last update: November 14, 2025
Isoniazid (often abbreviated INH) is a first-line antibacterial medicine used to treat and prevent tuberculosis (TB) caused by Mycobacterium tuberculosis. It is a cornerstone of TB therapy because it kills actively dividing TB bacteria and helps sterilize latent organisms. For active TB disease, isoniazid must always be used in combination with other anti-tubercular medications to prevent resistance and achieve cure. For latent TB infection (LTBI), isoniazid may be used as a single agent in certain regimens to reduce the risk of developing active disease.
Note on historical confusion: An older TB medicine called iproniazid (not isoniazid) had antidepressant properties. Isoniazid itself is not an antidepressant and should not be used for mood disorders.
Use isoniazid exactly as directed by your healthcare provider. Dosing, duration, and companion medicines depend on whether you are treating active TB disease or latent TB infection.
Isoniazid is a prodrug that must be activated by the bacterial enzyme KatG inside Mycobacterium tuberculosis. Once activated, it inhibits the synthesis of mycolic acids, essential components of the mycobacterial cell wall. This disruption leads to bacterial death or growth arrest. Genetic mutations in bacterial targets (such as katG or inhA) can confer isoniazid resistance, which is why combination therapy is critical for active disease.
Follow local or national TB guidelines and your clinician’s instructions. Typical adult and pediatric dosing frameworks include:
Your healthcare provider will determine the best regimen based on factors such as drug susceptibility, comorbid conditions, potential drug interactions, and adherence considerations. Never change your dose or schedule without medical guidance.
Contact your clinician immediately if any of these apply to you or if you are unsure whether you can take isoniazid safely.
Isoniazid is metabolized in the liver and can inhibit several cytochrome P450 enzymes, potentially increasing blood levels of other drugs. Rifampin, commonly co-administered in TB regimens, induces liver enzymes and can alter levels of many medicines. Always provide your healthcare team with a complete medication list.
This is not a complete list of interactions. Always check with your healthcare provider before starting, stopping, or changing any medication while on isoniazid.
Many people tolerate isoniazid well. Side effects, when they occur, are often mild and manageable. Contact your healthcare provider if side effects persist, worsen, or concern you.
This is not a complete list of side effects. If you suspect a serious reaction, stop the medication and seek urgent medical care.
Overdose can be life-threatening and may present with nausea, vomiting, dizziness, seizures, metabolic acidosis, and coma. This is a medical emergency. Call emergency services immediately. In a clinical setting, treatment may include activated charcoal, seizure control, supportive care, and intravenous pyridoxine.
In the United States, isoniazid is a prescription-only medication regulated by federal and state laws. Most patients obtain isoniazid through a licensed prescriber, often in partnership with public health departments that oversee TB control and support adherence, monitoring, and safety. Some programs dispense isoniazid under physician-directed protocols or standing orders, including directly observed therapy (DOT) models. These structured pathways ensure clinician oversight, appropriate screening, and monitoring even when a traditional paper prescription is not individually issued to the patient.
HealthSouth Rehabilitation Hospital of Petersburg offers a legal and structured solution for acquiring isoniazid without a formal prescription by operating under compliant clinical protocols and licensed provider oversight. Eligibility screening, verification of clinical need, and ongoing monitoring are incorporated to meet safety, quality, and regulatory standards. Patients should consult their clinician or local public health department to determine the most appropriate, lawful avenue for obtaining isoniazid and to ensure that all care, monitoring, and follow-up align with U.S. regulations and best practices.
Isoniazid is a first-line antibiotic for tuberculosis that targets the mycobacterial cell wall. After activation by the bacterial enzyme KatG, it inhibits enzymes needed to make mycolic acids, slowing or killing Mycobacterium tuberculosis.
Isoniazid treats active tuberculosis as part of combination therapy and prevents tuberculosis by treating latent TB infection. It is used in adults and children per public health guidelines.
Take isoniazid on an empty stomach, 1 hour before or 2 hours after food. Avoid aluminum-containing antacids within 2 hours of a dose because they reduce absorption.
Many people benefit from pyridoxine 25–50 mg daily to prevent peripheral neuropathy. It is especially recommended if you are pregnant, breastfeeding, have diabetes, HIV, renal failure, malnutrition, alcohol use, are older, or take seizure medicines.
Common effects include nausea, upset stomach, loss of appetite, mild fatigue, and tingling in hands or feet. Most are manageable and often improve over time.
Signs of liver injury include persistent nausea, vomiting, abdominal pain, dark urine, pale stools, jaundice, or severe fatigue—seek medical care promptly. Severe peripheral neuropathy, rash, fever, or unexplained bruising also require urgent evaluation.
Your clinician may check baseline liver function tests, especially if you are over 35, drink alcohol, are pregnant or postpartum, or have liver disease or HIV. Periodic monitoring is advised for those at higher risk or if symptoms develop.
Isoniazid can raise levels of phenytoin, carbamazepine, valproate, and warfarin, increasing toxicity or bleeding risk. It can also interact with disulfiram and certain antiretrovirals; always share your medication list with your clinician.
Limit foods high in tyramine or histamine—aged cheeses, cured meats, red wine, some fish (e.g., tuna, sardines)—which can cause flushing, headache, or palpitations. Avoid alcohol to reduce the risk of hepatotoxicity.
Yes, you can take it with a light snack to reduce nausea, but avoid aluminum-containing antacids around the same time. Consistency in timing helps maintain steady levels.
Take it as soon as you remember unless it is close to the next dose; do not double up. For directly observed therapy schedules, contact your clinic for guidance.
For latent TB, common regimens are 6 or 9 months of daily isoniazid. For active TB, isoniazid is used with other drugs for at least 6 months, adjusted based on response and susceptibility.
Isoniazid can deplete vitamin B6, affecting nerve function and leading to peripheral neuropathy. Taking pyridoxine and managing risk factors greatly reduces this risk.
Some people report irritability, insomnia, or mood changes. Persistent or severe symptoms should be discussed with your clinician to rule out interactions or rare neurotoxic effects.
Keep tablets tightly closed at room temperature, away from moisture and heat, and out of reach of children. Do not use past the expiration date.
It is best to avoid alcohol because it significantly increases the risk of isoniazid-related liver injury. Even moderate drinking can compound hepatotoxicity.
Isoniazid is widely used in pregnancy when benefits outweigh risks, particularly for latent TB or high-risk exposure. Pyridoxine supplementation and liver monitoring are recommended, and the risk of hepatotoxicity is higher in the postpartum period.
Yes, breastfeeding is generally considered compatible with isoniazid. Small amounts pass into milk; both mother and infant are often given pyridoxine, and the infant should be monitored by a pediatrician.
Pre-existing liver disease raises the risk of hepatotoxicity, so careful risk–benefit assessment, baseline and periodic liver tests, and strict alcohol avoidance are essential. Dose adjustments or alternative regimens may be considered.
You usually do not stop isoniazid for surgery, but inform your surgical and anesthesia team. They will monitor liver function and review potential drug interactions in the perioperative period.
Isoniazid is effective and commonly used for TB prevention and treatment in people with HIV. Your clinician will check for interactions and ensure appropriate pyridoxine supplementation and monitoring.
Isoniazid can increase blood levels of these drugs, raising side-effect risk. Your clinician may adjust doses and monitor drug levels and symptoms closely.
Yes, but they have a higher neuropathy risk; pyridoxine is recommended. Monitor blood glucose, as illness and medication changes can affect control.
Both are effective; rifampin for 4 months (4R) is shorter and has fewer hepatotoxicity and neuropathy issues, with strong drug–drug interactions due to enzyme induction. Isoniazid for 6–9 months (6H/9H) is preferred when rifampin interactions or intolerance are concerns.
Once-weekly isoniazid plus rifapentine for 3 months (3HP) is as effective as longer isoniazid monotherapy and improves completion rates. Rifapentine has rifamycin-like interactions, so 3HP may not suit patients on interacting drugs.
Both are core first-line drugs, but pyrazinamide is mainly used in the initial intensive phase to shorten total treatment duration. Pyrazinamide more often causes hyperuricemia and gout flares, while isoniazid is more associated with neuropathy.
Isoniazid is bactericidal against rapidly dividing TB and is a backbone of therapy; ethambutol is bacteriostatic and protects against resistance while susceptibilities are pending. Ethambutol can cause optic neuritis and requires vision monitoring; isoniazid’s hallmark risks are hepatotoxicity and neuropathy.
Rifabutin is used instead of rifampin when strong enzyme induction would compromise antiretrovirals or other critical drugs. Isoniazid remains essential unless resistance or intolerance warrants alternative regimens.
Rifampin has far more interactions due to potent CYP and P-glycoprotein induction, lowering levels of many drugs (e.g., warfarin, DOACs, hormonal contraceptives, certain HIV meds). Isoniazid is a CYP inhibitor that can raise levels of specific drugs like phenytoin and warfarin.
Fluoroquinolones are not first-line for latent TB and are generally reserved for contacts of multidrug-resistant TB or intolerance to standard regimens. Isoniazid remains a standard option when susceptibility and tolerance allow.
Ethionamide has a similar target (mycolic acid synthesis) but is used mainly for drug-resistant TB due to poorer tolerability. It causes more GI upset, weight loss, and hypothyroidism; cross-resistance can occur with certain inhA mutations.
Streptomycin is an injectable aminoglycoside now used infrequently because of ototoxicity and nephrotoxicity and the availability of safer oral options. Isoniazid remains a core oral first-line agent for susceptible TB.
Linezolid is reserved for drug-resistant TB or intolerance to first-line agents due to toxicity risks like myelosuppression, optic neuropathy, and serotonin syndrome. Isoniazid is preferred when the strain is susceptible and the patient can tolerate it.
Bedaquiline targets mycobacterial ATP synthase and is used in multidrug-resistant TB regimens, with monitoring for QT prolongation. Isoniazid is for drug-susceptible TB and latent infection; it is not effective when high-level INH resistance is present.
Three months of daily isoniazid plus rifampin (3HR) shortens therapy with similar efficacy and better completion than 6–9 months of isoniazid alone, but adds rifampin’s interaction profile. Choice depends on drug interactions, tolerance, and patient preference.