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What is Arakoda, and how does it work?
What are the side effects of Arakoda?
Arakoda may cause serious side effects, including:
- Allergic (hypersensitivity) reactions. Allergic reactions can happen after you take Arakoda. Signs and symptoms of an allergic reaction may not happen right away (delayed reaction). Get medical help right away if you have any signs or symptoms of an allergic reaction including:
The most common side effects of Arakoda include:
- back pain,
- increased liver enzyme levels in your blood,
- motion sickness,
- abnormal dreams and
Other side effects of Arakoda include eye problems. Some people who take Arakoda can have a problem with the cornea of the eye called vortex keratopathy. This problem can be seen during an eye exam. Vortex keratopathy does not cause vision problems and will usually go away after you stop taking Arakoda.
These are not all the possible side effects of Arakoda.
Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA- 1088.
What is the dosage for Arakoda?
Tests To Be Performed Prior To Arakoda Dose Initiation
- All patients must be tested for glucose-6-phosphate dehydrogenase (G6PD) deficiency prior to prescribing Arakoda.
- Pregnancy testing is recommended for females of reproductive potential prior to initiating treatment with Arakoda.
Recommended Dosage And Administration Instructions
The recommended dosage of Arakoda is described in Table 1 below. Arakoda can be administered for up to 6 months of continuous dosing.
Table 1: Recommended Dosage of Arakoda in Patients (18 Years of Age and Older)
|Loading regimen||For each of the 3 days before travel to a malarious area||200 mg (2 of the 100 mg tablets) once daily for 3 days|
|Maintenance regimen||While in the malarious area||200 mg (2 of the 100 mg tablets) once weekly - start 7 days after the last loading regimen dose|
|Terminal prophylaxis regimen||In the week following exit from the malarious area||200 mg (2 of the 100 mg tablets) taken one time, 7 days after the last maintenance dose|
- Administer Arakoda with food.
- Swallow the tablet whole. Do not break, crush or chew the tablets.
- Complete the full course of Arakoda including the loading dose and the terminal dose.
Table 2: How to Replace Missed Doses of Arakoda
|Dose(s) Missed||How to Replace Missed Dose(s):|
|1 Loading dose||1 dose of 200 mg (2 of the 100 mg tablets) so that a total of 3 daily loading doses have been taken. Begin maintenance dose 1 week after the last loading dose.|
|2 Loading doses||2 doses of 200 mg (2 of the 100 mg tablets) on 2 consecutive days so that a total of 3 daily loading doses have been taken. Begin maintenance dose 1 week after the last loading dose.|
|1 Maintenance (weekly) dose||1 dose of 200 mg (2 of the 100 mg tablets) on any day up to the time of the next scheduled weekly dose.|
|2 Maintenance (weekly) doses||1 dose of 200 mg (2 of the 100 mg tablets) on any day up to the time of the next scheduled weekly dose.|
|3 or more Maintenance (weekly) doses||2 doses of 200 mg (2 of the 100 mg tablets), taken as 200 mg (2 of the 100 mg tablets) once daily for 2 days up to the time of the next weekly dose.|
|Terminal prophylaxis dose||1 dose of 200 mg (2 of the 100 mg tablets) as soon as remembered.|
What drugs interact with Arakoda?
Effect Of Arakoda On Organic Cation Transporter-2 (OCT2) And Multidrug And Toxin Extrusion (MATE) Substrates
- The effect of coadministration of tafenoquine on the pharmacokinetics of OCT2 and MATE substrates in humans is unknown.
- However, in vitro observations suggest the potential for increased concentrations of these substrates which may increase the risk of toxicity of these drugs.
- Avoid coadministration of Arakoda with OCT2 and MATE substrates (e.g., dofetilide, metformin).
- If coadministration cannot be avoided, monitor for drug-related toxicities and consider dosage reduction if needed based on approved product labeling of the coadministered drug.
Is Arakoda safe to use while pregnant or breastfeeding?
- There is a potential risk of Arakoda to a fetus. Women should inform their healthcare provider of a known or suspected pregnancy.
- Females should use effective contraception during treatment with Arakoda and for 3 months after the final dose.
- Women with a G6PD-deficient infant, or if they do not know the G6PD status of their infant, not to breastfeed during treatment with Arakoda and for 3 months after the final dose
Latest Medications News
Daily Health News
Arakoda is a prescription medicine used to help prevent malaria in people 18 years of age and older. Malaria is a serious disease of the blood that is spread by infected mosquitos. It is not known if Arakoda is safe and effective in children. Serious side effects of Arakoda include allergic (hypersensitivity) reactions.
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Report Problems to the Food and Drug Administration
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.