E Aps
E Aps Uses, Dosage, Side Effects, Food Interaction and all others data.
E Aps is a potent and rapidly-acting blood schizontocide derived from the leaves of the chinese herb, Armesia annua. The exact mode of action is not clear but clinical studies have confirmed the effectiveness of artesunate in P. vivax and falciparum malaria.
E Aps is an artemisinin derivative that is metabolized to DHA, which generates free radicals to inhibit normal function of Plasmodium parasites. It has a short duration of action due to its short half life, and a moderate therapeutic index. Patients should be counselled regarding the risk of post treatment hemolytic anemia and hypersenstivity.
| Trade Name | E Aps |
| Availability | Prescription only |
| Generic | Artesunate |
| Artesunate Other Names | Artesunate, Artesunato, Artesunatum, Artesunic acid |
| Related Drugs | doxycycline, clindamycin, hydroxychloroquine, Plaquenil, Cleocin |
| Type | Vial |
| Formula | C19H28O8 |
| Weight | Average: 384.425 Monoisotopic: 384.178417862 |
| Protein binding | Artesunate and its metabolite DHA are approximately 93% protein bound in plasma. Artesunate can bind to serum albumin. |
| Groups | Approved, Investigational |
| Therapeutic Class | Anti-malarial drugs |
| Manufacturer | Veritaz Healthcare Ltd |
| Available Country | India |
| Last Updated: | September 19, 2023 at 7:00 am |
Uses
E Aps can quickly and reliably control the acute attack of malaria. It is suitable to salvage the patients with pernicious malaria and treat P. falciparum malaria and P. vivax malaria. It is effective against malaria caused by chloroquine resistant strain of plasmodium falciparum.
E Aps is also used to associated treatment for these conditions: Acute Uncomplicated Plasmodium Falciparum Malaria, Malaria, Cerebral, Severe Malaria
How E Aps works
E Aps is metabolized to the active DHA. the endoperoxide bridge of DHA reacts with heme, generating free radicals which inhibit protein and nucleic acid synthesis of the Plasmodium parasites during all erythrocytic stages. Reactions with these free radicals can also lead to alkylation of parasitic proteins such as a calcium adenosine triphosphatase and EXP1, a glutathione S-transferase.
Dosage
E Aps dosage
Adult: 5 days treatment: on the 1st day 2 tablets twice and 2nd day onward 1 tablet twice daily for remaining 4 days
Children:
- 1-3 years: 5 days treatment: on the 1st day ½ tablet twice and 2nd day onward ¼ tablet twice daily for remaining 4 days
- 4-5 years: 5 days treatment: on the 1st day 1 tablet twice and 2nd day onward ½ tablet twice daily for remaining 4 days
- 6-12 years: 5 days treatment: on the 1st day ½ tablet twice, 2nd day 1 tablet twice and 3rd day onward ½ tablet twice daily for remaining 3 days
Prophylmcis: 100 mg tablet once a week, from 1 week before entering malarial areas, to 4 weeks after leaving the area.
Side Effects
Transient and reversible reticulocytopaenia, drug fever, rash, bradycardia, transient 1st-degree heart block and reversible elevation of serum transaminases.
Toxicity
Data regarding overdoses of artesunate are rare. Patients experiencing an overdose may present with pancytopenia, melena, seizures, multiorgan failure, and death. Treat overdose with symptomatic and supportive measures.
Precaution
Hepatic or renal insufficiency; Pregnancy and lactation.
Interaction
Antimalarial potentiating action seen with mefloquine, primaquine and tetracycline. Additive effect with chloroquine. Antagonistic effect with pyrimethamine and sulphonamides.
Food Interaction
No interactions found.E Aps Drug Interaction
Unknown: acetylcysteine, amphetamine / dextroamphetamine, amphetamine / dextroamphetamine, epinephrine, aspirin, celecoxib, ubiquinone, ubiquinone, glutamic acid, lysine, acetaminophen, fluoxetine, bioflavonoids, thiamine, cyanocobalamin, ascorbic acid, cholecalciferol, menaquinone, zinc sulfate, ondansetron
Volume of Distribution
The volume of distribution of artesunate is 68.5L while the volume of distribution of DHA is 59.7L.
Elimination Route
The Cmax of artesunate is 3.3µg/mL while the Cmax of the active metabolite DHA is 3.1µg/mL. The AUC of artesunate is 0.7µg*h/mL while the AUC of DHA is 3.5µg*h/mL. After intravenous artesunate, DHA has a Tmax of 0.5-15 minutes in adult patients and 21-64 minutes in pediatric patients. Intramuscular artesunate has a Tmax of 8-12 minutes. Infants less than 6 months old will have a higher AUC due to an undeveloped UGT metabolic pathway.
Half Life
The elimination half life of artesunate is 0.3h with a range of 0.1-1.8h. The elimination half life of DHA is 1.3h with a range of 0.9-2.9h. Half life after intramuscular administration is 48 min in children and 41 min in adults.
Clearance
The clearance of artesunate is 180L/h while the clearance of DHA is 32.3L/h.
Elimination Route
The main route of elimination in humans is unknown. In rats, a dose of artesunate is 56.1% eliminated in the urine and 38.5% in the feces.
Pregnancy & Breastfeeding use
Pregnancy category is not classified. FDA has yet not classified the drug into a specific pregnancy catagory.
Contraindication
Hypersensitivity.
Innovators Monograph
You find simplified version here E Aps
E Aps contains Artesunate see full prescribing information from innovator E Aps Monograph, E Aps MSDS, E Aps FDA label
FAQ
What is E Aps used for?
E Aps is a medication used to treat malaria. The intravenous form is preferred to quinine for severe malaria. Often it is used as part of combination therapy, such as artesunate plus mefloquine.
How safe is E Aps?
Intravenous E Aps was safe and effective in treating severe malaria in adults in the United States, researchers reported in Clinical Infectious Diseases.
What are the common side effects of E Aps?
Common side effects of E Aps are include:
- Hives.
- Rash.
- Hemoglobinuria.
- Seizures.
- Neuropsychiatric reactions.
- Reversible neurologic changes.
Is E Aps safe during pregnancy?
E Aps and other antimalarials also appear to be effective and safe in the first trimester of pregnancy, when development of malaria carries a high risk of miscarriage.
Is E Aps safe during breastfeeding?
Limited information indicates that a maternal dose of 200 mg orally produced low levels in milk and would not be expected to cause any adverse effects in breastfed infants, especially if the infant is older than 2 months.
Can I drink alcohol with E Aps?
E Aps and alcohol together has not been proven to cause harm, therefore it is safe to drink while taking your malaria tablets. However, as always, it is best to consume alcohol within the recommended guidelines to stay safe and look after your health.
Can I drive after taking E Aps?
E Aps causes drowsiness and dizziness it is advisable to you do not drive unless you are alert.
When should be taken of E Aps?
It should be taken between 8 and 12 hours after the last injection of E Aps. Until the patient is able to take oral medication.
How should I take E Aps?
The recommended dosage of E Aps for Injection is 2.4 mg/kg administered intravenously at 0 hours, 12 hours, and 24 hours, and thereafter, administered once daily until the patient is able to tolerate oral antimalarial therapy.
How long does E Aps take to work?
E Aps are active against the different asexual forms of the Plasmodium parasites and clear parasitemia within 48 to 72 hours.
What is the half life of E Aps?
The elimination half-life of E Aps is about 0.22 hours.
How often can I take E Aps?
The adult dose is 1 tablet weekly. Child dosage is also once a week, but the amount will depend on their weight. It should be started 3 weeks before you travel and taken all the time you're in a risk area, and for 4 weeks after you get back.
How long can I take E Aps?
Continue E Aps treatment one dose a day for a maximum of 7 days.
Who should not take E Aps?
You should not use E Aps if you are allergic to it. Tell your doctor if you have ever had kidney problems. Tell your doctor if you are pregnant. Malaria is more likely to cause serious illness or death in a pregnant woman.
What happen if I overdose on E Aps?
The overdose was associated with pancytopenia, melena, seizures, multiorgan failure and death. Treatment of overdose should consist of general supportive measures.
What happens if I miss a dose?
In a medical setting you are not likely to miss a dose.
Does E Aps cause hypoglycemia?
The present study suggests that E Aps could cause duration-dependent hemolysis and hypoglycemia probably via free radical generation, inactivation of antioxidant enzymes, and stimulation of insulin secretion.
Can E Aps affects my heart ?
Study showed that intravenous E Aps does not have significant cardiovascular effects.
Can E Aps affect my kidneys?
These findings suggest that E Aps decreases glomerular filtration rate and increases renal blood flow and urinary excretion of Na, Cl, and K.
Can E Aps affects my liver?
E Aps administration of high doses of E Aps by the oral route produced considerable damage to the liver.
Will E Aps affect my fertility?
E Aps did not cause any significant effects in short-term administration but significantly reduced the aforesaid parameters in long-term administration. There were visible lesions in the testicular and epididymal histological studies, although fertility was not significantly reduced.
