Keflexin

Quick links to important sections

Medically reviewed

Marina Burgos

Last updated on 10/01/2026

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 Keflexin

Property Description
Active Ingredient Cephalexin
Forms Capsules, Tablets, Oral suspension
Pharmacological Class First-generation cephalosporin
Common Use Treating bacterial infections
Origin Semi-synthetic

What Type of Antibiotic is Keflexin?

Keflexin is a medication containing the active ingredient Cephalexin, which is classified as a semi-synthetic beta-lactam antibiotic. This compound is designated as a first-generation cephalosporin, positioning it within an established class of antimicrobial agents widely utilized in human medicine. Cephalexin is defined as a bactericidal agent, meaning its function is to actively kill susceptible bacteria rather than simply inhibiting their growth. This classification is clinically recognized for effectively targeting common bacterial pathogens, and Cephalexin is a well-established treatment for various infections.


Composition and Forms of Cephalexin

As a single-ingredient product, the core constituent is Cephalexin monohydrate, manufactured for oral administration and systemic delivery throughout the body. The medication is commonly supplied in several forms, including solid capsules and tablets, as well as a powder for oral suspension that is mixed with water to create a liquid. This variety ensures flexibility for different patient populations, including children and those who may have difficulty swallowing solid doses. The drug achieves systemic levels rapidly after oral intake.


The General Principle of How Keflexin Works

Cephalexin's efficacy is based on the inhibition of bacterial cell wall synthesis. The drug achieves this by interfering with the construction and cross-linking of peptidoglycan, a structure essential for the bacterial cell wall's stability. By compromising this structure, the medication causes the wall to fail, leading to the destruction of the bacterial organism. This targeted action is the means by which Cephalexin fulfills its overall benefit of helping the body resolve the underlying bacterial proliferation, such as those involved in typical skin or respiratory tract infections.

What side effects are possible with Keflexin?

Possible Side Effects and Safety Information

The safety profile of Keflexin (Cephalexin) is based strictly on documentation from government regulatory bodies such as the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA). This information outlines officially documented adverse reactions and specific safety constraints for the medication.

Officially Documented Adverse Reactions

Adverse reactions are classified by frequency and body system:

System-Organ Class (SOC) Common Reactions Rare & Serious Reactions
Gastrointestinal Disorders Diarrhea, Nausea Pseudomembranous Colitis (CDAD)
Immune & Skin Disorders Rash, Pruritus Anaphylaxis, Stevens-Johnson Syndrome (SJS), Angioedema
Blood Disorders Eosinophilia (Uncommon) Thrombocytopenia, Leukopenia (Uncommon)
Renal Disorders Interstitial Nephritis

Serious Safety Considerations

The regulatory label explicitly documents serious and clinically significant adverse reactions. These include Anaphylaxis (a severe allergic reaction), Pseudomembranous Colitis (Clostridium difficile-associated diarrhea or CDAD), and severe, rare skin conditions such as Toxic Epidermal Necrolysis (TEN). Furthermore, the official documents list Reversible Interstitial Nephritis as a serious renal disorder.

Population and Exposure Constraints

The official prescribing information notes specific safety restrictions. Caution is required for individuals with a known history of Penicillin Hypersensitivity due to the possibility of cross-allergenicity with cephalosporins. For patients with severely impaired renal function, a dosage adjustment is required because the body's elimination of the drug is reduced. The label also specifies that prolonged use of this antibiotic may lead to the overgrowth of non-susceptible organisms (superinfection).

Overdose and Emergency Response

Overdose and When to Seek Help

The regulatory description of Cephalexin (Keflexin) overdose focuses on specific clinical manifestations and mandated emergency actions. Overdose may present with documented gastrointestinal symptoms, including nausea, vomiting, diarrhea, and epigastric distress. A notable finding reported in official documentation, particularly following high accidental ingestion in children, is hematuria (blood in the urine).

A serious outcome cited in official labeling is the potential for seizures and other signs of neurotoxicity or encephalopathy. This risk is significantly heightened in individuals with impaired renal function if the cephalexin dosage is not appropriately reduced for their condition.

In the event of a suspected overdose, regulatory guidance mandates that immediate medical attention must be sought. Individuals are instructed to immediately contact a healthcare professional, a hospital emergency department, or a regional poison control centre. Regulators state that no specific antidote is known, and the required approach is the institution of general supportive measures. Urgent medical services must be called immediately if the affected person has collapsed, had a seizure, has trouble breathing, or cannot be awakened.

Therapeutic Uses of Keflexin

Quick Facts: Primary Therapeutic Domains

  • Respiratory Infections: May be used to address specific bacterial infections of the respiratory tract.
  • Skin and Tissue: Appropriate for certain bacterial infections affecting the skin and associated structures.
  • Ear Infections: Considered for the management of otitis media caused by susceptible bacteria.
  • Genitourinary Tract: Used in the treatment of specific infections of the urinary and reproductive systems.
  • Bone Health: May be prescribed for certain bacterial infections in the bone.

What Keflexin Treats: Main Uses and Benefits

Keflexin (Cephalexin) is a widely utilized medication applied to address a range of bacterial infections in patients. It is indicated for treatment only when the condition is caused by bacteria proven or strongly suspected to be susceptible to the medication. This therapy is commonly prescribed for several distinct types of infection.

The medication may be an appropriate therapeutic choice for certain bacterial infections of the skin and skin structure. It is also used in the management of middle ear infections, known as otitis media, when caused by susceptible bacteria. Additionally, Keflexin can be administered to address specific infections affecting the bone and the genitourinary tract, which includes the bladder and associated structures. Its applications also extend to certain bacterial respiratory tract infections.

Before initiating any antibacterial therapy, a healthcare provider determines if the treatment is appropriate for the condition. Accessing detailed information regarding the approved indications and usage for this medication is essential for proper administration and management.

Eligibility and Restrictions for Use

The use of Keflexin is strictly governed by its official regulatory status, defining specific populations who must avoid the medicine and others who require special caution.

Eligibility Constraints

Classification Population/Condition
Contraindicated Patients with a known allergy or hypersensitivity to cephalexin or any other member of the cephalosporin class of antibacterial drugs.
Special Caution Individuals with a history of penicillin allergy due to the risk of cross-hypersensitivity among beta-lactam antibiotics.
Restricted Use Patients with markedly impaired renal function (kidney disease); dosage adjustment is necessary to prevent accumulation and potential neurotoxicity/seizures.
Caution Those with a history of gastrointestinal disease, particularly colitis, due to the risk of Clostridium difficile-associated diarrhea (CDAD).
Age-Related Pediatric use is established for children over 1 year of age. Geriatric patients require careful dose selection due to the higher likelihood of decreased renal function.
Physiological State Pregnant women should use the medicine only if clearly needed. Nursing mothers must exercise caution as the drug is excreted in human milk.

All use must be reserved for the treatment of proven or strongly suspected bacterial infections to minimize the development of drug-resistant bacteria, as stated in regulatory guidelines.

What should I know about interactions with other medicines?

Interactions with other medicines and products

The regulatory profile for Keflexin (Cephalexin) is characterized by documented pharmacokinetic interactions involving both renal clearance and gastrointestinal absorption, as well as specific pharmacodynamic risks.

Drug-Drug and Drug-Substance Interactions

Co-administration with Probenecid is not recommended because the latter substance inhibits the renal tubular secretion of Cephalexin, which formally increases the antibiotic’s systemic exposure and plasma concentrations. Cephalexin also interacts by increasing the exposure ( Cmax and AUC) of the oral antidiabetic medicine Metformin due to a reduction in its renal clearance.

A specific pharmacodynamic risk is associated with co-administration of anticoagulants (e.g., Warfarin), which may result in an increased risk of bleeding due to a potential fall in prothrombin activity.

Administration Constraints

To prevent a significant reduction in drug absorption, co-administration with zinc-containing products must be separated by a minimum of 3 hours. The regulatory documentation states that while food may delay absorption, the total amount absorbed is not appreciably altered, permitting administration without regard to meals. Furthermore, co-administration with other nephrotoxic drugs may enhance the risk of nephrotoxicity, particularly in patients with impaired kidney function.

Drug-Laboratory Test Interactions

Cephalexin can cause a false-positive reaction for glucose in the urine when tested with solutions like Benedict’s, Fehling’s, or Clinitest® tablets.

Mechanism of Action

Keflexin's action is strictly defined by its role as an irreversible enzyme inhibitor within the bacterial cell wall synthesis pathway. The drug functions by gaining access to susceptible bacterial cells, where it selectively targets and binds to Penicillin-Binding Proteins (PBPs). These PBPs are critical bacterial transpeptidases responsible for the final stage of peptidoglycan cross-linking. Keflexin, a beta-lactam molecule, structurally mimics the D-Ala-D-Ala terminus of the peptidoglycan precursor, which allows it to covalently acylate the active site of the PBP. This irreversible binding prevents the enzyme from catalyzing the necessary cell wall construction. The resulting lack of proper cell wall formation leads to structural fragility and an inability to withstand internal osmotic pressure. This mechanistic cascade culminates in the activation of bacterial autolytic enzymes and, ultimately, the rapid rupture of the bacterial cell (lysis), neutralizing the susceptible microbe.

Dosage and Administration Information

How Keflexin is Used

Keflexin (Cephalexin) is an antibiotic prescribed strictly for oral administration. The medication is available as capsules, tablets, and a powder that must be reconstituted to create an oral suspension.

General Dosing and Administration

The frequency and total duration of use are established through clinical protocols.

Administration Scope Standard Dosing Protocol
Standard Adult Dose Typically 250 mg every 6 hours (q6hr) or 500 mg every 12 hours (q12hr).
Maximum Daily Dose Up to 4 grams in equally divided doses for severe infections.
Timing Relative to Meals May be taken without regard to meals (with or without food).
Course Duration Ranges from 7 to 14 days; a minimum of 10 days is required for beta-hemolytic streptococcal infections.

Population-Specific Adjustments

Specific dosage modifications are required for certain patient groups to ensure proper use:

  • Pediatric Use: Dosing is based on body weight, typically 25 to 50 mg/kg/day in divided doses, or up to 100 mg/kg/day for conditions like otitis media.
  • Renal Impairment: Dosing must be reduced in adults with significantly impaired kidney function (Creatinine Clearance <30 mL/min). In severe impairment, the daily dose may be limited to 500 mg or 1 gram, depending on the severity and specific clinical guidance.

Preparation Instruction

If using the oral suspension form, the medication must be reconstituted with water before the first use and shaken well before each subsequent dose. The total course of treatment must be completed as prescribed, adhering to the specified time intervals (q6hr, q8hr, q12hr).

Recent Clinical Evidence

Research evidence / Overview of studies for Keflexin

Research Evidence for Skin and Soft Tissue Infections

Keflexin was studied in conditions characterized by acute or disruptive episodes affecting the skin and associated soft tissues, such as cellulitis or impetigo. The research exploring short-term symptom changes in this area relies significantly on Randomized Controlled Trials (RCTs) and systematic reviews. These studies primarily monitored outcomes related to physical discomfort and Clinical Outcome, which researchers defined as the resolution of infectious signs like pain or purulent drainage. Microbiological Endpoint, the monitoring of the causative bacteria, was also observed in research.

What remains unclear is the research on appropriate administration for certain infections, such as cellulitis. Additionally, data for certain groups remain insufficient for the evaluation of emerging bacterial resistance patterns. The results apply only to the populations studied, and follow-up durations were limited, typically only tracking outcomes for about one week post-treatment.


Research Evidence for Respiratory and Ear Infections

Research was evaluated in specific settings related to the respiratory tract and for middle ear infections (Otitis Media) in children. The evidence base here is supported largely by reviews of historical clinical experience and Comparative Trials rather than recent, large-scale RCTs for general usage. Studies monitored outcomes related to systemic or functional imbalance, such as the Clinical Response or Outcome of symptoms, and the Bacteriological Cure Rate.

Evidence contributes to understanding symptom patterns, and findings describe patterns observed in studies where the infection was caused by specific, susceptible bacterial strains. However, evidence suggests a limited spectrum of activity against certain common respiratory pathogens like Haemophilus influenzae, meaning this bacterium was observed in some studies.


Follow-up and Long-Term Research

Research exploring short-term symptom changes is the predominant focus of the available clinical evidence. These short follow-up durations were limited and provided insight into immediate clinical and microbiological changes.

Research highlights what is known—that is, the patterns observed during the initial treatment—but long-term effects are not fully established regarding the durability of response or the frequency of infection recurrence (relapse). There is limited information for long-term outcomes that may extend months or years beyond the initial therapy period.

Frequently Asked Questions (FAQ)

Common questions about Keflexin (FAQ)

Q: What is Keflexin used for?

A: Keflexin (cephalexin) is an antibiotic used to treat a variety of bacterial infections. It works by stopping the growth of bacteria. It is commonly prescribed for:

  • Respiratory tract infections (like tonsillitis and pharyngitis)
  • Ear infections (otitis media)
  • Skin and soft tissue infections
  • Bone infections (osteomyelitis)
  • Genitourinary tract infections

It is important to remember that Keflexin only treats infections caused by bacteria and will not work for viral infections like the common cold or flu.

Q: How should I take Keflexin?

A: You should take Keflexin exactly as prescribed by your healthcare provider. The dose and duration of treatment depend on the type and severity of the infection.

  • Keflexin can usually be taken with or without food. Taking it with food may help decrease stomach upset.
  • If you are taking the liquid suspension, shake the bottle well before measuring your dose.
  • Do not skip doses and continue taking this medication for the full time prescribed, even if your symptoms begin to improve before the medication is finished. Stopping early can lead to the return of the infection.

Q: What should I do if I miss a dose of Keflexin?

A: If you miss a dose, take it as soon as you remember. However, if it is almost time for your next scheduled dose, skip the missed dose and continue with your regular dosing schedule. Do not take two doses at the same time to make up for a missed dose.

Q: What are the common side effects of Keflexin?

A: Like most medications, Keflexin can cause side effects. The most common ones are generally mild and may include:

  • Diarrhea
  • Nausea and vomiting
  • Upset stomach
  • Headache
  • Vaginal yeast infection (in women)

If any of these effects persist or worsen, contact your healthcare provider. More serious, but rare, side effects, such as signs of a severe allergic reaction (hives, difficulty breathing, swelling of the face/throat) or severe diarrhea, require immediate medical attention.

Q: Can I drink alcohol while taking Keflexin?

A: It is generally recommended to avoid or limit alcohol consumption while taking Keflexin. While Keflexin is not known to cause a severe reaction when mixed with alcohol like some other antibiotics, alcohol can potentially worsen side effects such as nausea, dizziness, and headache. Alcohol can also interfere with your body's ability to recover from the infection and may prolong your illness.

How should Keflexin be stored and disposed of?

How to Store and Dispose of Keflexin (Cephalexin)

Official regulatory guidelines strictly define the storage and disposal requirements for Keflexin (Cephalexin) based on its form.

Drug Form Required Storage Temperature Stability/Shelf-life
Capsules/Tablets Controlled Room Temperature (20 C to 25 C) Until expiration date
Oral Suspension (Mixed) Refrigerated (2 C to 8 C) Discard after 14 days

All forms must be kept in their tightly closed, original container and protected from excess heat, moisture, and light. The reconstituted oral suspension must not be frozen. For safety, the medication must be stored out of the reach of children and pets. Disposal of unused or expired Keflexin should follow FDA guidelines, preferably utilizing a drug take-back program. If a program is unavailable, mix the medicine with unappealing material, seal it in a bag, and dispose of it in the trash.

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

Available in countries:

Equivalent of Keflexin found in:

A-Z Index: