Bioflo

Quick links to important sections

Bioflo

Treatment option:

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.

Overview of Bioflo

This section provides a factual definition of the medicine Bioflo by detailing its composition, classification, and general purpose, strictly avoiding any discussion of dosages, administration schemes, side effects, or specific diseases it treats.

Property Description
Active Ingredient Ofloxacin
Pharmacological Class Antibiotic (Second-Generation Fluoroquinolone)
Origin Synthetic
Forms Tablets, Ophthalmic solution, Otic solution
Action Type Bactericidal (Kills bacteria)

Bioflo: Definition and Pharmacological Classification

Bioflo is a commercial presentation of the active substance Ofloxacin, which is a synthetic antimicrobial compound. Ofloxacin is classified as an antibiotic and belongs to the second-generation fluoroquinolone pharmacological group. This class is noted for its powerful and rapid bactericidal action against susceptible microbes. This compound’s efficacy is clinically recognized across a broad-spectrum of bacteria.

The essential purpose of this medicine is to stop the progression of an infection by directly destroying the responsible microorganisms.

Composition and Available Pharmaceutical Forms

The medicine is manufactured as a single-entity product, meaning its therapeutic effect stems solely from the Ofloxacin active ingredient. Bioflo is prepared in multiple dosage forms to facilitate targeted delivery. These include tablets for oral ingestion, which provide systemic treatment throughout the body. Additionally, specialized liquid preparations—the ophthalmic solution (eye drops) and otic solution (ear drops)—are formulated with an aqueous vehicle for precise topical/local administration.

The availability of distinct forms ensures the Ofloxacin component can be delivered directly to the required site of action, whether internal or external.

What is the General Therapeutic Purpose of Bioflo?

The overarching purpose of Bioflo as an anti-infective is to achieve the elimination of bacterial threats. The bactericidal mechanism of Ofloxacin actively kills the invading microbes by interfering with the essential bacterial enzymes required for their DNA replication and repair.

The primary general benefit is the elimination of the microbial cause of illness, resulting in the natural resolution of the underlying condition caused by the susceptible bacteria.

What side effects are possible with Bioflo?

Possible Side Effects and Safety Information

The safety profile of Bioflo (Ofloxacin) is formally documented in government regulatory materials, classifying adverse reactions by frequency and the body system affected. This documentation distinguishes between common, generally non-serious events and rare, serious adverse reactions.


Official Adverse Reaction Classification

Adverse effects are categorized based on their documented incidence in clinical studies and post-market surveillance:

  • Common Reactions (may affect up to 1 in 10 people): Nausea, headache, dizziness, insomnia (trouble sleeping), and diarrhea.
  • Uncommon Reactions (may affect up to 1 in 100 people): Vomiting, stomach pain, constipation, dry mouth, gas, and general skin rash.

System-Organ Classes and Serious Adverse Reactions

The label documents effects across several systems, including Gastrointestinal, Nervous System, Psychiatric, and Musculoskeletal disorders. Regulatory documents specifically highlight a class of serious adverse reactions, which, while rare, can be potentially disabling or irreversible.

These serious documented risks include Tendon Rupture, which may occur swiftly (within 48 hours) or be delayed (up to several months after stopping treatment). Other serious documented concerns include disabling effects on the nerves (peripheral neuropathy), aortic aneurysm and dissection, and severe skin reactions.


Population-Specific Safety Considerations

Official prescribing information includes constraints for specific patient groups. Older adults (over 60) have a formally documented increased risk of tendon and aortic complications. Use is generally constrained in the pediatric population due to documented concerns regarding joint cartilage development. Additionally, Ofloxacin is contraindicated in individuals with a history of epilepsy or certain CNS disorders, or prior tendon issues related to fluoroquinolone use.

Overdose and Emergency Response

The official regulatory profile for Ofloxacin (Bioflo) documents specific clinical manifestations associated with overdosage. These presentations include drowsiness, confusion, dizziness, nausea, slurred speech, and localized effects like hot and cold flushes. Overexposure is classified as severe when it affects the Central Nervous System, with potential progression to convulsions (seizures) or toxic psychosis. Documented life-threatening outcomes include ECG QT interval prolongation, which carries a risk of serious ventricular arrhythmias, and the documented possibility of aortic aneurysm or dissection. No specific antidote is known for Ofloxacin overdose, establishing the mandatory need for symptomatic and supportive treatment. This includes ECG monitoring due to the officially noted cardiac risks. Regulators explicitly state that a patient must seek immediate medical attention for critical symptoms such as seizures, new heart palpitations, acute dyspnoea, or sudden severe pain in the chest or back. Patients with renal impairment are noted to be at a heightened risk for accumulation and subsequent neurotoxicity due to slower clearance. The medicine must be discontinued immediately upon the first sign of a severe reaction.

Therapeutic Uses of Bioflo

What Bioflo Treats: Main Uses and Benefits

Bioflo is used for managing a wide range of bacterial infections. Its core therapeutic benefit is to address the underlying cause of illness, which generally helps with managing symptoms that create noticeable physiological strain and localized discomfort.

Key Therapeutic Domains

This medicine is commonly used across conditions characterized by periods of heightened symptoms in several areas: the urinary tract (like infections that affect the upper urinary tract and chronic prostatitis), the respiratory system (such as bacterial pneumonia), and various skin and soft tissue infections (like cellulitis). It is also considered relevant for infections in the pelvic region (e.g., PID and certain STIs) and for local use in the eyes (conjunctivitis, corneal ulcers) and ears (Otitis Externa).

Its application contributes to improved day-to-day comfort during periods of acute inflammation. The medicine contributes to easing the overall symptom load and helps maintain a sense of stability when symptoms are more noticeable.

The therapeutic benefit helps ease the overall symptom burden, particularly in acute episodes of systemic or localized bacterial disease.


Contextual Note: Symptom Management Focus

Contextual Note: Symptom Management Focus Bioflo is applied in clinical settings marked by increased discomfort or tension, providing supportive relief that helps ease symptoms related to physical discomfort (like pain during urination or earache) and symptoms related to systemic imbalance (like fever and chills) that often accompany these bacterial infections.

Regulatory References

  1. NIH National Center for Biotechnology Information Overview

Eligibility and Restrictions for Use

Who can and cannot use Bioflo?

This section defines the official eligibility rules for Bioflo (Ofloxacin) based on government regulatory labeling. The medicine is contraindicated (must not be used) in certain groups to prevent serious, officially documented risks.

Absolute Contraindications

The systemic form (tablets) is contraindicated for patients with a known hypersensitivity to Ofloxacin or any other fluoroquinolone antibiotic. It is also prohibited for patients with a history of tendon disorders related to prior fluoroquinolone use and for those with a history of epilepsy or other CNS disorders that may lower the seizure threshold.

Age-Related Eligibility

Systemic use is contraindicated in children and growing adolescents (typically under 18 years of age). In contrast, the topical forms (eye/ear drops) are approved for use in specific pediatric populations, such as children aged 1 year and older for ophthalmic use.

Conditional Use and Restrictions

Use is restricted or requires caution in several adult populations:

  • Impaired Renal Function: Patients with reduced kidney function (creatinine clearance le 50 mL/min) require close monitoring and often an adjustment to the dose due to reduced clearance.
  • Older Adults: Patients typically ge 60 years of age have an increased risk of tendinitis and tendon rupture and require caution, especially if taking concurrent corticosteroids.
  • Pregnancy and Lactation: Systemic use is generally not recommended by many authorities, and some consider it contraindicated, due to theoretical risks to the fetus or infant.

What should I know about interactions with other medicines?

Bioflo Interactions with other medicines and products

Bioflo's official interaction profile is structured around two primary mechanisms: its role as a potent CYP2D6 enzyme inhibitor and its serotonergic activity. These factors necessitate specific prescribing restrictions and cautions when combining it with other medicinal products.

Contraindicated Combinations

Co-administration of Bioflo with Monoamine Oxidase Inhibitors (MAOIs) is contraindicated, and a mandatory 14-day washout period is required when switching between either drug. The combination of Bioflo with thioridazine or pimozide is also contraindicated. This restriction is due to Bioflo's inhibition of CYP2D6, which significantly increases the plasma concentration of thioridazine and pimozide, raising the risk of QT interval prolongation.

Use-with-Caution Combinations

Caution is required with other serotonergic agents, including Triptans, due to the potential for Serotonin Syndrome. Concomitant use with drugs that increase bleeding risk, such as NSAIDs and anticoagulants like warfarin, requires increased monitoring for abnormal bleeding events. Bioflo's inhibition of CYP2D6 also affects drugs metabolized by this enzyme; specifically, the co-administration with tamoxifen is not recommended as Bioflo may reduce the formation of tamoxifen's active metabolite.

Mechanism of Action

Dual-Targeted Inhibition of Microbial DNA Synthesis

Bioflo operates through two distinct, simultaneous mechanisms to target microbial genetic integrity. The Ofloxacin component acts as an inhibitor of bacterial enzymes DNA gyrase and topoisomerase IV. Binding to and stabilizing the DNA-enzyme cleavage complex, Ofloxacin traps the DNA in a broken state, preventing religation during replication and transcription. Concurrently, the Ornidazole component is selectively reduced in anaerobic organisms, generating highly reactive cytotoxic radicals. These radicals directly interact with and damage the microbial DNA helix.

Mechanistic Cascade of Pathogen Elimination

These actions initiate a mechanistic cascade of overwhelming cellular damage that exceeds the pathogen's repair capacity. The core physiological effect is a bactericidal and protozoacidal action, leading to the non-reversible inhibition of microbial proliferation and viability. This dual action influences the local microbial flora by eliminating microorganisms from two distinct classes: aerobic/facultative bacteria and obligate anaerobes/protozoa.

Dosage and Administration Information

Administration Instructions for Bioflo (Oral Tablet)

This section outlines the guidelines for the administration of the oral tablet formulation of Bioflo.

Administration Scope

Category Administration Guidelines
Route of Administration Oral tablet, swallowed whole with water. Do not crush or chew.
Dosing Schedule A daily dose must be taken as prescribed by a healthcare provider. The exact dosage and duration are determined by the treating physician based on the specific condition.
Timing in Relation to Meals May be taken with or without food.
Preparation Requirements None beyond swallowing the tablet whole.
Age-Group Rules Use is not recommended in children or adolescents. Elderly patients (over 70 years) should be administered the medicine under close medical supervision.
Missed-Dose Instructions If a regular dose is missed, take it as soon as remembered. If it is nearly time for the next scheduled dose, skip the missed one and continue the regular schedule. Do not double the dose.
Special Procedural Conditions It is essential to complete the full course of medication as prescribed, even if symptoms improve earlier. The dosage must never be altered or stopped without consulting a doctor. It is recommended to take the tablet at evenly spaced intervals, preferably at the same time each day.

Connection to the Overall Use Protocol

Bioflo is an antibacterial agent with a specific administration protocol focused on patient adherence and daily regularity. The procedure is a simple oral intake, with flexibility regarding meals, but includes strict rules against prematurely stopping or self-adjusting the prescribed dose, which is intended to prevent treatment failure and bacterial resistance. The regimen emphasizes completing the duration of therapy as outlined by the healthcare provider to ensure effectiveness, with additional caution noted for pediatric and elderly populations.

Recent Clinical Evidence

Research evidence / Overview of studies for Bioflo


Evidence for Use in Urinary Tract Infections (UTIs)

Research examined Bioflo in the context of bacterial infections of the urinary tract (UTIs), including both cases that are uncomplicated and those presenting with structural or functional complexities. Research primarily involved Randomized Controlled Trials (RCTs) and comparative studies, which were used in research exploring how symptoms change over time compared to other established treatments. The studies included populations of adults, including elderly individuals and those with complicated infections.

The trials monitored high-level outcomes related to systemic or functional imbalance, such as whether a change was observed in urine cultures (bacteriological status). Researchers also examined patient-reported outcomes describing perceived discomfort and the change in common UTI symptoms like pain or frequency. Findings describe patterns observed in the studies where clinical and laboratory measurements were monitored following a short course of treatment.

However, the evidence is not uniform. The criteria used to define a "complicated UTI" varied across studies, particularly in older systematic reviews, meaning evidence quality varies across studies. While short-term assessments were frequently reported at the end of therapy, long-term effects are not fully established, and there is limited information for long-term outcomes regarding the risk of a relapse or reinfection after a few weeks.


Evidence for Use in Respiratory and Skin Infections

Research explored settings addressing infections in the respiratory system, such as bacterial pneumonia, and in skin and soft tissues (SSTIs). For respiratory issues, the evidence often draws from multicenter clinical trials that research examined patient groups receiving Bioflo or other antimicrobial agents. These studies explored outcomes reflecting daily functioning or activity level and the microbiological status of the responsible microorganism. For SSTIs, Randomized Comparative Trials research examined clinical signs of infection, such as reductions in redness or swelling, in adults with localized infections.

The research for respiratory infections often relies on data derived from the entire fluoroquinolone class of antibiotics, meaning direct evidence specifically on Bioflo (Ofloxacin) for severe cases is limited. Additionally, most SSTI studies focused on mild to moderate infections, so data for certain groups remain insufficient, particularly concerning deep or complex infections. Comparative evidence is lacking for Bioflo against some of the newest treatment options currently available.


Evidence for Use in Localized Eye and Ear Infections

The available research for the ophthalmic (eye drops) and otic (ear drops) solution forms primarily consists of Clinical Trials focused on topical administration. These studies research examined localized infections, such as bacterial conjunctivitis or external ear infections. The primary focus of these trials was studied for short-term markers of change, rather than systemic effects. Studies described the observed rate of change in localized symptoms within the defined short treatment period. Trials described the patterns of microbiological status in local cultures taken after the short course of topical treatment.

Because the focus is entirely on topical use, the results apply only to the populations studied in this manner. The studies contribute to understanding symptom patterns in acute, localized infections, but they do not determine or provide information regarding effects elsewhere in the body or in chronic, recurring conditions.


\u200d Evidence in Specific Patient Groups and Populations

The majority of the evidence was evaluated in general adult populations. However, some specific patient groups were included in the research base. Adults of older age was studied for UTIs, and data was observed in this group. Nevertheless, subgroup findings are uncertain or limited for populations like pregnant individuals, those who are breastfeeding, or patients with multiple specific, complex underlying diseases. Data for certain groups remain insufficient, and research does not determine whether an individual will respond similarly if they have a complex set of comorbid conditions that were excluded from the main trials.

Key Studies & References

  1. Public Assessment Report Scientific discussion Ofloxacine Stulln Unit Dose (EMA/MEB - Otic Solution)

Frequently Asked Questions (FAQ)

Common questions about Bioflo (FAQ)

Q: What types of bacterial infections is Bioflo most commonly prescribed for?

A: Regulatory information indicates that Bioflo is approved for the treatment of certain infections caused by susceptible bacteria. These commonly include infections of the urinary tract, prostate, respiratory system (like certain types of pneumonia), and skin.

Q: Is Bioflo effective for infections in the urinary tract?

A: Regulatory documents indicate that Bioflo is approved for treating both complicated and uncomplicated urinary tract infections (UTIs). This indication reflects the drug’s established activity against many of the organisms that typically cause UTIs.

Q: Can Bioflo be used to treat pneumonia or other respiratory infections?

A: Official labeling indicates that Bioflo is used to treat certain bacterial respiratory infections. This includes community-acquired pneumonia and acute bacterial exacerbation of chronic bronchitis, when caused by susceptible bacteria.

Q: Does Bioflo interact with common pain relievers like ibuprofen or acetaminophen?

A: Regulatory information advises caution when taking Bioflo with nonsteroidal anti-inflammatory drugs (NSAIDs), such as ibuprofen, due to a possible increased risk of bleeding. Regulatory warnings specifically highlight the need for caution with NSAIDs, but the product label does not typically include a specific caution regarding acetaminophen.

Q: Why is Bioflo classified as 'unsafe' during pregnancy or while breastfeeding?

A: Systemic use of Bioflo during pregnancy is generally not recommended due to theoretical risks to the developing fetus. Regulatory information suggests that for breastfeeding individuals, there is information indicating a potential risk to the infant, such as affecting their normal gut bacteria (gut flora).

Q: Can Bioflo be used for skin and soft tissue infections?

A: Yes, regulatory documents indicate that Bioflo is approved for the treatment of certain skin and soft tissue infections (SSTIs). Its effectiveness depends on the infection being caused by a susceptible type of bacteria.

Q: Can Bioflo cause changes in vision or balance?

A: Official labeling states that Bioflo is associated with central nervous system (CNS) effects. These can include vision problems, such as blurred vision, and general issues like dizziness, and in rare instances, vertigo (a sensation of spinning).

Q: What happens if I take Bioflo with dairy products like milk or cheese?

A: Official regulatory information advises against taking Bioflo at the same time as products containing minerals, including calcium found in dairy. Taking them simultaneously may interfere with the proper absorption of the antibiotic, potentially reducing its effectiveness. Official guidance often recommends separating the administration of the medicine and these products by several hours.

Q: What are the signs of a serious allergic reaction to Bioflo?

A: Serious allergic reactions are rare, but symptoms may indicate a medical emergency. Official warnings state that signs may include hives, difficulty breathing, or swelling of the face, tongue, or throat. Severe skin reactions are also documented as a possible serious risk.

Q: Are there any specific supplements or vitamins that should be avoided while taking Bioflo?

A: Supplements that contain metal ions like calcium, iron, magnesium, or zinc should be separated from your dose of Bioflo by several hours. Taking them simultaneously can bind to the antibiotic, potentially preventing it from being fully absorbed and working properly.

Q: Is Bioflo generally safe for people who have kidney issues?

A: Regulatory documents indicate that patients with reduced kidney function (renal impairment) must use Bioflo with caution. In these cases, dose adjustments may be necessary, based on a healthcare provider's assessment, to prevent the medicine from accumulating in the system.

Q: What should be avoided while taking Bioflo to reduce the risk of side effects?

A: To reduce the risk of phototoxicity (an exaggerated sunburn reaction), official precautions advise avoiding excessive exposure to direct sunlight and artificial UV light. It is also officially recommended that patients exercise caution when driving or operating machinery until they are aware of how the medicine affects them, as it may cause dizziness.

Q: Does taking Bioflo increase sensitivity to the sun or cause photosensitivity?

A: Yes, official warnings state that Bioflo can cause photosensitivity or phototoxicity reactions. This means that exposure to sunlight or artificial UV light can cause the skin to react severely, similar to a bad sunburn.

Q: Is Bioflo the same as Ofloxacin, or is it a combination drug?

A: According to the official description, Bioflo (Ofloxacin) is a single-entity product. This means the therapeutic effect comes solely from the active ingredient Ofloxacin, and it is not a combination drug with other antimicrobial agents.

Q: How long does Bioflo typically stay in your system after the last dose?

A: Regulatory information on the drug’s pharmacokinetics indicates that Ofloxacin is largely eliminated from the body via the kidneys. Most of the administered dose (between 65% and 80%) is typically cleared from the system within 48 hours of taking the last dose.

Q: Is Bioflo used to treat sexually transmitted infections like gonorrhea?

A: Yes, regulatory documents indicate that Bioflo is approved for the treatment of certain sexually transmitted infections. This includes uncomplicated urethral and cervical gonorrhea caused by susceptible organisms.

Q: Does Bioflo have a known effect on the normal bacteria (flora) in the gut?

A: As an antibiotic, Bioflo can affect the natural balance of normal bacteria (flora) in the gut, which can lead to common side effects like diarrhea. In rare cases, this imbalance can lead to a more severe gut infection called C. difficile-associated diarrhea (CDAD).

Q: What should I do if I experience severe or bloody diarrhea while on Bioflo?

A: Official warnings state that if you experience severe abdominal pain, or diarrhea that is watery or bloody, contacting a healthcare provider immediately is advised. This may be a sign of a new, serious infection (C. difficile-associated diarrhea) that requires prompt evaluation.

Q: Is Bioflo known to affect blood sugar levels?

A: Yes, regulatory warnings note that Bioflo has been associated with disturbances in blood glucose. This means it can potentially cause both hypoglycemia (low blood sugar) and hyperglycemia (high blood sugar).

Q: Does Bioflo carry a risk of nervous system side effects like confusion or tremors?

A: Yes, official precautions note that Bioflo is associated with central nervous system stimulation. This can potentially manifest as side effects such as tremors, confusion, agitation, or, rarely, toxic psychosis.

Q: Does Bioflo cause vaginal irritation or yeast infections in women?

A: Post-marketing safety data included in regulatory documents mentions the occurrence of vaginal candidiasis (commonly known as a yeast infection). This is a known risk with antibiotics due to their effect on the body's natural balance of microorganisms.

Q: Can Bioflo be used to treat infections that affect the ears or eyes?

A: Yes, Bioflo (Ofloxacin) is available in specialized topical forms. There are ophthalmic solutions (eye drops) and otic solutions (ear drops) specifically formulated for the local treatment of certain bacterial infections in the eyes and ears.

Q: Is there any research on Bioflo's effectiveness against drug-resistant bacteria?

A: The microbiology section of the official label indicates that the drug may be active against certain bacteria that are resistant to other classes of antibiotics. However, it also notes that some strains of certain microorganisms may develop resistance during the course of treatment.

Q: How does the mechanism of action of Bioflo prevent bacterial cells from dividing?

A: The active ingredient, Ofloxacin, works by inhibiting key bacterial enzymes called DNA gyrase and topoisomerase IV. These enzymes are essential for the bacteria's DNA to replicate, repair, and unwind, meaning their inhibition effectively prevents the bacterial cell from successfully dividing and multiplying.

How should Bioflo be stored and disposed of?

Official Storage and Disposal Requirements for Bioflo

The storage of Bioflo (Ofloxacin tablets) must strictly follow official regulatory instructions to maintain product stability and ensure public safety.

Condition Regulatory Requirement
Storage Temperature Store at room temperature, typically 20 C to 25 C. Do not store above 30 C [WHO; FDA].
Environmental Control The medicine must be kept away from excessive heat, moisture, and direct light. It is required to keep from freezing [NIH MedlinePlus].
Child Safety Keep Bioflo out of the reach and sight of children [NIH MedlinePlus].
Disposal Do not keep outdated or unneeded medicine. Ask a healthcare professional how to dispose of unused product according to local regulations; do not dispose of the product into drains or wastewater [NIH MedlinePlus; Regulatory Safety Data].

These instructions define the mandatory environmental and handling profile, ensuring the antibiotic's stability until its expiration date and preventing environmental contamination upon disposal.

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

Equivalent of Bioflo found in:

A-Z Index: