Registered Malawi · PMRA

PROTIONAMIDE 250MG TABLET

PROTIONAMIDE

PMPB/PL354/48 TABLET

What it does

Protionamide is a medication used to treat tuberculosis (TB), particularly when other treatments are not effective.

Commonly used for: tuberculosis (TB)

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Plain-language summary for general understanding - not medical advice. Always follow your pharmacist/doctor.

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Answers come only from this medicine's registration record, BNF monograph and interaction data - not medical advice.

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Registration & product details

Registration no.
PMPB/PL354/48
Registration date
23/06/2017
Expiry date
30/06/2020
Status
Registered
Active ingredient
PROTIONAMIDE
Dosage form
TABLET
Strength
-
Pack size
-
Therapeutic class
-
Manufacturer / MAH
-
Applicant / LTR
-
Country of origin
-

Source: Pharmacy and Medicines Regulatory Authority · fetched 2026-04-21 17:37:41 · updated 2026-09-29 04:33:05

Disclaimer: This information is sourced from Pharmacy and Medicines Regulatory Authority (Malawi). Always consult a qualified healthcare professional before using any medication.

About this medicine

Protionamide is a medication used to treat tuberculosis (TB), particularly when other treatments are not effective.

What it treats

  • tuberculosis (TB)

How it works

Protionamide helps kill the bacteria that cause tuberculosis, allowing the body to recover from the infection.

Who it's for

This medication is for people diagnosed with tuberculosis who may need additional treatment options.

AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.

Clinical monograph: protionamide

BNF-referenced

Protionamide is an antitubercular agent used primarily in the treatment of tuberculosis, especially in cases resistant to first-line therapy. It belongs to the class of thioamide derivatives and functions by inhibiting the synthesis of mycolic acids, which are essential components of the mycobacterial cell wall. Protionamide is often used in combination with other antitubercular agents to enhance therapeutic efficacy and reduce the risk of resistance development.

Indications

  • Tuberculosis (TB)
  • Multidrug-resistant tuberculosis (MDR-TB)

Dosage

Children: For children, the dosage should be determined based on weight and clinical guidelines; refer to the BNF for Children for specific dosing recommendations.

Adults: The usual adult dosage is 500 mg to 1000 mg daily, administered in divided doses.

Mechanism of action

Protionamide exerts its effect by inhibiting the enzyme InhA, which is involved in the fatty acid synthesis pathway crucial for the production of mycolic acids in the mycobacterial cell wall. This disruption in mycolic acid synthesis compromises the integrity of the bacterial cell wall, leading to cell lysis and death.

Pharmacodynamics

The pharmacodynamics of protionamide involve its bactericidal activity against Mycobacterium tuberculosis. It shows a time-dependent killing effect, meaning that prolonged exposure to the drug enhances its efficacy. The drug also demonstrates synergistic effects when used in combination with other antitubercular agents, making it a valuable component in multidrug-resistant tuberculosis treatment regimens.

Pharmacokinetics

Protionamide is well absorbed from the gastrointestinal tract, with peak plasma concentrations typically occurring within 2 to 4 hours after administration. It is metabolized in the liver, primarily by N-acetylation, and has a variable half-life of approximately 2 to 8 hours. The drug is excreted mainly in the urine, both as unchanged drug and metabolites. Renal impairment may affect its clearance, necessitating dosage adjustments in such patients.

Adverse effects

  • Nausea
  • Vomiting
  • Anorexia
  • Rash
  • Hepatotoxicity
  • Peripheral neuropathy

Interactions

  • May enhance the effects of other antitubercular agents
  • Potential interaction with isoniazid leading to increased risk of peripheral neuropathy

Precautions

  • Monitor liver function tests during treatment due to potential hepatotoxicity
  • Use with caution in patients with a history of liver disease
  • Regular monitoring for signs of peripheral neuropathy

Pregnancy

Use only if the potential benefit justifies the risk to the fetus. Consult with a healthcare provider.

Breast-feeding

Caution is advised as protionamide is excreted in breast milk. Weigh the benefits against potential risks.

Storage

Store in a cool, dry place away from light. Keep out of reach of children.

Formulations

  • Tablets

AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.

Molecular reference: protionamide

PubChem CID 666418

Molecular formula: C9H12N2S

Source: PubChem (NCBI) · pathways from PathBank, Reactome, WikiPathways & PharmGKB.