Nifurtimox — Active Pharmaceutical Ingredient

Nifurtimox is an active pharmaceutical ingredient found in 1 FDA-approved drug product. Forms: TABLET. Routes: ORAL.

This content is for informational purposes only. Always consult a healthcare professional.

Nifurtimox (1 brand name, 1 dosage form, 1 route)

Available dosage forms: TABLET.

Routes of administration: ORAL.

Brand Names

  • LAMPIT

Indications and Usage

LAMPIT is indicated in pediatric patients (birth to less than 18 years of age and weighing at least 2.5 kg) for the treatment of Chagas disease (American Trypanosomiasis) caused by Trypanosoma cruzi [see Clinical Studies (14)].

Contraindications

LAMPIT tablets are contraindicated in: •Patients with known hypersensitivity to nifurtimox or any of the excipients in LAMPIT [see Warnings and Precautions (5.4)]. •Patients who consume alcohol during treatment [see Drug Interactions (7)]

Adverse Reactions

The following serious or otherwise important adverse reactions are discussed elsewhere in the labeling: •Potential for Genotoxicity, Carcinogenicity, and Mutagenicity [see Warnings and Precautions (5.1)] •Worsening of Neurological and Psychiatric Conditions [see Warnings and Precautions (5.3)] •Hypersensitivity [see Warnings and Precautions (5.4)] •Decreased Appetite and Weight Loss [see Warnings and Precautions (5.5)] •Porphyria [see Warnings and Precautions (5.6)]

Drug Interactions

Concomitant use of LAMPIT with alcohol may increase the incidence and severity of undesirable effects similar to other nitrofurans and nitroheterocyclic compounds. LAMPIT is contraindicated in patients who consume alcohol during treatment [see Dosage and Administration (2.2) Contraindications (4)].

Mechanism of Action

Nifurtimox is an antiprotozoal drug [see Microbiology (12.4)].

⚠ Caution
Medical Disclaimer: This information is for educational purposes only. Always consult a healthcare professional before taking any medication.