Furazolidone is a nitrofuran antimicrobial with antiprotozoal and antibacterial activity historically used for infectious diarrhea, traveler’s diarrhea, and giardiasis. It also exhibits monoamine oxidase inhibitor (MAOI) properties, which means notable food and drug interactions. While effective against certain pathogens, furazolidone is not FDA‑approved in the United States and has been discontinued or restricted in many regions due to evolving safety standards. Any consideration of therapy should involve a licensed clinician, especially given MAOI-related risks, potential hemolysis in G6PD deficiency, and possible adverse effects. Safer, modern alternatives are often preferred, but evidence-based use persists in some settings under medical supervision.
Furazolidone is an older nitrofuran antimicrobial used historically to treat infectious diarrhea, traveler’s diarrhea caused by susceptible bacteria, and protozoal infections such as giardiasis. In the past, it was included in some Helicobacter pylori regimens where resistance to other agents was high. Its spectrum covers select Gram-negative and Gram-positive organisms, as well as Giardia lamblia. Due to safety concerns and the advent of newer, better-tolerated drugs, furazolidone has largely been replaced by alternatives like metronidazole, tinidazole, azithromycin, rifaximin, or fluoroquinolones (depending on local resistance patterns and indications).
It is important to note that furazolidone is not FDA-approved in the United States and is unavailable in many countries. Any use should follow local regulations and current clinical guidelines, with clinicians typically reserving it for specific scenarios where benefits may outweigh risks and where susceptibility data support its use.
Furazolidone is a nitrofuran derivative that undergoes enzymatic reduction inside microbial cells to generate reactive intermediates. These intermediates damage bacterial DNA and disrupt essential metabolic processes, leading to bactericidal or bacteriostatic effects depending on the organism and concentration. Uniquely, furazolidone also functions as a monoamine oxidase inhibitor (MAOI), which is unrelated to its antimicrobial action but clinically significant: MAOI activity can precipitate hypertensive crises with tyramine-rich foods and trigger serious drug–drug interactions, including serotonin syndrome when combined with serotonergic agents.
Dosing varies by indication, local guidelines, product formulation, and patient factors. Because furazolidone is not FDA-approved in the U.S. and is restricted in many countries, do not self-medicate. Discuss any use with a licensed clinician. Historically reported regimens (for educational context) included adult doses of 100 mg four times daily for 5–7 days for certain bacterial diarrheas and 7–10 days for giardiasis. Pediatric dosing where used historically was often weight-based (for example, total daily dose around 7.5 mg/kg/day divided into four doses), but ranges vary and require clinician oversight. Modern therapy frequently favors alternative agents with improved safety profiles.
General administration advice has included taking furazolidone with food to reduce stomach upset and adhering strictly to the full course once prescribed. Because of MAOI effects, patients are instructed to avoid high-tyramine foods and to review all concomitant medications with a pharmacist or clinician before starting therapy and for a period after completion (commonly two weeks) to minimize interaction risks.
Furazolidone’s MAOI activity is the core driver of its precaution profile. Patients must avoid tyramine-rich foods and beverages (such as aged cheeses, cured or fermented meats, soy sauce, miso, tempeh, sauerkraut, kimchi, Marmite/yeast extracts, certain beers, and some red wines) during treatment and for at least 14 days after the last dose to reduce the risk of hypertensive crisis. Concomitant serotonergic or sympathomimetic drugs can cause life-threatening reactions and should generally be avoided.
People with glucose-6-phosphate dehydrogenase (G6PD) deficiency may be at increased risk of hemolytic anemia with nitrofuran derivatives. If a clinician considers furazolidone in a setting where it is available, they should evaluate G6PD status when relevant. Patients with a history of severe drug allergies, hepatic impairment, uncontrolled hypertension, or certain psychiatric conditions may require additional caution. Alcohol should be avoided during therapy and for several days after due to the potential for a disulfiram-like reaction (flushing, nausea, vomiting, tachycardia).
Pregnancy and breastfeeding: Furazolidone has limited contemporary safety data in pregnancy and lactation and is generally avoided when alternatives exist. Discuss risks and benefits with a qualified clinician; safer, guideline-supported options are usually preferred for pregnant or breastfeeding individuals.
Contraindications may include hypersensitivity to furazolidone or other nitrofurans; concurrent use with other MAO inhibitors; recent use of serotonergic agents where an appropriate washout has not occurred; and use with known tyramine sensitivity or inability to adhere to dietary restrictions. Severe hepatic dysfunction, a history of hypertensive crisis related to MAOIs, or catecholamine-secreting tumors (e.g., pheochromocytoma) also warrant avoidance. Individuals with G6PD deficiency are at heightened risk for hemolysis and generally should not receive nitrofuran derivatives unless a specialist deems benefits to outweigh risks and close monitoring is in place.
Common adverse effects include nausea, vomiting, abdominal discomfort, decreased appetite, and diarrhea. Headache, dizziness, and rash or pruritus may occur. Because of its MAOI properties, a sudden severe headache, chest pain, palpitations, neck stiffness, shortness of breath, or marked blood pressure elevation require urgent medical evaluation. Signs of serotonin syndrome (agitation, confusion, fever, sweating, tremor, muscle rigidity, diarrhea) can be life-threatening and demand immediate care if serotonergic agents have been co-administered.
Less common but serious events can include hemolytic anemia (especially in G6PD deficiency), hepatotoxicity, peripheral neuropathy, or hypersensitivity reactions, including angioedema or anaphylaxis. Any jaundice, dark urine, light-colored stools, persistent fatigue, bruising, or bleeding should prompt urgent evaluation. As with other nitrofuran agents, long-term or repeated courses may raise the risk of rare pulmonary or neurological toxicities; such use is not typical with modern practice and should be supervised closely.
Food interactions: Avoid tyramine-rich foods during treatment and for 14 days afterward to reduce the risk of hypertensive crisis. Examples include aged cheeses, cured or fermented meats, fish sauces, soy products (soy sauce, miso, tempeh), fermented vegetables (sauerkraut, kimchi), yeast extracts, some beers (especially draft), and certain red wines.
Alcohol: Avoid alcohol during therapy and for several days after due to potential disulfiram-like reactions (flushing, throbbing headache, nausea/vomiting, tachycardia) and additive blood pressure effects.
Drug interactions: Due to MAOI effects, combining furazolidone with serotonergic agents (SSRIs like fluoxetine/sertraline, SNRIs like venlafaxine/duloxetine, TCAs, MAOIs, mirtazapine, buspirone, tramadol, meperidine, methadone, linezolid, methylene blue, triptans, St. John’s wort, and dextromethorphan) can precipitate serotonin syndrome and is generally contraindicated. Sympathomimetics (pseudoephedrine, phenylephrine, ephedrine), many stimulant medications, and certain weight-loss supplements can trigger dangerous hypertension with MAOIs and should be avoided. Always give your clinician and pharmacist a complete medication and supplement list, including over-the-counter remedies and herbal products.
If a dose is missed, take it as soon as you remember unless it is close to the time for the next dose. If it is nearly time for your next scheduled dose, skip the missed dose and resume your regular dosing schedule. Do not double up to make up for a missed dose. Because interaction risks are significant, do not restart or stop furazolidone without discussing it with a clinician, and continue to follow dietary and drug-interaction precautions during therapy and for two weeks after the last dose.
Suspected overdose is a medical emergency. Call local emergency services or your poison control center immediately. Symptoms may include severe nausea and vomiting, agitation, confusion, tremor, fever, rapid heartbeat, severe hypertension or hypotension, seizures, and signs of serotonin syndrome. Management is supportive, with close monitoring of airway, breathing, circulation, temperature, and blood pressure. Activated charcoal may be considered if presentation is early and the airway is protected. Because of MAOI properties, avoid agents that can worsen hypertension or serotonergic toxicity unless directed by specialists.
Store furazolidone tablets or suspensions in a tightly closed, child-resistant container at controlled room temperature (generally 20–25°C or 68–77°F), protected from excess heat, moisture, and light. Do not store in a bathroom. Keep out of reach of children and pets. Do not use past the printed expiration date, and discard any unused reconstituted suspension according to the product’s instructions. Never share antibiotics with others, and return or dispose of leftover medication via approved take-back programs where available.
In the United States, furazolidone is not FDA-approved and is not marketed domestically. U.S. law requires a valid prescription for dispensing prescription medications and imposes strict standards on sourcing and quality. HealthSouth Rehabilitation Hospital of Las Vegas operates within these regulations. While many customers search for ways to “buy furazolidone without a prescription,” our pharmacy provides a legal, structured alternative: a pharmacist-guided intake that, when clinically appropriate and lawful in your jurisdiction, routes your case to a licensed prescriber for evaluation. If a prescriber determines that furazolidone (or a safer, guideline-recommended alternative) is appropriate, a valid prescription is issued before any dispensing or fulfillment.
This means you do not need to bring a traditional paper prescription from an outside clinic—your order is supported by an integrated, compliant clinician review. Where furazolidone is unavailable or not recommended, we help identify evidence-based alternatives (for example, metronidazole or tinidazole for giardiasis, rifaximin or azithromycin for certain traveler’s diarrhea scenarios, as guided by local resistance patterns). Our team prioritizes medication quality, patient safety, and regulatory compliance, with transparent sourcing, secure checkout, and responsive support. If the medication must be fulfilled through international channels, we observe all applicable laws and will only proceed when it is lawful and clinically justified.
Important: Because furazolidone has MAOI-related risks and significant interactions, a licensed clinician’s oversight is essential. Avoid unverified online sellers that offer prescription drugs without clinician review; counterfeit or substandard products can be dangerous. HealthSouth Rehabilitation Hospital of Las Vegas’s structured process is designed to protect you—ensuring that the right therapy, dosage, and interaction checks are applied before any medicine reaches you.
Furazolidone is an oral nitrofuran antimicrobial with antiprotozoal activity and mild monoamine oxidase inhibitor (MAOI) properties, historically used for infectious diarrhea and giardiasis; it is unavailable or restricted in many countries due to safety concerns.
Depending on local guidelines, it has been used for acute infectious diarrhea caused by susceptible bacteria, giardiasis, and as part of certain Helicobacter pylori regimens, though it is not first-line in many regions.
It is reduced by microbial nitroreductases to reactive intermediates that damage DNA and other macromolecules, killing susceptible bacteria and protozoa; it also exhibits MAOI activity that drives many food and drug interactions.
Availability varies by country; it is not marketed in the United States and European Union, but may be available by prescription in some regions where local authorities deem the benefits to outweigh risks for specific indications.
Nausea, vomiting, abdominal discomfort, headache, dizziness, and rash are most frequently reported; taking it with food may ease stomach upset if your clinician approves.
Stop the drug and seek care for signs of allergy (hives, swelling, breathing trouble), unexplained bruising or pallor (possible hemolysis, especially in G6PD deficiency), severe abdominal pain, dark urine with jaundice (liver injury), neuropathy, or severe headache with palpitations after tyramine-rich foods.
People with known hypersensitivity to nitrofurans, G6PD deficiency, significant hepatic or renal impairment, infants, and generally pregnant or breastfeeding individuals unless no safer alternatives exist and a specialist advises otherwise.
No; alcohol can trigger a disulfiram-like reaction with flushing, cramping, nausea, vomiting, and hypotension—avoid alcohol during therapy and for at least a few days after the last dose.
Because of MAOI effects, avoid tyramine-rich foods (aged cheeses, cured meats, fermented soy products, sauerkraut, draft beers), which can precipitate hypertensive crisis; check with your clinician for a comprehensive list.
Avoid combining with serotonergic antidepressants (SSRIs, SNRIs, TCAs), other MAOIs, linezolid, meperidine, tramadol, dextromethorphan, stimulants, and decongestants like pseudoephedrine; always provide a full medication list to your prescriber.
It is generally avoided in pregnancy and lactation due to limited human safety data and potential risks; if benefits might outweigh risks, decisions should be individualized by an experienced clinician.
Pediatric use is restricted to specific indications like giardiasis in some regions and requires weight-based prescribing by a clinician; it should not be used in very young infants.
Many patients notice improvement within 24–72 hours, but you should complete the prescribed course even if symptoms improve to reduce relapse and resistance.
Take it when you remember unless it is close to the next dose; if so, skip the missed dose and resume your usual schedule—do not double up.
Any antimicrobial can select for resistance; judicious, guideline-based use and completing the full course as prescribed help limit resistance development.
In some regions with metronidazole resistance or intolerance, furazolidone-containing regimens are considered; selections should follow local resistance patterns and specialist guidance.
Keep it in its original container at room temperature away from moisture and heat, and out of reach of children and pets.
It can confound catecholamine-related measurements due to MAOI activity; tell your laboratory and clinicians you are taking it so results are interpreted correctly.
Follow your clinician’s instructions precisely, take doses at evenly spaced intervals, avoid interacting foods and drugs, and do not stop early unless your prescriber directs you to.
No; it is a prescription-only medicine where marketed, and in many countries it is not available at all.
Both are nitrofuran antibiotics, but nitrofurantoin concentrates in urine and is used for lower urinary tract infections, while furazolidone acts systemically in the gut for certain diarrheal diseases and giardiasis; furazolidone has MAOI interactions that nitrofurantoin lacks.
Nifuroxazide is minimally absorbed and works locally in the gut with fewer systemic side effects and interactions, whereas furazolidone is absorbed, has broader systemic effects, and carries MAOI-related food and drug restrictions.
“Stronger” depends on the target; furazolidone may be preferred for some enteric pathogens and protozoa, while nitrofurantoin is superior for E. coli bladder infections—each fits different niches based on pharmacokinetics and susceptibility.
Nitrofurazone (nitrofural) is a topical nitrofuran for skin and wound infections, while furazolidone is oral for intestinal infections; the choice depends on infection site and clinician guidance.
Nifuratel is a nitrofuran derivative used in some countries for gynecologic infections and giardiasis with less MAOI concern, whereas furazolidone’s primary role is enteric infections and it requires MAOI precautions; availability varies by region.
Both are nitrofurans with historical veterinary and limited human use, but furaltadone is largely obsolete and banned in food animals; neither should be interchanged without explicit, locally compliant medical guidance.
Nifuroxazide’s limited absorption often yields fewer systemic adverse effects and interactions, making it attractive for mild cases in regions where it is approved; furazolidone may be considered for specific pathogens but requires stricter interaction precautions.
Both nitrofurans can cause hemolysis in G6PD deficiency; they are generally avoided or used with extreme caution and close monitoring in affected individuals.
Furazolidone, due to MAOI activity, has substantially more interaction risks with serotonergic agents, sympathomimetics, dextromethorphan, and tyramine-rich foods; nitrofurantoin’s interaction profile is comparatively modest.
Where approved, nifuroxazide’s low systemic absorption may be favored for uncomplicated diarrhea; furazolidone may be used for specific pathogens like Giardia under pediatric specialist guidance and with careful monitoring for interactions.
Resistance patterns differ by pathogen and setting; nitrofurantoin retains activity against many urinary E. coli strains, while furazolidone can be effective against certain enteric bacteria and protozoa, but local susceptibility data should guide therapy.
Furazolidone uniquely requires tyramine restrictions among commonly used nitrofurans; nitrofurantoin, nifuroxazide, and nitrofurazone do not have clinically relevant MAOI effects.