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5-НОК

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5-НОК

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Medically reviewed

Rosario Oropesa

Last updated on 22/12/2025

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

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Overview of 5-НОК

What is 5-НОК? (Nitroxoline)

Property Description
Active ingredient Nitroxoline (5-nitro-8-hydroxyquinoline)
Form Oral Tablet
Pharmacological class Antibacterial Agent (Uroantiseptic)
General purpose Controlling microbial presence in the urinary tract
Origin Synthetic compound

Defining 5-НОК: Classification and Chemical Origin

The medicine 5-НОК is a pharmaceutical preparation containing the active substance Nitroxoline, known chemically as 5-nitro-8-hydroxyquinoline. Pharmacologically, it is classified as a synthetic Antibacterial Agent for systemic use, specifically designated as a urinary antibacterial agent or uroantiseptic.

Nitroxoline is a synthetic compound, being a derivative of 8-hydroxyquinoline. Its unique chemical structure is essential to its function, enabling the drug to achieve high therapeutic concentrations specifically within the urinary tract system upon being processed by the body. Nitroxoline is an antimicrobial agent primarily targeting uropathogens, providing targeted chemical action against microbes within the urinary system.

Composition, Form, and General Purpose

The 5-НОК drug is supplied as a single-ingredient medicine, typically in the physical form of an oral tablet. The core composition includes only the active component, Nitroxoline, combined with the inert excipients that serve as the solid pharmaceutical vehicle. It is generally intended for the adult patient group.

The overarching purpose of 5-НОК is to address and control the presence of microorganisms, including bacteria and certain fungi, in the urinary system. It functions primarily as a bacteriostatic agent; its main mechanism involves binding to essential metal ions, which prevents microorganisms from synthesizing new genetic material and thereby inhibits their growth and reproduction. This action helps halt the proliferation of infection-causing microbes, making it a choice for managing microbial presence in the urinary tract.

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What side effects are possible with 5-НОК?

Possible Side Effects and Safety Information: 5-НОК (Nitroxoline)

5-НОК (Nitroxoline) is generally considered to have a low risk of adverse effects, with most reported reactions being mild and reversible. The safety profile is based on decades of clinical use in various countries.

Adverse Reactions by Frequency

The table below summarizes the most common types of adverse effects associated with 5-НОК, based on clinical data and regulatory documentation:

Classification System-Organ Class Common Reported Adverse Reactions
Common Gastrointestinal System Nausea, vomiting, diarrhea, abdominal pain
Uncommon Skin and Subcutaneous Tissue Disorders Allergic skin reactions (e.g., reddening, itching, rash)
Rare to Very Rare Hematologic/Neurologic Allergic changes to the blood count (e.g., reduction in blood platelets), fatigue, headaches, vertigo, insecurity of gait

Note: The frequency is typically defined as: Common (1 to 10 in 100 persons), Uncommon (1 to 10 in 1,000 persons), Rare (1 to 10 in 10,000 persons), and Very Rare (less than 1 in 10,000 persons).

Other Safety Considerations

  • Urine and Skin Discoloration: A noted effect of the active substance is the temporary yellow coloring of the urine. In rare instances, a slight excretion via sweat may lead to a temporary yellow coloration of the skin, hair, and nails.
  • Serious Adverse Reactions: Severe allergic reactions are possible but rare. Neurological side effects, while rare, may include vertigo and insecurity of gait.
  • Contraindications: 5-НОК is generally contraindicated in cases of severe impairment of renal and hepatic functions. Individuals with known hypersensitivity to the drug's components should avoid its use. The presence of specific inactive ingredients, such as soy oil or certain colorants, may pose a risk for severe allergic reactions in rare cases.
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Overdose and Emergency Response

Overdose and when to seek help

The official regulatory profile for 5-НОК (Nitroxoline) describes a generally low acute toxicity profile in overdose situations. Documented clinical data suggests that specific, severe side effects from ingesting an excessively high dose have not been consistently observed or formally reported in regulatory labeling. The known manifestations of acute massive ingestion are typically non-life-threatening and may include generalized systemic symptoms such as fatigue. Severe complications affecting major organ systems are not officially listed as routine outcomes, confirming a relatively wide therapeutic margin.


Emergency Action and Supportive Management

Immediate action is required based on the severity of the exposure. If the ingested amount is known or suspected to be very high, a doctor or emergency medical services must be consulted immediately for medical evaluation and monitoring. Conversely, in cases of only slight overdose, official regulatory guidance indicates that no specific medical measures are necessary as a rule for resolution.

Overdose management is restricted entirely to symptomatic and supportive treatment appropriate for the patient’s clinical status. This approach is mandated because no specific antidote is known or documented in the official regulatory prescribing information for Nitroxoline overdose. There are no population-specific considerations regarding management or severity detailed in the official overdose sections.

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Therapeutic Uses of 5-НОК

What 5-НОК Treats: Main Uses and Benefits

Targeted Relief for Acute Symptomatic Discomfort

This therapeutic domain covers the management of acute, disruptive symptoms that are often associated with conditions presenting with acute episodes. As a urinary antibacterial agent, its role includes applications in situations involving infections commonly found in the urinary tract. It helps address symptoms related to inflammatory or irritative states that interfere with daily functioning, such as those that may appear suddenly or intensify over time. The treatment generally contributes to improved comfort during periods of heightened symptoms.

Quick Fact: Support for Irritative Symptoms The medicine is associated with scenarios that involve supportive management for acute infectious conditions like cystitis and urethritis, and sometimes mild pyelonephritis.

Supporting Stability in Recurrent Symptom Patterns

It is utilized in conditions involving episodic or fluctuating manifestations that may intensify temporarily, and is applied in contexts where additional symptomatic support is needed. It is applied in addressing conditions that involve acute and recurrent urinary tract infections, and may assist with those following urological procedures, including infections caused by susceptible organisms like certain Candida species. This supports the patient during difficult episodes by easing distress and assists with maintaining functional stability.

“Applied in clinical settings marked by increased discomfort or tension, this treatment may assist with managing symptoms and supports general well-being during symptomatic phases.”

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Eligibility and Restrictions for Use

Who can and cannot use 5-НОК?

The population eligibility for 5-НОК (Nitroxoline) is governed strictly by official regulatory labeling, defining groups who may use the medicine and those who must not.


Official Eligibility Status

Classification Population Group Regulatory Status
Allowed Adult Patients Standard population for use.
Contraindicated Severe Hepatic or Renal Dysfunction Absolute prohibition.
Contraindicated Hypersensitivity Prohibited for known allergy to Nitroxoline or excipients.

Age and Physiological Restrictions

Use is generally limited to adults. The standard dosage form is not intended for children, with lower-dose formulations potentially required for pediatric use.

Pregnancy status is highly conditional: use is only permitted if a compelling indication exists, as the regulatory data cannot rule out a neurotoxic risk to the fetus. Use during lactation is not recommended due to a lack of data on transfer into breast milk and potential risks to the infant's gut flora. Strong renal insufficiency may also limit eligibility by severely reducing the medicine’s clinical effectiveness.

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What should I know about interactions with other medicines?

Interactions with other medicines and products

The official regulatory profile for Nitroxoline (5-НОК) is defined primarily by a required administration-timing constraint to prevent a chemical interaction that impairs drug absorption. This constraint is crucial because Nitroxoline is chemically classified as a metal chelator.


Administration-Timing Interaction Requirements

Category Regulatory Constraint
Interacting Substances Metal-ion containing preparations, including Magnesium supplements, Iron supplements, Tetracycline, Fluorides, Aminoquinolines, Nitrofurantoin, and Bisphosphonates.
Required Separation To prevent the impairment of absorption, Magnesium-containing preparations must be taken 3 to 4 hours before or after the administration of Nitroxoline.

High-Level Interaction Profile

The regulatory documentation mandates a timing-based procedural constraint for co-administration with these metal-ion containing products. This requirement ensures that the drug's exposure is not compromised by chelation in the gut. The official profile is otherwise characterized by a lack of explicit documentation regarding other common interaction types. No formal statements are available concerning interactions mediated by CYP enzymes, drug transporters, or pharmacodynamic effects outside of this essential chelation constraint.

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Mechanism of Action

Targeting Essential Bacterial Enzymes

This drug acts primarily as a non-competitive inhibitor of two critical bacterial enzymes: DNA gyrase (a Type II topoisomerase) and Topoisomerase IV. These enzymes are necessary for managing the complex topology of bacterial DNA, including supercoiling, unwinding, and repair during cell division. The drug binds to the enzyme-DNA complex, interfering with the crucial cutting and re-sealing cycle of the bacterial DNA strand. This molecular interference directly halts the vital process of DNA replication and subsequent cell division, leading to the inactivation or death of susceptible microorganisms.


Chelation and Biofilm Integrity

Additionally, the drug exhibits a chelating property, binding to divalent metal ions (e.g., iron and zinc) that are essential cofactors for numerous bacterial metalloenzymes necessary for metabolism and survival. Sequestering these ions disrupts energy-producing pathways and weakens the structural bonds of the protective biofilm matrix. This combined action increases the microorganism's susceptibility to the drug's primary inhibitory mechanism, resulting in a net reduction in the population of susceptible microorganisms.

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Dosage and Administration Information

How to Use 5-НОК: General Administration Standards

The administration of 5-НОК (Nitroxoline) is structured according to standardized instructions that define the route, frequency, and duration of use. These guidelines establish a consistent approach to the intake of the medicine.


Administration Scope

Entity Instruction
Route of administration The drug is for oral intake only, supplied as a tablet or capsule intended to be swallowed whole.
Dosing schedule The standard total daily dose for treatment in adults typically ranges from 300 mg to 500 mg of Nitroxoline.
Timing in relation to meals Administration is generally instructed to occur about one hour before meals and requires a full glass of water.
Age-group administration rules Pediatric dosing is weight-based, often calculated as 10 mg/kg to 20 mg/kg of body weight per day, distributed into multiple doses.
Missed-dose rules General guidance specifies that if a dose is missed, compensation should not occur by doubling the subsequent dose; the next scheduled dose should be taken as planned.

Resulting Procedural Structure

The standard use pattern requires the total prescribed amount to be divided into a multiple-times-daily schedule, most commonly three times per day. This procedural framework ensures the use aligns with specific time constraints and frequency. The patient must complete the entire prescribed course duration without stopping prematurely.

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Recent Clinical Evidence

Research evidence / Overview of studies for 5-НОК (Nitroxoline)


Evidence for Acute Uncomplicated Urinary Tract Infections (uUTI)

Research examining the use of 5-НОК for conditions associated with acute or disruptive episodes primarily consists of Randomized Controlled Trials (RCTs) and systematic reviews that consolidate the findings of these trials. These studies were generally applied in research exploring how symptoms change over time in populations, mainly adult females, relevant in trials assessing short-term or episodic symptom patterns related to bladder infections. Researchers monitored two main outcomes: microbial presence and clinical efficacy, which explored whether changes occurred in outcomes related to physical discomfort or functional imbalance.

The consolidated research describes patterns observed in these studies, where measurements of microbial presence clearance were reported at specific short-term check-in points, typically within two weeks after the end of the treatment period. The evidence base for this context has been evaluated and is broadly classified as Moderate in consistency, primarily due to the availability of controlled trial data, which contributes to the broader evidence landscape for this condition. Existing studies provide limited information about longer-term outcomes beyond the initial post-treatment check-in.


Research on Supporting Stability in Recurrent Infections (rUTI)

5-НОК was studied for use in research exploring recurrent infection patterns, which are conditions characterized by fluctuating or episodic manifestations. The evidence for this scenario is derived mainly from a combination of older, often uncontrolled clinical studies and subsequent observational settings evaluating daily-life functioning in patients who had experienced multiple prior infections. Research examined outcomes reflecting how often symptoms returned, or the duration of time patients remained symptom-free.

The overall certainty surrounding research on recurrent infections remains low. This is because data for long-term outcomes are still emerging, and there is a limited number of modern, large-scale RCTs that specifically monitored recurrence over extended periods. Comparative evidence is lacking for current long-term strategies, and the reliance on historical data means evidence quality varies across studies.


Key Research Gaps and Uncertainties

The research landscape for 5-НОК includes several important limitations. Firstly, the quality of evidence varies across studies, with modern, high-quality RCT data primarily exploring only the acute, uncomplicated scenario. Secondly, there is a consistent lack of comparative evidence against newer antibiotic treatments for both acute and recurrent infection patterns. Furthermore, long-term effects are not fully established, as follow-up durations were limited in the most reliable studies. Research provides context but not individual predictions, and the evidence highlights what is known about group patterns—but significant questions remain regarding the drug’s role in specific MDR clinical scenarios where research is ongoing.

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Frequently Asked Questions (FAQ)

Common questions about 5-НОК (FAQ)

Q: What is the main difference between 5-НОК and other similar medicines for urinary tract infections?

According to regulatory information, the active ingredient, Nitroxoline, is a unique type of antimicrobial called a hydroxyquinoline derivative. Its mechanism involves two distinct actions: it affects bacterial DNA replication by affecting certain enzymes (gyrases), and it binds to essential metal ions (chelation) that bacteria need. The mechanism of action is distinct from many other antibiotic classes commonly prescribed for UTIs.

Q: Why is 5-НОК sometimes prescribed instead of broad-spectrum antibiotics?

Official information indicates that 5-НОК is active against a wide variety of susceptible Gram-positive, Gram-negative, and fungal pathogens. In certain studies, it is reported to retain activity against some multidrug-resistant strains of E. coli (a common uropathogen). Its profile is studied for use in specific infection patterns.

Q: Are there any specific foods or drinks that should be avoided while using 5-НОК?

Official documents do not list common foods or drinks that must be avoided entirely. The drug’s chelating property requires that it be separated by time (e.g., 3 to 4 hours) from the intake of preparations containing metal ions like magnesium or iron. This timing constraint is required to minimize the risk of compromised absorption.

Q: Is 5-НОК safe to use for men as well as women?

Official product information confirms that 5-НОК is indicated for the treatment and prevention of urinary tract infections in both adults and children. The drug’s use is governed by the specific indication and known contraindications, such as severe liver or kidney problems.

Q: How long is a typical course of treatment with 5-НОК?

The total duration of the course can vary depending on the type and severity of the infection being addressed. Studies often examine a course of 5 days for sporadic, uncomplicated infections. For recurrent or chronic infection patterns, treatment may be extended to 10 days or longer, but the precise duration is based on the prescribed protocol.

Q: Is 5-НОК commonly used for preventing recurrent infections?

Yes, official product information includes the use of 5-НОК for the prevention of recurrent urinary tract infections (rUTI). Regulatory information confirms that the drug is used for this specific indication.

Q: What evidence exists regarding 5-НОК use in children?

Regulatory guidelines provide specific dosing rules for pediatric use, and the drug has been part of clinical practice for acute and recurrent UTIs in children for many years in various countries. Published studies have examined its clinical and bacteriological outcomes in pediatric populations.

Q: Can 5-НОК be used for chronic conditions?

Official regulatory information states that the drug is used for the treatment of acute, chronic, and recurrent urinary tract infections. This scope includes infections that may be long-lasting.

Q: What types of bacteria is 5-НОК primarily designed to treat?

5-НОК is described as being active against a broad range of susceptible microorganisms, including both Gram-positive and Gram-negative bacteria commonly responsible for UTIs, such as E. coli and K. pneumoniae. The active substance also has documented activity against certain fungal pathogens, such as Candida species.

Q: Can I take 5-НОК if I am taking supplements like vitamins or minerals?

The instructions require a separation period of 3 to 4 hours when taking supplements containing metal ions (e.g., Magnesium or Iron). This time constraint is necessary because the drug's chelating nature can significantly reduce its absorption if taken too closely to metal ions. The primary constraint listed relates specifically to metal-ion containing supplements.

Q: Does 5-НОК require a dose adjustment for people with mild kidney problems?

Official product information lists severe renal (kidney) impairment as a clear contraindication. While this clearly restricts use for severe cases, the specific guidance for mild kidney impairment is not typically detailed in general summaries. Guidance on dose adjustment or suitability for mild impairment is determined by the healthcare provider.

Q: How is the action of 5-НОК different from penicillin?

Official sources describe 5-НОК's mechanism as involving the inhibition of bacterial gyrases (key enzymes for DNA) and metal ion chelation. The mechanism differs from penicillin-class drugs, which primarily function by interfering with the construction of the bacterial cell wall.

Q: Are there any drug-drug interactions that are considered particularly serious with 5-НОК?

The official profile mandates a 3-4 hour separation from preparations containing metal ions (like iron or magnesium). This procedural constraint minimizes the risk of the drug's absorption being compromised. The regulatory profile is otherwise largely characterized by a lack of explicit statements regarding other common interaction types.

Q: Do studies suggest 5-НОК works well against drug-resistant bacteria?

Studies suggest that the active substance, Nitroxoline, is reported to demonstrate high in vitro activity against susceptible bacteria. This activity includes some strains of E. coli that have been identified as multidrug-resistant. Regulatory-adjacent evidence indicates that resistance to 5-НОК remains rare.

Q: Is 5-НОК an antibiotic or something else?

The drug 5-НОК is officially classified as an antibacterial agent, which falls under the broader category of anti-infective agents. The active substance is Nitroxoline.

Q: How quickly does 5-НОК typically start to work after the first dose?

While the onset of symptom relief is specific to each person, studies indicate that the active substance, Nitroxoline, is quickly absorbed into the body. It reaches a high, microbiologically active concentration in the urine within approximately 1 hour of oral administration.

Q: Does 5-НОК affect the gut microbiome or 'good bacteria'?

Studies have been published that report treatment with 5-НОК has no significant effect on faecal flora, which are the natural bacteria residing in the gut.

Q: What official body (like FDA or EMA) describes the standard uses for 5-НОК?

The standard uses and regulatory constraints for 5-НОК are established by government health authorities in countries where it is approved. This includes agencies like the European Medicines Agency (EMA), as well as various national health authorities, particularly across Central and Eastern Europe.

Q: What is the active ingredient in 5-НОК?

The active ingredient in the drug 5-НОК is Nitroxoline. Chemically, it is known as 5-nitroquinolin-8-ol.

Q: Is 5-НОК available without a prescription in some countries?

Regulatory information from some international manufacturers indicates that 5-НОК may be available for sale as an Over-The-Counter (OTC) product in certain jurisdictions. However, its status (prescription vs. OTC) depends on the specific country's laws.

Q: If I have a known allergy to other antibiotics, can I still take 5-НОК?

The official safety information specifies that the drug should not be used if a person has a known hypersensitivity to the active substance, Nitroxoline, or to quinolines (a related chemical group). Any potential risk of cross-reactivity with other antibiotic classes should be reviewed with a healthcare professional.

Q: Are there specific storage instructions for 5-НОК?

Official product information suggests the drug should be kept in its original packaging and stored at a temperature not exceeding 25 °C (about 77 °F). Official instructions state that it should be kept out of the reach of children.

Q: Why is 5-НОК sometimes described as a chemotherapeutic agent?

The term chemotherapeutic agent may be used in certain contexts because the mechanism of action, which includes gyrase inhibition and metal chelation, is shared with some non-antibiotic drugs. The active substance has also been the subject of research for potential use as an anticancer and antifungal agent.

Q: How long does 5-НОК stay in the body after the last pill?

The drug is rapidly metabolized in the liver after intake. While the exact total elimination time (half-life) is not usually the focus of patient summaries, the drug reaches its highest concentration in the urine within about 1 to 4 hours and is then largely excreted through the urine.

Q: Is 5-НОК commonly prescribed in all regions of the world?

5-НОК is an older antimicrobial whose use is well-established and widespread in many European and Central/Eastern European countries. However, its use is not common in other regions of the world, such as North America (US/Canada).

Q: Is it true that 5-НОК is an older drug?

Yes, the drug 5-НОК is an established antimicrobial. The active substance, Nitroxoline, was first described in the 1950s and has been in clinical use since the 1960s.

Q: Are there official statements about 5-НОК's ability to prevent resistance development?

While official information notes that resistance to 5-НОК has remained rare and has not significantly evolved in decades, there are no definitive regulatory statements regarding its ability to prevent resistance development. The rarity of resistance may be linked to its unique mechanism.

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How should 5-НОК be stored and disposed of?

The storage and disposal of 5-НОК (Nitroxoline) must strictly follow the official instructions provided on the regulatory label to maintain the drug's quality and ensure safety.

Storage Conditions

Requirement Regulatory Statement
Temperature Store at controlled room temperature, typically below 30 C.
Protection Keep in a dry place and protect from light. The container must be kept tightly closed.
Security Keep out of the sight and reach of children.

Disposal Instructions

Unused or expired 5-НОК must be disposed of according to local regulatory requirements. The official instructions generally advise against flushing the medicine down the toilet or throwing it into wastewater unless specifically listed by a national authority. Proper disposal often involves following local community drug take-back programs.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

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