Lampit

Lampit Uses, Dosage, Side Effects, Food Interaction and all others data.

Chagas disease, caused by a parasite known as Trypanosoma cruzi (T.cruzi), is a vector-transmitted disease affecting animals and humans in the Americas. It is commonly known as American Trypanosomiasis.

The CDC estimates that approximately 8 million people in Central America, South America, and Mexico are infected with T. cruzi, without symptoms. If Chagas disease is left untreated, life-threatening sequelae may result.

Lampit, developed by Bayer, is a nitrofuran antiprotozoal drug used in the treatment of Chagas disease. On August 6 2020, accelerated FDA approval was granted for its use in pediatric patients in response to promising results from phase III clinical trials. Continued approval will be contingent upon confirmatory data. A convenient feature of Bayer's formulation is the ability to divide the scored tablets manually without the need for pill-cutting devices.

Lampit
Uses
Dosage
Side Effect
Precautions
Interactions
Uses during Pregnancy
Uses during Breastfeeding
Accute Overdose
Food Interaction
Half Life
Volume of Distribution
Clearance
Interaction With other Medicine
Contradiction
Storage

Trade Name	Lampit
Availability	Prescription only
Generic	Nifurtimox
Nifurtimox Other Names	Nifurtimox, Nifurtimoxum
Related Drugs	pentamidine, benznidazole, fexinidazole, Lampit, Nebupent
Weight	120mg, 30mg,
Type	Oral tablet
Formula	C₁₀H₁₃N₃O₅S
Weight	Average: 287.29 Monoisotopic: 287.057591705
Protein binding	The plasma protein binding of nifurtimox is approximately 42%. It is primarily bound to albumin.
Groups	Approved, Investigational
Therapeutic Class
Manufacturer
Available Country	United States,
Last Updated:	September 19, 2023 at 7:00 am

Uses

Lampit is an antiparasitic drug used for the treatment of Chagas disease (Trypanosoma cruzi infection).

Lampit is indicated in pediatric patients under 18 weighing at least 2.5 kg. Continued approval of this drug for this indication is dependent upon confirmatory clinical trial results.

Lampit is also used to associated treatment for these conditions: Chagas Disease

How Lampit works

The mechanism of action of nifurtimox has not been fully elucidated, however, is believed to occur by the activation of nitroreductase enzymes that produce reactive metabolites with a series of deleterious effects on Trypanosoma cruzi, the parasite causing Chagas disease. The antiprotozoal actions of nifurtimox occur both intracellularly and extracellularly. Inhibition of parasite dehydrogenase activity is another purported mode of action of nifurtimox that warrants further research.

Toxicity

There is limited information in the literature regarding overdose with nifurtimox. Some symptoms of nifurtimox toxicity may include weight loss, anorexia, nausea, vomiting, vertigo, headache, nervous excitation, insomnia, convulsions, drowsiness, arthralgias, myalgias, disorientation, abdominal pain, mucosal edema, and skin manifestations. These symptoms are adverse effects of nifurtimox and are likely to be exaggerated with increased exposure.

Food Interaction

Avoid alcohol. Alcohol use during nifurtimox treatment may increase undesirable adverse effects.
Take with food.

[Major] CONTRAINDICATED: Use of alcohol or products containing alcohol during therapy with nitrofurans may result in a disulfiram-like reaction in some patients.

The presumed mechanism is inhibition of aldehyde dehydrogenase (ALDH) by nitrofurans in a manner similar to disulfiram.

Following ingestion of alcohol, inhibition of ALDH results in increased concentrations of acetaldehyde, the accumulation of which can produce an unpleasant physiologic response referred to as the 'disulfiram reaction'.

Symptoms include flushing, throbbing in head and neck, throbbing headache, respiratory difficulty, nausea, vomiting, sweating, thirst, chest pain, palpitation, dyspnea, hyperventilation, tachycardia, hypotension, syncope, weakness, vertigo, blurred vision, and confusion.

Severe reactions may result in respiratory depression, cardiovascular collapse, arrhythmia, myocardial infarction, acute congestive heart failure, unconsciousness, convulsions, and death.

ADJUST DOSING INTERVAL: Food enhances the oral bioavailability of nifurtimox.

When a single 120 mg oral dose of nifurtimox was administered with a high-fat meal (800 to 1000 calories; approximately 60% fat) in adult Chagas patients, nifurtimox peak plasma concentration (Cmax) and systemic exposure (AUC) increased by 68% and 71%, respectively, compared to administration under fasted conditions.

Lampit was administered with food in clinical trials.

MANAGEMENT: Consumption of alcohol is considered contraindicated during nifurtimox therapy.

To ensure maximal oral absorption, nifurtimox should be administered with food.

Volume of Distribution

Lampit crosses the blood-brain barrier and the placenta.

Elimination Route

The average AUC of nifurtimox is estimated between 1676-2670 μg∙h/L. One pharmacokinetic study of healthy volunteers revealed an AUC of 5430 ng∙ml^{-1 Cmax ranges between 425-568 μg/L (26–50%) after a single dose of 20 mg with food in adults. Tmax is 4 hours, ranging from 2 to 8 hours post-dose in the fed state. In a pharmacokinetic study of healthy volunteers, serum concentration was low, likely due to the first-pass effect.}

Half Life

The elimination half-life of nifurtimox ranges from 2.4–3.6 hours. A pharmacokinetic study of healthy volunteers and patients with renal failure revealed respective mean half-lives of 2.95 h and 3.95 h.