Product image of Myambutol (Ethambutol Hydrochloride) supplied by GNH India

Myambutol

Active Ingredient:
Ethambutol Hydrochloride
Origin:
EU

Myambutol (Ethambutol Hydrochloride)

Ethambutol Hydrochloride, the active ingredient in Myambutol, is an antimyobacterial presented as an oral dosage form for systemic use. It is employed in the treatment of tuberculosis, typically as part of combination therapy, and is indicated for patients with active Mycobacterium tuberculosis infection.

GNH India supplies Myambutol as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable sourcing for global health programmes, including public and private sector purchasers.

Manufacturer / TM Owner

Teofarma S.R.L.

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Indications & Clinical Uses

Ethambutol is an antitubercular agent used in combination regimens targeting Mycobacterium tuberculosis infections.

  • Pulmonary tuberculosis: contributes to bacterial clearance when combined with other first‑line drugs.
  • Extrapulmonary tuberculosis: aids in treating disease sites such as lymph nodes, pleura, or meninges as part of multidrug therapy.
  • Miliary tuberculosis: provides bacteriostatic activity across disseminated infection when used in standard combination protocols.

How It Works

  • Ethambutol inhibits the arabinosyl transferase enzyme involved in arabinogalactan synthesis, a key component of the mycobacterial cell wall. By blocking this pathway, the drug reduces cell wall integrity, leading to a bacteriostatic effect against Mycobacterium tuberculosis. The inhibition is selective for mycobacteria, allowing it to be used safely in combination with other antitubercular agents.

Side Effects

Ethambutol may cause a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Visual disturbances (blurred vision, color vision changes)
  • Nausea
  • Vomiting
  • Abdominal pain
  • Headache
  • Rash

Serious or Rare Side Effects

  • Optic neuritis leading to permanent vision loss
  • Severe allergic reactions including anaphylaxis
  • Hepatic dysfunction (elevated transaminases, hepatitis)
  • Peripheral neuropathy
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis
  • Severe dizziness or loss of coordination

Precautions & Warnings

When prescribing Ethambutol, clinicians should observe several precautionary measures to minimize risk.

  • Baseline visual assessment: perform ophthalmologic exam before therapy and monitor periodically.
  • Renal function monitoring: adjust dose in patients with impaired clearance.
  • Hepatic impairment: use with caution and monitor liver enzymes.
  • Known hypersensitivity: avoid in patients with documented allergy to ethambutol.
  • Elderly patients: start at lower dose and observe for toxicity.
  • Store at room temperature: keep in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Ethambutol can interact with several medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Isoniazid: increased risk of optic neuritis when combined.
  • Rifampicin: reduces ethambutol plasma concentrations, potentially decreasing effectiveness.
  • Streptomycin: heightened neurotoxic potential when used together.

Moderate Interactions (Monitor Closely)

  • Pyrazinamide: may increase hepatotoxic risk.
  • Fluoroquinolones: additive risk of tendon disorders.
  • Antiretroviral agents (e.g., protease inhibitors): may affect drug levels.
  • Diuretics: can exacerbate electrolyte disturbances.
  • Vitamin supplements (pyridoxine): monitor for overlapping toxicity.

Frequently Asked Questions

Myambutol contains ethambutol hydrochloride, which is used as part of multidrug therapy to treat active tuberculosis infection. It is prescribed together with other first‑line antitubercular agents to improve bacterial clearance and reduce the risk of resistance.

Ethambutol blocks the arabinosyl transferase enzyme that synthesizes arabinogalactan, an essential component of the mycobacterial cell wall. This inhibition weakens the wall, producing a bacteriostatic effect that limits the growth of Mycobacterium tuberculosis.

The dose of Myambutol is determined by the prescribing clinician based on the patient’s age, weight, renal function and the overall treatment regimen. Standard adult dosing ranges are established in clinical guidelines, but the exact amount and schedule must be individualized by a qualified health professional.

Safety data for ethambutol in pregnancy and lactation are limited. The drug should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision must be made by the treating physician.

To request Myambutol, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Ethambutol differs from agents such as isoniazid or rifampicin by targeting cell‑wall arabinogalactan synthesis rather than mycolic acid production or RNA synthesis. It is generally well tolerated but requires regular visual monitoring, whereas some alternatives have higher hepatotoxic or neurotoxic profiles.

Myambutol should be stored at room temperature, below 25 °C, in its original container. Protect the product from moisture, direct sunlight and extreme temperatures to maintain potency throughout its shelf life.

Myambutol is taken orally, usually with a glass of water. It can be administered with or without food, but patients should follow the prescribing clinician’s instructions regarding timing and any dietary considerations.

The most critical adverse effects include optic neuritis, which can cause irreversible vision loss, severe allergic reactions such as anaphylaxis, and hepatic dysfunction. Patients should report any visual changes, rash, jaundice or unexplained fatigue to their healthcare provider promptly.

Myambutol is contraindicated in individuals with a known hypersensitivity to ethambutol or any component of the formulation. Caution is also advised for patients with severe renal impairment, as dose adjustment may be required, and for those with pre‑existing optic disorders.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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