):

Mild-to-moderate, treatment: 1,250 mg (5 tablets) as a single dose. Note: If clinical improvement is not seen within 48 to 72 hours, an alternative therapy should be used for re-treatment.

Uncomplicated, treatment (off-label dose): 750 mg (3 tablets) as initial dose, followed 6 to 12 hours later by 500 mg (2 tablets) (CDC 2013b)

Uncomplicated, chloroquine-resistant P. vivax malaria treatment (off-label use): 750 mg (3 tablets) as initial dose, followed 6 to 12 hours later by 500 mg (2 tablets) with concomitant primaquine (CDC 2013b)

Chemoprophylaxis: 250 mg weekly starting 1 week (CDC 2014: ≥2 weeks) before arrival in endemic area, continuing weekly during travel and for 4 weeks after leaving endemic area. Note: Prophylaxis may begin 2 to 3 weeks prior to travel to ensure tolerance.

* See Dosage and Administration in AHFS Essentials for additional information.

Dosing: Geriatric

Refer to adult dosing.

Dosing: Renal Impairment: Adult

No dosage adjustment necessary; only a small amount of mefloquine is renally eliminated.

Dosing: Hepatic Impairment: Adult

There are no dosage adjustments provided in the manufacturer's labeling; however, half-life may be prolonged and plasma levels may be higher in patients with hepatic impairment.

Dosing: Pediatric

Note: Dose is expressed in terms of the salt, mefloquine hydrochloride. Due to geographical resistance and cross-resistance, consult current CDC or WHO guidelines as appropriate.

Malaria, treatment; chloroquine-resistant (independent of HIV status): Note: Therapy is recommended as a last-line option due to higher rate of severe neuropsychiatric reactions; consider other treatment regimens first (CDC 2013):

CDC Guidelines (CDC 2013; HHS [pediatric OI 2017]): Infants, Children, and Adolescents: Oral: 15 mg/kg once (maximum dose: 750 mg/dose) followed in 6 to 12 hours with 10 mg/kg once (maximum dose: 500 mg/dose); use in combination with other anti-malarial agents (refer to local resistance patterns and guidelines); if clinical improvement is not seen within 48 to 72 hours, an alternative therapy should be used for retreatment

Malaria; chemoprophylaxis (independent of HIV status): Note: Begin ≥2 weeks before arrival in endemic area, administer on the same day each week, and continue weekly during travel and for 4 weeks after leaving endemic area (CDC 2018). Infants, Children, and Adolescents:

Weight-based dosing: Oral: 5 mg/kg/dose once weekly; maximum dose: 250 mg/dose (CDC 2018; HHS [pediatric OI 2017])

Fixed dosing (CDC 2018): Oral:

>9 to 19 kg: 62.5 mg (¹/₄ of 250 mg tablet) once weekly

>19 to 30 kg: 125 mg (¹/₂ of 250 mg tablet) once weekly

>30 to 45 kg: 187.5 mg (³/₄ of a 250 mg tablet) once weekly

>45 kg: 250 mg once weekly

Dosing: Renal Impairment: Pediatric

No dosage adjustment necessary; only a small amount of mefloquine is renally eliminated; not removed by hemodialysis.

Dosing: Hepatic Impairment: Pediatric

There are no dosage adjustments provided in the manufacturer's labeling; however, half-life may be prolonged and plasma levels may be higher in patients with hepatic impairment; use with caution.

Use: Labeled Indications

Acute malaria infections: Treatment of mild to moderate acute malaria caused by mefloquine-susceptible strains of Plasmodium falciparum (both chloroquine-susceptible and -resistant strains) or by Plasmodium vivax.

Prophylaxis of malaria: Prophylaxis of P. falciparum and P. vivax malaria infections, including prophylaxis of chloroquine-resistant strains of P. falciparum.

Note: Due to geographical resistance and cross-resistance, consult current CDC guidelines.

* See Uses in AHFS Essentials for additional information.

Use: Off-Label: Adult

Treatment of uncomplicated, chloroquine-resistant P. vivax malariaLevel of Evidence [G]

Based on the World Health Organization (WHO) Guidelines for the Treatment of Malaria and the Center for Disease Control and Prevention (CDC) Treatment of Malaria guidelines, mefloquine given for the treatment of uncomplicated, chloroquine-resistant P. vivax malaria is effective and recommended in the management of this condition.

Level of Evidence Definitions

Level of Evidence Scale

Clinical Practice Guidelines

Malaria:

CDC, “Guidelines for Treatment of Malaria in the United States,” Table - July 2013

CDC, “Health Information for National Travel, 2014 ” (The Yellow Book)

CDC, “Treatment of Malaria (Guidelines for Clinicians),” July 2013

WHO, “Guidelines for the Treatment of Malaria,” 2010

Opportunistic Infections:

CDC, Prevention and Treatment of Opportunistic Infections Guidelines, Children, September 4, 2009

DHHS, Guidelines for the Prevention and Treatment of Opportunistic Infections Among HIV-Exposed and HIV-Infected Children, November 2013

DHHS, Guidelines for the Prevention and Treatment of Opportunistic Infections in HIV-Infected Adults and Adolescents, October 2014 [Note: Information contained within this monograph is pending revision based on these more recent guidelines]

Administration: Oral

Administer with food and with at least 240 mL of water. When used for malaria prophylaxis, dose should be taken once weekly on the same day each week. If vomiting occurs within 30 minutes after the dose, an additional full dose should be given; if it occurs within 30 to 60 minutes after dose, an additional half-dose should be given. Tablets may be crushed and suspended in a small amount of water, milk, or another beverage for persons unable to swallow tablets.

Administration: Pediatric

Oral: Administer with food and an ample amount of water, at least 240 mL of water for adults. If vomiting occurs within 30 minutes after a dose, repeat dose. If vomiting occurs within 30 to 60 minutes after a dose, an additional half-dose should be administered. If vomiting recurs, monitor closely and consider alternative treatment. Administering mefloquine on a full stomach may minimize nausea and vomiting. For patients unable to swallow tablets or unable to tolerate its bitter taste, crush tablets and mix with a small amount of water, milk, applesauce, chocolate syrup, jelly, or food immediately before administration. Pulverized dose of mefloquine can be enclosed in a gelatin capsule to mask bitter taste. When used for malaria prophylaxis, dose should be taken once weekly on the same day each week.

Dietary Considerations

Take with food and with at least 240 mL of water.

Storage/Stability

Store at 20°C to 25°C (68°F to 77°F).

Medication Patient Education with HCAHPS Considerations

What is this drug used for?

• It is used to treat or prevent malaria.

Frequently reported side effects of this drug

• Headache

• Nausea

• Vomiting

• Abdominal pain

• Diarrhea

• Lack of appetite

• Loss of strength and energy

• Muscle pain

Other side effects of this drug: Talk with your doctor right away if you have any of these signs of:

• Liver problems like dark urine, fatigue, lack of appetite, nausea, abdominal pain, light-colored stools, vomiting, or yellow skin

• Aplastic anemia like fever, sore throat, mouth sores, infections, bruising, or purple skin splotches

• Severe dizziness

• Passing out

• Agitation

• Change in balance

• Noise or ringing in the ears

• Anxiety

• Paranoia

• Depression

• Seizures

• Confusion

• Mood changes

• Behavioral changes

• Hallucination

• Abnormal heartbeat

• Slow heartbeat

• Chest pain

• Fast heartbeat

• Vision changes

• Eye pain

• Severe eye irritation

• Trouble sleeping

• Thoughts of suicide

• Signs of a significant reaction like wheezing; chest tightness; fever; itching; bad cough; blue skin color; seizures; or swelling of face, lips, tongue, or throat.

Note: This is not a comprehensive list of all side effects. Talk to your doctor if you have questions.

Consumer Information Use and Disclaimer: This information should not be used to decide whether or not to take this medicine or any other medicine. Only the healthcare provider has the knowledge and training to decide which medicines are right for a specific patient. This information does not endorse any medicine as safe, effective, or approved for treating any patient or health condition. This is only a brief summary of general information about this medicine. It does NOT include all information about the possible uses, directions, warnings, precautions, interactions, adverse effects, or risks that may apply to this medicine. This information is not specific medical advice and does not replace information you receive from the healthcare provider. You must talk with the healthcare provider for complete information about the risks and benefits of using this medicine.

Medication Safety Issues

Sound-alike/look-alike issues:

International issues:

Medication Guide and/or Vaccine Information Statement (VIS)

An FDA-approved patient medication guide, which is available with the product information and at http://www.fda.gov/downloads/Drugs/DrugSafety/ucm088616.pdf, must be dispensed with this medication.

Contraindications

Hypersensitivity to mefloquine, related compounds (eg, quinine and quinidine), or any component of the formulation; prophylactic use in patients with a history of seizures or psychiatric disorder (including active or recent history of depression, generalized anxiety disorder, psychosis, schizophrenia, or other major psychiatric disorders)

Documentation of allergenic cross-reactivity for quinine derivatives is limited. However, because of similarities in chemical structure and/or pharmacologic actions, the possibility of cross-sensitivity cannot be ruled out with certainty.

Warnings/Precautions

Concerns related to adverse effects:

• Agranulocytosis/aplastic anemia: Agranulocytosis and aplastic anemia have been reported.

• Altered cardiac conduction: Mefloquine may cause alterations in the ECG including sinus bradycardia, sinus arrhythmia, first-degree AV block, QT-interval prolongation, and abnormal T waves. Use caution or avoid concomitant use of agents known to cause QT-interval prolongation (eg, halofantrine, quinine, quinidine).

• Hypersensitivity reactions: Hypersensitivity reactions have occurred.

• Neuropsychiatric effects: [US Boxed Warning]: May cause neuropsychiatric adverse effects that can persist after mefloquine has been discontinued. During prophylactic use, if symptoms occur, discontinue therapy and substitute an alternative medication. Symptoms may develop early in the course of therapy. Due to the difficulty in identifying these symptoms in infants and children, monitor closely especially in pediatric patients. Psychiatric symptoms may include anxiety, paranoia, depression, hallucinations, and psychosis. Suicidal ideation and suicide have also been reported. Neurologic symptoms of dizziness or vertigo, tinnitus, and loss of balance may also occur and have been reported to be permanent in some cases. During prophylactic use, the occurrence of psychiatric symptoms such as acute anxiety, depression, restlessness, or confusion may be a prodrome to more serious neuropsychiatric adverse reactions. Use caution in activities requiring alertness and fine motor coordination (eg, driving, piloting planes, operating machinery) with neurologic symptoms.

Disease-related concerns:

• Cardiovascular disease: Use with caution in patients with significant cardiac disease; ECG changes (eg, sinus bradycardia, sinus arrhythmia, first-degree AV block, QT-interval prolongation, abnormal T waves) have been reported.

• Hepatic impairment: Use with caution in patients with hepatic impairment; elimination may be prolonged.

• Neuropsychiatric disorders: [US Boxed Warning]: Do not prescribe for prophylaxis in patients with major psychiatric disorders including patients with active depression, a recent history of depression, generalized anxiety disorder, psychosis, schizophrenia; use is contraindicated in these patients. Use with caution in patients with a previous history of depression.

• Ocular effects: Eye disorders (including optic neuropathy and retinal disorders) have been reported during treatment. If visual symptoms develop during treatment, prompt ophthalmologic evaluation is warranted; discontinuation of therapy may be necessary.

• Plasmodium falciparum infections: Appropriate use: In cases of life-threatening, serious, or overwhelming malaria infections due to Plasmodium falciparum, patients should be treated with intravenous antimalarial drug. Mefloquine may be given orally to complete the course.

• Plasmodium vivax infections: Appropriate use: In cases of acute Plasmodium vivax infection treated with mefloquine, patients should subsequently be treated with an 8-aminoquinoline derivative (eg, primaquine) to avoid relapse.

• Seizure disorder: When using for treatment, use with caution in patients with a history of seizures; may increase risk of seizures. Prophylactic use is contraindicated in patients with seizure disorder.

Concurrent drug therapy issues:

• Drug-drug interactions: Potentially significant interactions may exist, requiring dose or frequency adjustment, additional monitoring, and/or selection of alternative therapy. Consult drug interactions database for more detailed information.

Special populations:

• Pediatric: Early vomiting leading to treatment failure in children has been reported in some studies; consider alternate therapy if a second dose is not tolerated.

Other warnings/precautions:

• Appropriate use: Not recommended for the treatment of malaria acquired in Southeast Asia due to drug resistance (CDC 2013b).

• Prolonged use: If mefloquine is to be used for a prolonged period, liver function tests, evaluations for neuropsychiatric effects, and ophthalmic examinations should be performed periodically.

* See Cautions in AHFS Essentials for additional information.

Pregnancy Risk Factor

B

Pregnancy Considerations

Mefloquine crosses the placenta; however, clinical experience with mefloquine has not shown an increased risk of adverse effects in pregnant women. Malaria infection in pregnant women may be more severe than in nonpregnant women and may increase the risk of adverse pregnancy outcomes. CDC treatment guidelines are available for the use of mefloquine in the treatment of malaria during pregnancy (CDC 2013b).

Nonpregnant women of childbearing potential are advised to use contraception and avoid pregnancy during mefloquine therapy and for 3 months thereafter.

Breast-Feeding Considerations

Mefloquine is present in breast milk in small quantities (~3% to 4% of a 250 mg dose). The manufacturer recommends that caution be exercised when administering mefloquine to breastfeeding women. Exposure to small amounts of mefloquine from breast milk is considered safe for infants (CDC 2014).

Briggs' Drugs in Pregnancy & Lactation

• Mefloquine

Adverse Reactions

>10%: Central nervous system: Abnormal dreams (14%; Tickell-Painter 2017), insomnia (13%; Tickell-Painter 2017)

1% to 10%: Gastrointestinal: Vomiting (3%)

<1%, postmarketing, and/or case reports: Abdominal pain, abnormal sensory symptoms, abnormal T waves on ECG, aggressive behavior, agitation, agranulocytosis, alopecia, anaphylaxis, anorexia, aplastic anemia, arthralgia, asthenia, ataxia, atrioventricular block, auditory impairment, bradycardia, burning sensation, cardiac arrhythmia, cardiac conduction disturbance (transient), chest pain, chills, confusion, decreased hematocrit, depression, diarrhea, dizziness, drowsiness, dyspepsia, dyspnea, ECG changes, edema, emotional disturbance, emotional lability, encephalopathy, equilibrium disturbance, erythema, erythema multiforme, extrasystoles, fatigue, fever, first degree atrioventricular block, flushing, hallucination, headache, hepatic disease, hepatic failure, hyperhidrosis, hypersensitivity reaction, hypertension, hypotension, increased serum transaminases, insomnia, leukocytosis, leukopenia, loose stools, malaise, memory impairment, muscle cramps, myalgia, myasthenia, nausea, pain, palpitations, panic attack, paranoia, paresthesia, pneumonitis (possibly allergic), polyneuropathy, prolonged Q-T interval on ECG, pruritus, psychotic reaction, restlessness, seizure, sensorimotor neuropathy, sinus arrhythmia, sinus bradycardia, skin rash, Stevens-Johnson syndrome, suicidal ideation (causal relationship not established), syncope, tachycardia, telogen effluvium, thrombocytopenia, tinnitus, tremor, urticaria, vertigo, vestibular disturbance, visual disturbance

* See Cautions in AHFS Essentials for additional information.

Allergy and Idiosyncratic Reactions

• QuiNIDine/QuiNINE Derivative Allergy

Metabolism/Transport Effects

Substrate of CYP3A4 (major); Note: Assignment of Major/Minor substrate status based on clinically relevant drug interaction potential

Drug Interactions Open Interactions

Aminoquinolines (Antimalarial): May enhance the adverse/toxic effect of Mefloquine. Specifically, the risk for QTc-prolongation and the risk for convulsions may be increased. Mefloquine may increase the serum concentration of Aminoquinolines (Antimalarial). Management: Avoid concurrent use, and delay administration of mefloquine until at least 12 hours after the last dose of an aminoquinoline antimalarial when possible. Risk X: Avoid combination

Amodiaquine: May enhance the adverse/toxic effect of Mefloquine. Specifically, the risk for vision problems may be increased. Risk C: Monitor therapy

Anticonvulsants: Mefloquine may diminish the therapeutic effect of Anticonvulsants. Mefloquine may decrease the serum concentration of Anticonvulsants. Management: Mefloquine is contraindicated for malaria prophylaxis in persons with a history of convulsions. Monitor anticonvulsant concentrations and treatment response closely with concurrent use. Risk D: Consider therapy modification

Antipsychotic Agents (Phenothiazines): Antimalarial Agents may increase the serum concentration of Antipsychotic Agents (Phenothiazines). Risk C: Monitor therapy

Aprepitant: May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors). Risk C: Monitor therapy

Artemether: May enhance the adverse/toxic effect of Antimalarial Agents. Management: Artemether/Lumefantrine (combination product) should not be used with other antimalarials unless there is no other treatment option. Risk X: Avoid combination

Bosentan: May decrease the serum concentration of CYP3A4 Substrates (High risk with Inducers). Risk C: Monitor therapy

Celiprolol: Mefloquine may enhance the bradycardic effect of Celiprolol. Risk C: Monitor therapy

Clofazimine: May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors). Risk C: Monitor therapy

Conivaptan: May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors). Risk X: Avoid combination

CYP3A4 Inducers (Moderate): May decrease the serum concentration of CYP3A4 Substrates (High risk with Inducers). Risk C: Monitor therapy

CYP3A4 Inducers (Strong): May increase the metabolism of CYP3A4 Substrates (High risk with Inducers). Management: Consider an alternative for one of the interacting drugs. Some combinations may be specifically contraindicated. Consult appropriate manufacturer labeling. Risk D: Consider therapy modification

CYP3A4 Inhibitors (Moderate): May decrease the metabolism of CYP3A4 Substrates (High risk with Inhibitors). Risk C: Monitor therapy

CYP3A4 Inhibitors (Strong): May decrease the metabolism of CYP3A4 Substrates (High risk with Inhibitors). Risk D: Consider therapy modification

Dabrafenib: May decrease the serum concentration of CYP3A4 Substrates (High risk with Inducers). Management: Seek alternatives to the CYP3A4 substrate when possible. If concomitant therapy cannot be avoided, monitor clinical effects of the substrate closely (particularly therapeutic effects). Risk D: Consider therapy modification

Dapsone (Systemic): Antimalarial Agents may enhance the adverse/toxic effect of Dapsone (Systemic). Specifically, concomitant use of antimalarial agents with dapsone may increase the risk of hemolytic reactions. Dapsone (Systemic) may enhance the adverse/toxic effect of Antimalarial Agents. Specifically, concomitant use of dapsone with antimalarial agents may increase the risk for hemolytic reactions. Management: Closely monitor patients for signs/symptoms of hemolytic reactions with concomitant use of dapsone and antimalarial agents, particularly in patients deficient in glucose-6-phosphate dehydrogenase (G6PD), methemoglobin reductase, or with hemoglobin M. Risk D: Consider therapy modification

Dapsone (Topical): Antimalarial Agents may enhance the adverse/toxic effect of Dapsone (Topical). Specifically, the risk of hemolytic reactions may be increased. Management: Closely monitor for signs/symptoms of hemolytic reactions with concomitant use of topical dapsone and antimalarial agents. Patients with glucose-6-phosphate dehydrogenase deficiency may be at particularly high risk for adverse hematologic effects. Risk D: Consider therapy modification

Deferasirox: May decrease the serum concentration of CYP3A4 Substrates (High risk with Inducers). Risk C: Monitor therapy

Duvelisib: May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors). Risk C: Monitor therapy

Enzalutamide: May decrease the serum concentration of CYP3A4 Substrates (High risk with Inducers). Management: Concurrent use of enzalutamide with CYP3A4 substrates that have a narrow therapeutic index should be avoided. Use of enzalutamide and any other CYP3A4 substrate should be performed with caution and close monitoring. Risk D: Consider therapy modification

Erdafitinib: May decrease the serum concentration of CYP3A4 Substrates (High risk with Inducers). Risk C: Monitor therapy

Erdafitinib: May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors). Risk C: Monitor therapy

Fosaprepitant: May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors). Risk C: Monitor therapy

Fosnetupitant: May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors). Risk C: Monitor therapy

Fusidic Acid (Systemic): May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors). Risk X: Avoid combination

Halofantrine: Mefloquine may enhance the QTc-prolonging effect of Halofantrine. Risk X: Avoid combination

Haloperidol: QT-prolonging Agents (Indeterminate Risk - Caution) may enhance the QTc-prolonging effect of Haloperidol. Risk C: Monitor therapy

Idelalisib: May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors). Risk X: Avoid combination

Ivosidenib: May decrease the serum concentration of CYP3A4 Substrates (High risk with Inducers). Risk C: Monitor therapy

Larotrectinib: May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors). Risk C: Monitor therapy

Lumefantrine: Antimalarial Agents may enhance the adverse/toxic effect of Lumefantrine. Management: Artemether/Lumefantrine (combination product) should not be used with other antimalarials unless there is no other treatment option. Risk X: Avoid combination

MiFEPRIStone: May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors). Management: Minimize doses of CYP3A4 substrates, and monitor for increased concentrations/toxicity, during and 2 weeks following treatment with mifepristone. Avoid cyclosporine, dihydroergotamine, ergotamine, fentanyl, pimozide, quinidine, sirolimus, and tacrolimus. Risk D: Consider therapy modification

Mitotane: May decrease the serum concentration of CYP3A4 Substrates (High risk with Inducers). Management: Doses of CYP3A4 substrates may need to be adjusted substantially when used in patients being treated with mitotane. Risk D: Consider therapy modification

Netupitant: May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors). Risk C: Monitor therapy

Palbociclib: May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors). Risk C: Monitor therapy

QT-prolonging Agents (Highest Risk): QT-prolonging Agents (Indeterminate Risk - Caution) may enhance the QTc-prolonging effect of QT-prolonging Agents (Highest Risk). Management: Monitor for QTc interval prolongation and ventricular arrhythmias when these agents are combined. Patients with additional risk factors for QTc prolongation may be at even higher risk. Risk C: Monitor therapy

QuiNIDine: May enhance the adverse/toxic effect of Mefloquine. Specifically, the risk for QTc-prolongation and the risk for convulsions may be increased. Management: Avoid concurrent use, and delay administration of mefloquine until at least 12 hours after the last dose of quinidine when possible. Risk X: Avoid combination

QuiNINE: May enhance the adverse/toxic effect of Mefloquine. Specifically, the risk for QTc-prolongation and the risk for convulsions may be increased. Mefloquine may increase the serum concentration of QuiNINE. Management: Avoid concurrent use, and delay administration of mefloquine until at least 12 hours after the last dose of quinine when possible. Risk X: Avoid combination

Sarilumab: May decrease the serum concentration of CYP3A4 Substrates (High risk with Inducers). Risk C: Monitor therapy

Siltuximab: May decrease the serum concentration of CYP3A4 Substrates (High risk with Inducers). Risk C: Monitor therapy

Simeprevir: May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors). Risk C: Monitor therapy

Stiripentol: May increase the serum concentration of CYP3A4 Substrates (High risk with Inhibitors). Management: Use of stiripentol with CYP3A4 substrates that are considered to have a narrow therapeutic index should be avoided due to the increased risk for adverse effects and toxicity. Any CYP3A4 substrate used with stiripentol requires closer monitoring. Risk D: Consider therapy modification

Tocilizumab: May decrease the serum concentration of CYP3A4 Substrates (High risk with Inducers). Risk C: Monitor therapy

Food Interactions

Food increases bioavailability by ~40%. Management: Take with food and at least 8 ounces of water. Maintain adequate nutrition and hydration, unless instructed to restrict fluid intake.

Genes of Interest

• Cytochrome P450 3A4
• P-Glycoprotein

Monitoring Parameters

When use is prolonged, periodic liver function tests, evaluations for neuropsychiatric effects, and ocular examinations

Advanced Practitioners Physical Assessment/Monitoring

Obtain periodic liver function tests with prolonged therapy. Have patient obtain regular ocular exams. Assess patient closely for any development of psychiatric symptoms; may persist long after mefloquine has been discontinued.

Nursing Physical Assessment/Monitoring

Check ordered labs and report abnormalities. Monitor patient closely for any development of psychiatric symptoms (anxiety, paranoia, depression, hallucinations, and psychosis); may persist long after mefloquine has been discontinued. Advise patient about the importance of carrying medication guide and wallet card provided when mefloquine is dispensed for malaria. Teach patient importance of adequate hydration.

Dosage Forms: US

Excipient information presented when available (limited, particularly for generics); consult specific product labeling.

Tablet, Oral, as hydrochloride:

Generic: 250 mg

Dosage Forms: Canada

Excipient information presented when available (limited, particularly for generics); consult specific product labeling.

Tablet, Oral, as hydrochloride:

Generic: 250 mg

Anatomic Therapeutic Chemical (ATC) Classification

• P01BC02

Generic Available (US)

Yes

Pricing: US

Tablets (Mefloquine HCl Oral)

250 mg (per each): $10.59

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Mechanism of Action

Mefloquine is a quinoline-methanol compound structurally similar to quinine; mefloquine's effectiveness in the treatment and prophylaxis of malaria is due to the destruction of the asexual blood forms of the malarial pathogens that affect humans, Plasmodium falciparum, P. vivax

Pharmacodynamics/Kinetics

Absorption: Well absorbed; interpatient variability with rate observed (WHO, 2010); more complete absorption when administered as a suspension compared with tablets

Distribution: Distributes into tissues, erythrocytes, blood, urine, CSF

V_d: Children 4 to 10 years: Mean: ~18 to 19 L/kg (Price 1999); Adults: ~20 L/kg

Protein binding: ~98%

Metabolism: Extensively hepatic primarily by CYP3A4 to 2,8-bis-trifluoromethyl-4-quinoline carboxylic acid (inactive) and other metabolites

Bioavailability: Increased by food

Half-life elimination: Children 4 to 10 years: Mean range: 11.6 to 13.6 days (range: 6.5 to 33 days) (Price 1999); Adults: ~3 weeks (range: 2 to 4 weeks); may be decreased during infection (2 weeks) (WHO 2010)

Time to peak, plasma: ~17 hours (range: 6 to 24 hours)

Excretion: Primarily bile and feces; urine (9% of total dose as unchanged drug, 4% of total dose as primary metabolite)

Local Anesthetic/Vasoconstrictor Precautions

No information available to require special precautions

Effects on Dental Treatment

No significant effects or complications reported

Effects on Bleeding

No information available to require special precautions

Index Terms

Lariam; Mefloquine Hydrochloride

FDA Approval Date

May 02, 1989

References

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Brand Names: International

Eloquine (ET, TR); Lariam (AE, AT, AU, BE, BF, BG, BH, BJ, CH, CI, CL, CY, CZ, DE, DK, ET, FI, FR, GB, GH, GM, GN, GR, HK, HN, HU, IQ, IR, IT, JO, KE, KR, KW, LB, LR, LU, LY, MA, ML, MR, MT, MU, MW, NE, NG, NL, NO, OM, PE, PH, PL, PT, QA, RU, SA, SC, SD, SE, SI, SK, SL, SN, SY, TN, TR, TZ, UA, UG, UY, VN, YE, ZA, ZM, ZW); Laricam (JP); Larimef (BD, IN); Malariquin (EG); Malarium (BD); Malarivent T (EG); Mefliam (ZA); Meflon (BD); Melophar (AE); Mephaquin (BB, BM, BS, BZ, CH, EC, GY, JM, PE, PT, SG, SR, TT, VN); Mequin (TH); Suton (TW); Tropicur (AR); Vexam (BD)

Last Updated 2/20/20