Anidulafungin is an antifungal medication used to treat certain types of fungal infections, such as esophageal candidiasis (EC) (a fungal infection of the esophagus), candidemia (when the bloodstream is infected with Candida yeast), and other serious fungal infections of the body. It is a semisynthetic echinocandin, derived from a fermentation product of Glarea lozoyensis. Anidulafungin is sold under the brand name Eraxis and is available in powder and intravenous forms.
Anidulafungin is used to treat certain fungal infections, including:
| Brand Name | Anidulafungin |
|---|---|
| Type | |
| Weight | |
| Generic | Anidulafungin |
| Manufacturer | |
| Available in | English বাংলা |
Anidulafungin works by disrupting cell wall formation of the fungus, inhibiting the ability of the fungus to produce essential components necessary for its growth. This causes the fungus to die off, stopping the spread of the infection. Anidulafungin is considered non-cytotoxic, meaning it does not cause damage to human cells.
It may take several days for symptoms to improve, however, some users have reported feeling relief within 24 hours. The length of time it takes for Anidulafungin to work may vary based on the type and severity of the infection.
Anidulafungin is poorly absorbed when taken orally. Intravenous administration is the preferred route of administration.
Anidulafungin is eliminated primarily in the feces. It is also eliminated in small amounts in the urine.
| Adults | Pediatric (1 Month of Age and Older) |
| Candidemia and other forms of Candida infections | |
| 200 mg loading dose on Day 1, followed by 100 mg once daily maintenance dose thereafter for at least 14 days after the last positive culture | 3 mg/kg (not to exceed 200 mg) loading dose on Day 1, followed by 1.5 mg/kg (not to exceed 100 mg) once daily maintenance dose thereafter for at least 14 days after the last positive culture |
| Esophageal Candidiasis | |
| 100 mg loading dose on Day 1, followed by 50 mg once daily maintenance dose thereafter for a minimum of 14 days and for at least 7 days following resolution of symptoms | Not approved |
The recommended dose of Anidulafungin is 200 mg administered intravenously on the first day, followed by 100 mg administered intravenously once daily. The duration of treatment depends on the type and severity of the infection being treated.
Anidulafungin should be administered intravenously. It should not be administered orally as it is poorly absorbed.
The most common side effects associated with Anidulafungin include:
The most significant toxicity associated with Anidulafungin is kidney failure. Other rare but serious side effects can include liver failure, convulsions, and coma.
Before taking Anidulafungin , tell your healthcare provider if you have any allergies, including to other antifungal medications, such as caspofungin or micafungin. Also, tell your healthcare provider if you are taking any other medications, including over-the-counter medications, supplements, or vitamins. Talk to your healthcare provider about any other medical conditions you have before taking Anidulafungin .
Anidulafungin may interact with a variety of medications. Therefore, it is important to inform your healthcare provider of all medications you are taking. Some of the drug interactions with Anidulafungin include:
Anidulafungin may interact with certain diseases, such as kidney problems, liver problems, or other serious infections. Tell your healthcare provider if you have any of these conditions or if you have had them in the past.
Anidulafungin may interact with other drugs, including certain antibiotics, antipsychotics, beta blockers, and oral corticosteroids. It is important to tell your healthcare provider about all medications you are taking. Some drug interactions with Anidulafungin can be serious and may require dose adjustment or discontinuation of the medication.
Anidulafungin is not known to interact with any food or beverages. However, it is always best to talk to your healthcare provider about any dietary restrictions while taking Anidulafungin .
Anidulafungin should not be used during pregnancy. There is limited data available on the safety of Anidulafungin for pregnant woman and no well-controlled studies have been done in pregnant women.
It is not known whether Anidulafungin is secreted in human milk. Due to the potential for serious adverse reactions in nursing infants, Anidulafungin should not be used in nursing mothers unless the potential benefits outweigh the potential risks.
If an overdose of Anidulafungin occurs, promptly seek medical attention. Symptoms of an overdose may include nausea, vomiting, diarrhea, and abdominal pain.
Anidulafungin should not be used in patients who are hypersensitive to it or any of its components. It should also not be used in patients with known or suspected heart valve infection (endocarditis).
The recommended dose of Anidulafungin is 200 mg administered intravenously on the first day, followed by 100 mg administered intravenously once daily. The duration of treatment depends on the type and severity of the infection being treated.
Anidulafungin should be stored at room temperature away from moisture and heat. Do not freeze.
The volume of distribution for Anidulafungin is 3.3 L.
The half-life of Anidulafungin is approximately 52 hours.
The clearance of Anidulafungin is approximately 64 mL/min.
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