What is Koxylar?
Koxylar is used to treat tuberculosis (TB). It is used with other medicines for TB. Koxylar may also be used for other problems as determined by your doctor.
To help clear up your tuberculosis (TB) infection completely, you must keep taking Koxylar for the full time of treatment, even if you begin to feel better. This is very important. It is also important that you do not miss any doses.
Koxylar is available only with your doctor's prescription.
Once a medicine has been approved for marketing for a certain use, experience may show that it is also useful for other medical problems. Although this use is not included in product labeling, Koxylar is used in certain patients with the following medical condition:
- Atypical mycobacterial infections, such as Mycobacterium avium complex (MAC)
Koxylar indications
Koxylar hydrochloride is indicated for the treatment of pulmonary tuberculosis. It should not be used as the sole antituberculous drug, but should be used in conjunction with at least one other antituberculous drug. Selection of the companion drug should be based on clinical experience, considerations of comparative safety and appropriate in-vitro susceptibility studies. In patients who have not received previous antituberculous therapy, i.e., initial treatment, the most frequently used regimens have been the following:
- Koxylar plus isoniazid
- Koxylar plus isoniazid plus streptomycin.
In patients who have received previous antituberculous therapy, mycobacterial resistance to other drugs used in initial therapy is frequent. Consequently, in such retreatment patients, Koxylar should be combined with at least one of the second line drugs not previously administered to the patient and to which bacterial susceptibility has been indicated by appropriate in-vitro studies. Antituberculous drugs used with Koxylar have included cycloserine, ethionamide, pyrazinamide, viomycin and other drugs. Isoniazid, aminosalicylic acid, and streptomycin have also been used in multiple drug regimens. Alternating drug regimens have also been utilized.
How should I use Koxylar?
Use Koxylar as directed by your doctor. Check the label on the medicine for exact dosing instructions.
- Take Koxylar by mouth with or without food at the same time each day.
- Do not take an antacid that has aluminum hydroxide in it within 4 hours after you take Koxylar.
- If you miss a dose of Koxylar, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.
Ask your health care provider any questions you may have about how to use Koxylar.
Uses of Koxylar in details
Use: Labeled Indications
Treatment of pulmonary tuberculosis in conjunction with other antituberculosis agents
Off Label Uses
Mycobacterium avium complex disease
Based on the Department of Health and Human Services (HHS) Guidelines for the Prevention and Treatment of Opportunistic Infections in HIV-Infected Adults and Adolescents, Koxylar, in combination with other appropriate antimycobacterial drugs, is effective and recommended for the treatment and chronic maintenance therapy (secondary prophylaxis) of disseminated MAC disease in HIV-infected patients.
Based on the American Thoracic Society (ATS) and Infectious Diseases Society of America (IDSA) Guideline for the Diagnosis, Treatment, and Prevention of Nontuberculosis Mycobacterial Disease, Koxylar, in combination with other appropriate antimycobacterial drugs, is effective and recommended for the treatment of MAC pulmonary and/or disseminated disease.
Nontuberculous mycobacterial disease (M. kansasii)
Data from a small prospective, single-arm study and a larger retrospective study support the use of Koxylar, in combination with clarithromycin and rifampin, in the treatment of susceptible Mycobacterium kansasii pulmonary disease. Additional trials may be necessary to further define the role of Koxylar in this condition.
Based on the ATS/IDSA Guideline for the Diagnosis, Treatment, and Prevention of Nontuberculous Mycobacterial Diseases Koxylar, in combination with rifampin and isoniazid, is effective and recommended for the treatment of susceptible M. kansasii pulmonary disease
Tuberculous meningitis (drug-susceptible)
Based on the American Thoracic Society (ATS)/Centers for Disease Control and Prevention (CDC)/Infectious Disease Society of America (IDSA) Treatment of Drug-Susceptible Tuberculosis guidelines, Koxylar, in combination with other antitubercular drugs, is effective and recommended for initial treatment of tuberculous meningitis.
Koxylar description
An antitubercular agent that inhibits the transfer of mycolic acids into the cell wall of the tubercle bacillus. It may also inhibit the synthesis of spermidine in mycobacteria. The action is usually bactericidal, and the drug can penetrate human cell membranes to exert its lethal effect. (From Smith and Reynard, Textbook of Pharmacology, 1992, p863)
Koxylar dosage
Koxylar Dosage
Applies to the following strength(s): 100 mg; 400 mg
The information at Drugs.com is not a substitute for medical advice. Always consult your doctor or pharmacist.
Usual Adult Dose for:
- Tuberculosis - Active
- Mycobacterium avium-intracellulare - Treatment
- Mycobacterium avium-intracellulare - Prophylaxis
Usual Pediatric Dose for:
- Tuberculosis - Active
- Mycobacterium avium-intracellulare - Treatment
- Mycobacterium avium-intracellulare - Prophylaxis
Additional dosage information:
- Renal Dose Adjustments
- Liver Dose Adjustments
- Dose Adjustments
- Precautions
- Dialysis
- Other Comments
Usual Adult Dose for Tuberculosis - Active
Initial treatment: 15 mg/kg orally once a day for 6 to 8 weeks with concurrent isoniazid therapy.
Retreatment: 25 mg/kg orally once a day for 60 days concurrently with at least one other anti-TB drug. After 60 days, decrease dose to 15 mg/kg orally once a day.
As an alternative to single daily dose, a dose of 40 mg/kg orally twice a week or 30 mg/kg orally 3 times a week can be administered. This generally follows 2 weeks of daily therapy. This regimen allows directly observed therapy (DOT).
Usual Adult Dose for Mycobacterium avium-intracellulare - Treatment
900 mg orally once a day. Pulmonary AVI treatment consists of clarithromycin and 2 to 4 other drugs such as Koxylar, rifampin, clofazimine, and/or other agents. The duration of treatment is 18 to 24 months.
Disseminated MAI treatment consists of clarithromycin or azithromycin and 1 to 3 other drugs such as Koxylar, clofazamine, ciprofloxacin, ofloxacin, rifampin, rifabutin, or amikacin. As long as clinical and microbiological response is documented, therapy should be continued for life.
Usual Adult Dose for Mycobacterium avium-intracellulare - Prophylaxis
15 mg/kg orally once a day. Used in combination therapy with clarithromycin or azithromycin. Therapy should be continued for life.
Usual Pediatric Dose for Tuberculosis - Active
Greater than 13 years:
Initial treatment: 15 mg/kg orally once a day for 6 to 8 weeks with concurrent isoniazid therapy.
Retreatment: 25 mg/kg orally once a day for 60 days concurrently with at least one other anti-TB drug. After 60 days, decrease dose to 15 mg/kg orally once a day.
As an alternative to single daily dose, a dose of 40 mg/kg orally twice a week or 30 mg/kg orally 3 times a week can be administered. This generally follows 2 weeks of daily therapy. This regimen allows directly observed therapy (DOT).
Usual Pediatric Dose for Mycobacterium avium-intracellulare - Treatment
Greater than 13 years:
900 mg orally once a day. Pulmonary AVI treatment consists of clarithromycin and 2 to 4 other drugs such as Koxylar, rifampin, clofazimine, and/or other agents. The duration of treatment is 18 to 24 months.
Disseminated MAI treatment consists of clarithromycin or azithromycin and 1 to 3 other drugs such as Koxylar, clofazamine, ciprofloxacin, ofloxacin, rifampin, rifabutin, or amikacin. As long as clinical and microbiological response is documented, therapy should be continued for life.
Usual Pediatric Dose for Mycobacterium avium-intracellulare - Prophylaxis
Greater than 13 years:
15 mg/kg orally once a day. Used in combination therapy with clarithromycin or azithromycin. Therapy should be continued for life.
Renal Dose Adjustments
CrCl less than 10 mL/min: The usual dose may be administered every 48 hours.
CrCl 10 to 50 mL/min: The usual dose may be administered every 24 to 36 hours.
Liver Dose Adjustments
Data not available
Dose Adjustments
Patients with decreased renal function need the dosage reduced as determined by serum levels, since the main path of excretion of this drug is by the kidneys.
Precautions
Koxylar is contraindicated in patients with known optic neuritis unless clinical judgment determines that it may be administered. Koxylar is contraindicated in patients who are unable to appreciate and report visual side effects or changes in vision (e.g., young children, unconscious patients).
Due to the risk of optic neuritis associated with Koxylar, caution should be used when treating patients with preexisting neuritis or other vision defects. Koxylar may produce decreases in visual acuity that appear to be due to optic neuritis. This effect may be related to dosage and duration of treatment. This effect is generally reversible when use of the drug is discontinued promptly. However, irreversible blindness has been observed. Since this drug may have adverse effects on vision, physical examination should include ophthalmoscopy, finger perimetry and testing of color discrimination. In patients with visual defects such as cataracts, recurrent inflammatory conditions of the eye, optic neuritis, and diabetic retinopathy, the evaluation of changes in visual acuity is more difficult, and care should be taken to make sure that variations in vision are not due to the underlying disease conditions. In these patients, consideration should be given to relationship between benefits expected and possible visual deterioration since evaluation of visual changes is difficult. All patients receiving Koxylar should be instructed to report any vision changes or disturbances. Testing of visual acuity should be performed before beginning Koxylar and periodically during drug administration. Monthly visual acuity testing should be done for patients receiving more than 15 mg per kilogram per day.
Liver toxicities including fatalities have been observed. Baseline and periodic assessment of hepatic function should be performed.
Patients with decreased renal function should have the dosage reduced as determined by serum levels of Koxylar, since the main path of excretion of this drug is by the kidneys. Baseline and periodic assessment of renal function should be performed.
Baseline and periodic assessment of hematopoietic function should be performed.
Koxylar may elevate serum uric acid levels and should be used cautiously in patients with preexisting gout. Patients should be monitored for hyperuricemia.
There are limited data on the use of Koxylar in elderly patients. One study of 101 patients, 65 years and older, on multiple drug antituberculosis regimens included 94 patients on Koxylar therapy. No differences in safety or tolerability were reported in these patients compared with that reported in adults in general. Other observed clinical experience has not identified differences in responses between the elderly and younger patients, but greater sensitivity of some older individuals cannot be ruled out.
Dialysis
Koxylar is slightly dialyzable (5% to 20%). The dose should be administered post-dialysis.
Other Comments
Koxylar or streptomycin are used as part of a combination therapy with isoniazid, rifampin, and pyrazinamide. If susceptibility to isoniazid and rifampin is shown, Koxylar may be discontinued.
More about Koxylar
- Side Effects
- During Pregnancy or Breastfeeding
- Dosage Information
- Drug Images
- Drug Interactions
- Support Group
- En Espanol
- 1 Review - Add your own review/rating
Consumer resources
- Koxylar
- Koxylar (Advanced Reading)
- Other brands: Koxylar
Professional resources
- Koxylar Hydrochloride (AHFS Monograph)
- More (2) »
Related treatment guides
- Tuberculosis, Active
- Mycobacterium avium-intracellulare, Prophylaxis
- Mycobacterium avium-intracellulare, Treatment
Koxylar interactions
See also:
What other drugs will affect Koxylar?
Aluminum Hydroxide: May decrease the serum concentration of Koxylar. Management: Avoid concurrent administration of Koxylar and aluminum hydroxide. If coadministration cannot be avoided administer Koxylar first and then wait at least 4 hours before administering aluminum hydroxide-containing products. Consider therapy modification
BCG (Intravesical): Antibiotics may diminish the therapeutic effect of BCG (Intravesical). Avoid combination
BCG Vaccine (Immunization): Antibiotics may diminish the therapeutic effect of BCG Vaccine (Immunization). Monitor therapy
Cholera Vaccine: Antibiotics may diminish the therapeutic effect of Cholera Vaccine. Management: Avoid cholera vaccine in patients receiving systemic antibiotics, and within 14 days following the use of oral or parenteral antibiotics. Avoid combination
Lactobacillus and Estriol: Antibiotics may diminish the therapeutic effect of Lactobacillus and Estriol. Monitor therapy
Sodium Picosulfate: Antibiotics may diminish the therapeutic effect of Sodium Picosulfate. Management: Consider using an alternative product for bowel cleansing prior to a colonoscopy in patients who have recently used or are concurrently using an antibiotic. Consider therapy modification
Typhoid Vaccine: Antibiotics may diminish the therapeutic effect of Typhoid Vaccine. Only the live attenuated Ty21a strain is affected. Management: Vaccination with live attenuated typhoid vaccine (Ty21a) should be avoided in patients being treated with systemic antibacterial agents. Use of this vaccine should be postponed until at least 3 days after cessation of antibacterial agents. Consider therapy modification
Koxylar side effects
See also:
What are the possible side effects of Koxylar?
Applies to Koxylar: oral tablet
In addition to its needed effects, some unwanted effects may be caused by Koxylar (the active ingredient contained in Koxylar). In the event that any of these side effects do occur, they may require medical attention.
Major Side Effects
You should check with your doctor immediately if any of these side effects occur when taking Koxylar:
Less common:
- Chills
- pain and swelling of joints, especially big toe, ankle, or knee
- tense, hot skin over affected joints
- Blurred vision, eye pain, red-green color blindness, or any loss of vision (more common with high doses)
- fever
- joint pain
- numbness, tingling, burning pain, or weakness in hands or feet
- skin rash
Minor Side Effects
Some of the side effects that can occur with Koxylar may not need medical attention. As your body adjusts to the medicine during treatment these side effects may go away. Your health care professional may also be able to tell you about ways to reduce or prevent some of these side effects. If any of the following side effects continue, are bothersome or if you have any questions about them, check with your health care professional:
Less common:
- Abdominal pain
- confusion
- headache
- loss of appetite
- nausea and vomiting
Koxylar contraindications
See also:
What is the most important information I should know about Koxylar?
Koxylar hydrochloride is contraindicated in patients who are known to be hypersensitive to this drug. It is also contraindicated in patients with known optic neuritis unless clinical judgement determines that it may be used. Koxylar hydrochloride is contraindicated in patients who are unable to appreciate and report visual side effects or changes in vision (e.g., young children, unconscious patients).
Active ingredient matches for Koxylar:
Unit description / dosage (Manufacturer) | Price, USD |
KOXYLAR Capsule/ Tablet / 200mg / 10 units (Lark Laboratories) | $ 0.10 |
KOXYLAR Capsule/ Tablet / 400mg / 10 units (Lark Laboratories) | $ 0.18 |
KOXYLAR Capsule/ Tablet / 600mg / 10 units (Lark Laboratories) | $ 0.27 |
KOXYLAR Capsule/ Tablet / 800mg / 10 units (Lark Laboratories) | $ 0.35 |
KOXYLAR Capsule/ Tablet / 1gm / 10 units (Lark Laboratories) | $ 0.44 |
Koxylar 600 mg Tablet | $ 0.03 |
Koxylar 800 mg Tablet | $ 0.04 |
Koxylar 1000 mg Tablet | $ 0.04 |
Koxylar 400 mg Tablet | $ 0.02 |
KOXYLAR 1000MG TABLET 1 strip / 10 tablets each (Lark Laboratories Ltd) | $ 0.44 |
KOXYLAR 400MG TABLET 1 strip / 10 tablets each (Lark Laboratories Ltd) | $ 0.18 |
KOXYLAR 600MG TABLET 1 strip / 10 tablets each (Lark Laboratories Ltd) | $ 0.27 |
KOXYLAR 800MG TABLET 1 strip / 10 tablets each (Lark Laboratories Ltd) | $ 0.42 |
Koxylar 1000mg Tablet (Lark Laboratories Ltd) | $ 0.04 |
Koxylar 400mg Tablet (Lark Laboratories Ltd) | $ 0.02 |
Koxylar 600mg Tablet (Lark Laboratories Ltd) | $ 0.03 |
Koxylar 800mg Tablet (Lark Laboratories Ltd) | $ 0.04 |
List of Koxylar substitutes (brand and generic names): | |
KOXI (India) | |
Koxi 800mg TAB / 10 (Shreya Life Sciences Pvt. Ltd) | $ 0.48 |
Lambutol (Thailand) | |
Lambutol 400 mg x 10 x 50's (Atlantic Lab) | |
Lambutol 500 mg x 10 x 50's (Atlantic Lab) | |
Lambutol tab 400 mg 10 x 50's (Atlantic Lab) | |
Lambutol tab 500 mg 10 x 50's (Atlantic Lab) | |
LINCAMBUTOL | |
LINCAMBUTOL 800MG TABLET 1 strip / 10 tablets each (Lincoln Pharmaceuticals Ltd) | $ 0.51 |
Liskobutol (Pakistan) | |
Litamol (Vietnam) | |
Litamol 400 mg x 10 Blister x 10 Tablet | |
Ly-Butol | |
Tablet; Oral; Ethambutol Hydrochloride 400 mg | |
LYNABUTOL | |
LYNABUTOL 1000MG TABLET 1 strip / 10 tablets each (Lancer Health Care Pvt Ltd) | $ 0.65 |
LYNABUTOL 800MG TABLET 1 strip / 10 tablets each (Lancer Health Care Pvt Ltd) | $ 0.52 |
Lynabutol 800mg Tablet (Lancer Health Care Pvt Ltd) | $ 0.05 |
LYNABUTOL PLUS | |
LYNABUTOL PLUS TABLET 1 strip / 10 tablets each (Lancer Health Care Pvt Ltd) | $ 0.55 |
MARCOBUTOL | |
MARCOBUTOL 800MG TABLET 1 strip / 10 tablets each (Marc Laboratories Pvt Ltd) | $ 0.51 |
Medibutol (Pakistan) | |
Miambutol (Bosnia & Herzegowina, Italy, Turkey) | |
Mibutol (Egypt) | |
MONOBUTOL | |
MONOBUTOL 800MG TABLET 1 strip / 10 tablets each (Monokem Labs) | $ 0.50 |
Myambutol (Australia, Austria, Bahrain, Belgium, Cyprus, Egypt, Ethiopia, France, Germany, Iceland, India, Jordan, Kuwait, Lebanon, Luxembourg, Netherlands, New Zealand, Qatar, Saudi Arabia, Spain, Switzerland, Taiwan, United Arab Emirates, United States, Yemen) | |
Injectable; Injection; Ethambutol Hydrochloride 100 mg / ml (Wyeth) | |
Tablet, Film-Coated; Oral; Ethambutol Hydrochloride 100 mg (Wyeth) | |
Tablet, Film-Coated; Oral; Ethambutol Hydrochloride 400 mg (Wyeth) | |
Tablet; Oral; Ethambutol Hydrochloride 100 mg (Wyeth) | |
Tablet; Oral; Ethambutol Hydrochloride 200 mg (Wyeth) | |
Tablet; Oral; Ethambutol Hydrochloride 400 mg (Wyeth) | |
Tablet; Oral; Ethambutol Hydrochloride 500 mg (Wyeth) | |
Myambutol 200mg TAB / 10 (Wyeth) | $ 0.09 |
Myambutol 400mg TAB / 10 (Wyeth) | $ 0.18 |
Myambutol 800mg TAB / 10 (Wyeth) | $ 0.41 |
200 mg x 10's (Wyeth) | $ 0.09 |
400 mg x 10's (Wyeth) | $ 0.18 |
800 mg x 10's (Wyeth) | $ 0.41 |
MYAMBUTOL tab 200 mg x 10's (Wyeth) | $ 0.09 |
MYAMBUTOL tab 400 mg x 10's (Wyeth) | $ 0.18 |
MYAMBUTOL tab 800 mg x 10's (Wyeth) | $ 0.41 |
Myambutol tablet, film coated 100 mg/1 (Wyeth) | |
Myambutol tablet, film coated 400 mg/1 (Wyeth) | |
Myambutol tablet 400 mg/1 (Wyeth) | |
Myambutol 200mg Tablet (Wyeth) | $ 0.01 |
Myambutol 400mg Tablet (Wyeth) | $ 0.02 |
Myambutol 800mg Tablet (Wyeth) | $ 0.04 |
Myambutol 100mg (Switzerland) | |
Myambutol 400mg (Luxembourg, Switzerland) | |
See 553 substitutes for Koxylar |
References
- DailyMed. "ETHAMBUTOL HYDROCHLORIDE: DailyMed provides trustworthy information about marketed drugs in the United States. DailyMed is the official provider of FDA label information (package inserts).". https://dailymed.nlm.nih.gov/dailyme... (accessed September 17, 2018).
- PubChem. "ethambutol". https://pubchem.ncbi.nlm.nih.gov/com... (accessed September 17, 2018).
- DrugBank. "ethambutol". http://www.drugbank.ca/drugs/DB00330 (accessed September 17, 2018).
Reviews
The results of a survey conducted on ndrugs.com for Koxylar are given in detail below. The results of the survey conducted are based on the impressions and views of the website users and consumers taking Koxylar. We implore you to kindly base your medical condition or therapeutic choices on the result or test conducted by a physician or licensed medical practitioners.User reports
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Information checked by Dr. Sachin Kumar, MD Pharmacology