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Keflin (Cephalexin)

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Keflin (Cephalexin)

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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.

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Overview of Keflin (Cephalexin)

Property Description
Active Ingredient Cephalexin (Monohydrate)
Form Capsules, tablets, oral suspension
Pharmacological Class beta-lactam antibiotic
Common Use Treating bacterial infections
Origin Semi-synthetic derivative

What Type of Medicine is Cephalexin (Keflin)?

Cephalexin is a semi-synthetic beta-lactam antibiotic that functions as a bactericidal agent, classified specifically as a first-generation cephalosporin. This medication is clinically recognized for its reliable efficacy against a range of susceptible bacterial pathogens, making it a well-established compound in antimicrobial therapy. Cephalexin is the International Nonproprietary Name (INN) for the active substance, which was a founding member of this class.

The compound belongs to the broader beta-lactam class, possessing a characteristic chemical structure essential for its action. Its designation as a first-generation cephalosporin positions it within a group that provides effective treatment primarily against common Gram-positive bacteria, offering a foundational therapeutic option within the class of antimicrobial agents.


Composition, Forms, and General Purpose

The pharmaceutical product is a single-entity preparation containing Cephalexin as its sole active ingredient, prepared for oral administration. The active component is often manufactured as Cephalexin monohydrate, and is available in different high-level dosage forms, including solid capsules and tablets, as well as a powder for oral suspension that is mixed into a liquid. The availability of the oral suspension is particularly relevant for individuals, such as the pediatric patient group, who require liquid medications.

The medicine’s general purpose is achieved through its bactericidal mechanism, which involves disrupting the synthesis of the bacterial cell wall. This means the drug actively kills the bacteria responsible for the infection. The final composition includes pharmaceutical excipients—such as binders, fillers, or flavorants—which ensure the product's stability and proper oral delivery.

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What side effects are possible with Keflin (Cephalexin)?

Possible Side Effects and Safety Information

The safety profile of Cephalexin is structured by regulatory documents based on the frequency and the physiological system affected. The most commonly reported adverse reactions involve the Gastrointestinal Disorders system, including diarrhea, nausea, and vomiting. Skin and Subcutaneous Tissue Disorders, such as rash and urticaria, are also commonly documented.


Safety data is organized by System-Organ Class (SOC) to provide a comprehensive overview. Documented effects also occur in the Blood and Lymphatic System (e.g., eosinophilia, neutropenia) and Hepatobiliary Disorders (e.g., transient hepatitis or cholestatic jaundice), though these are classified as uncommon or rare.


Serious Adverse Reactions and Key Constraints

Official labeling explicitly identifies rare but serious adverse reactions. These include severe hypersensitivity events, such as anaphylaxis and severe skin reactions (like Stevens-Johnson Syndrome or Toxic Epidermal Necrolysis). Pseudo-membranous colitis, a severe form of bowel inflammation, has been reported and may occur even after the medicine course is complete.

Safety constraints mandate caution in specific populations. The medicine is contraindicated in individuals with known hypersensitivity to cephalexin or any other cephalosporin. Caution is also required in patients with a history of penicillin allergy due to the documented risk of cross-sensitivity among beta-lactam antibiotics. Furthermore, official documents note that patients with renal impairment require particular caution due to the drug's primary route of excretion, which increases the potential for adverse effects such as neurotoxicity.

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Overdose and Emergency Response

Overdose and When to Seek Help

Official regulatory documentation describes the manifestations of Cephalexin overdose primarily involving the gastrointestinal and central nervous systems. Documented overdose presentations include nausea, vomiting, diarrhea, and epigastric distress. A specific finding reported in children following the ingestion of large amounts (over 3.5 g in a single day) is hematuria (blood in the urine).

Overdose can lead to severe neurological sequelae, including tremor and convulsions (seizures). This risk is particularly noted for patients with impaired renal function, as Cephalexin is substantially excreted by the kidney, and reduced function can lead to increased drug accumulation and toxicity.

Regulatory guidance mandates that individuals seek immediate medical attention and contact a poison control center or emergency room at once if an overdose is suspected. Immediate emergency services (911 or equivalent) must be called if the individual has collapsed, had a seizure, has trouble breathing, or cannot be awakened. No specific antidote is known for Cephalexin overdose; management consists of general supportive and symptomatic treatment. Close clinical and laboratory monitoring is recommended following severe overdosage until the patient is stable.

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Therapeutic Uses of Keflin (Cephalexin)

Cephalexin is commonly used across conditions characterized by periods of heightened symptoms driven by susceptible bacteria. It is applied across several therapeutic domains where supportive symptom management is appropriate. It helps address groups of symptoms that may become intense, which often leads patients to seek relief.

This medication is relevant for managing acute episodes of bacterial infections, including skin and soft tissue infections (such as cellulitis and impetigo), respiratory and ear infections (like strep throat and otitis media), and genitourinary tract infections (such as acute cystitis). In these scenarios, Cephalexin plays a role in managing symptoms related to inflammatory or irritative states.

The main therapeutic benefit is that the medication contributes to easing the overall symptom load in situations involving certain distressing symptoms. This supports the patient during difficult episodes, assisting with maintaining functional stability.

“The medication is applied across domains where additional symptomatic support is needed during symptomatic phases of common bacterial infections.”

Quick Fact: Support for Localized Discomfort

Cephalexin is commonly used to help with infections that cause localized pain, swelling, and redness, helping to improve day-to-day comfort during these symptomatic periods.

Regulatory References

  1. NIH MedlinePlus overview
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Eligibility and Restrictions for Use

Eligibility scope

Populations for whom use is allowed (as stated in label): Adults, older patients, and pediatric patients are allowed use where safety and effectiveness are established.

Populations for whom use is contraindicated: Patients with a known hypersensitivity or allergy to Cephalexin or any other antibiotic in the cephalosporin class must not use this medicine.


Age-related eligibility rules

Safety and effectiveness are established for adults and older adults, though geriatric patients may require special attention due to potential age-related decline in kidney function. For children, use is established, but treatment for infants under one year of age requires a healthcare provider to carefully determine use and dose.


Condition-specific eligibility rules

Use requires caution in individuals with markedly impaired renal function to avoid drug accumulation and potential toxicity. Caution is also advised for patients with a history of gastrointestinal diseases, particularly colitis, due to the documented risk of C. difficile-associated diarrhea. A history of penicillin allergy necessitates caution due to potential cross-sensitivity with cephalosporins.


Pregnancy and lactation eligibility status (if explicitly documented)

Cephalexin is classified as Pregnancy Category B by the U.S. FDA. It should be used during pregnancy only if clearly needed. The drug is excreted in human milk, and official labeling advises caution for nursing mothers.

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What should I know about interactions with other medicines?

Interactions with other medicines and products

Official regulatory information for Cephalexin focuses primarily on interactions that alter drug concentrations or increase the risk of specific toxic effects. No medicine is formally designated as contraindicated for co-administration with Cephalexin based on interaction risk alone.

Pharmacokinetic and Transporter Interactions

The co-administration of probenecid reduces the renal excretion of Cephalexin by inhibiting tubular secretion, which officially results in an increase in Cephalexin's plasma concentrations. Similarly, when taken with metformin, Cephalexin alters the disposition of metformin, leading to documented increases in metformin's mean maximum plasma concentration and Area Under the Curve (AUC).

Pharmacodynamic and Toxicity Risks

There is a documented risk of additive nephrotoxicity when Cephalexin is concurrently administered with other nephrotoxic agents, such as potent diuretics like furosemide or aminoglycosides. Furthermore, Cephalosporins, including Cephalexin, may be associated with a fall in prothrombin activity, which may be relevant when co-administered with anticoagulants such as warfarin.

Administration Requirements

An administration constraint exists for non-drug substances: zinc supplements and products containing zinc require separation of at least 3 hours from Cephalexin intake to prevent reduced absorption. Cephalexin may also decrease the effectiveness of hormonal oral contraceptives.

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Mechanism of Action

How Keflin (Cephalexin) Works

The action of Cephalexin involves interfering with the biological processes that maintain the structural integrity of the bacterial cell. This mechanism is primarily bactericidal, meaning it actively kills the susceptible bacteria rather than merely halting their growth.


Molecular Target: Irreversible Deactivation of Transpeptidases

Cephalexin functions by selectively binding to Penicillin-Binding Proteins (PBPs), which are bacterial enzymes (specifically transpeptidases) located within the cell wall structure. The drug acts as a covalent inhibitor, forming a stable, permanent chemical bond with the PBP active site. This deactivation prevents the enzyme from performing its essential role in peptidoglycan cross-linking, which is the final step in synthesizing the bacterial cell wall.


Mechanistic Cascade: Cell Wall Failure and Osmotic Lysis

The structural failure resulting from PBP inhibition initiates a rapid, destructive cascade. By preventing the construction of the rigid, stabilizing mesh of the cell wall, the drug exposes the bacterium to its own high internal pressure. This leads to immediate loss of osmotic control, causing the bacterial cell to swell and burst (lysis). This targeted destruction directly and rapidly results in the lysis of the susceptible bacterial cell.

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Dosage and Administration Information

Official Administration Guidelines for Cephalexin

Cephalexin is administered exclusively by the oral route in the form of capsules, tablets, or a powder for oral suspension. The correct use of this medicine is defined by specific protocols for dosing, timing, and population-based adjustments.


Dosage and Timing

The standard adult dosage regimen typically involves unit doses of 250 mg or 500 mg, administered in divided doses throughout the day. The official dosage range is generally between 1 gram (1,000 mg) and 4 grams (4,000 mg) daily. Common dosing schedules require taking the medicine every 6 hours or every 12 hours.

The medication is acid-stable and is officially taken without regard to meals.


Course Duration and Special Use

Treatment is administered for a fixed duration, usually ranging from 7 to 14 days. For infections caused by beta-hemolytic streptococci, the course must be administered for a minimum of 10 days.

Population-Specific Rules:

  • Pediatric patients (over 1 year of age) are dosed based on body weight (mg/kg/day), given in equally divided doses.
  • Renal impairment requires specific dose or interval adjustments in adults with severely reduced kidney function (Creatinine clearance < 30 mL/min), where the maximum daily dose may be reduced to 1 gram.

Administration Protocol:

For the liquid suspension, the powder must be reconstituted with water at the time of dispensing and shaken well before each dose is measured and taken. If a dose is missed and it is near the time for the next scheduled dose, the missed dose is skipped to avoid a double dose.

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Recent Clinical Evidence

Keflin (Cephalexin): Recent Clinical Evidence

Evidence for Use in Skin and Soft Tissue Infections

Research exploring this medicine's use in skin and soft tissue infections includes Randomized Controlled Trials (RCTs) and various comparative studies. These studies primarily enrolled adults presenting in outpatient settings with uncomplicated infections. Researchers documented measurements of clinical endpoints, such as whether patients met the definition of clinical cure and the frequency of requiring a step-up to intravenous antibiotics. Follow-up durations were often limited to short intervals, and little research exists for immunocompromised individuals or those with complex skin conditions.

Evidence for Use in Urinary Tract Infections

Research has explored the use for uncomplicated urinary tract infections using comparative trials and retrospective studies, often focusing on adult women with acute cystitis. The research examined endpoints such as treatment failure and patterns related to the causative bacteria. Data show patterns related to symptom evolution and recurrence within a 30-day follow-up period. Evidence is limited for complicated infections or patients with underlying urologic issues.

Evidence for Use in Respiratory Tract and Ear Infections

The evidence base for using this medicine in certain respiratory tract infections and Otitis Media is built upon historical clinical trials and contemporary comparative studies, often involving pediatric patients. Studies monitored outcomes like clinical response, bacteriological cure rates, and the frequency of relapse. Comparative data indicates that measured outcomes related to treatment may vary depending on the specific bacterial strain observed in the research.

Studies Addressing Long-Term Outcomes and Durability

The research was evaluated in studies conducted during the acute phase of an infection; the follow-up durations were limited in most pivotal trials. Long-term effects are not fully established, and research does not determine whether an individual will respond similarly in terms of sustained effect over many months or years.

Evidence in Special Patient Populations

Research examined use in pediatric patients and older adults. However, the sample sizes were modest for many trials, and data for certain groups remain insufficient. Individuals with significant comorbidities were frequently excluded from participation in the major clinical trials.

Key Research Gaps and Uncertainties

The evidence quality varies across studies, particularly between the older and more recent comparative trials. Data for certain groups remain insufficient, such as those with underlying problems with overall body function, due to high exclusion rates in clinical trials. Research provides context but not individual predictions for patient outcomes.

Key Studies & References

  1. Label: CEPHALEXIN tablet (FDA DailyMed)
  2. Twice daily cephalexin for uncomplicated urinary tract infection in women (Retrospective cohort study)
  3. Cephalexin - StatPearls (NCBI Bookshelf)
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Frequently Asked Questions (FAQ)

Common questions about Keflin (Cephalexin) (FAQ)

Q: What are the main types of bacterial infections Keflin (Cephalexin) is prescribed to treat?

Official prescribing information indicates that this medicine is used for infections caused by susceptible bacteria in several key areas. These include the respiratory tract, middle ear (otitis media), skin and skin structure, bone, and the genitourinary tract. Official documents list indications based on the susceptible bacteria identified.

Q: Is Keflin (Cephalexin) a type of penicillin?

According to official regulatory information, Keflin (Cephalexin) is a cephalosporin antibiotic. It belongs to the same general drug family, the beta-lactam class, as penicillin. Due to the potential for cross-sensitivity among these antibiotics, official safety documents state caution is required in patients with a history of penicillin allergy.

Q: Can Keflin be used for viral infections like the common cold or flu?

No. Regulatory documents confirm that Cephalexin is a specific antibacterial medicine designed to kill susceptible bacteria. It will not work for viral infections, such as the common cold or flu. Official labeling states using it for a viral illness is not indicated and can contribute to the development of drug-resistant bacteria.

Q: What is the difference between the brand name Keflin and the generic Cephalexin?

Cephalexin is the name of the active drug ingredient and is the International Nonproprietary Name (INN) for the compound. Keflin is a historical brand name under which this active ingredient was or is sold. Both names refer to the same therapeutic substance.

Q: Is Keflin (Cephalexin) effective against staph infections?

Yes, official labeling indicates that Cephalexin is effective for treating infections caused by susceptible isolates of Staphylococcus aureus in areas like the skin and bone. However, the medicine is not effective against strains that are resistant, such as methicillin-resistant staphylococci (MRSA).

Q: Is developing a yeast infection a common side effect of Keflin (Cephalexin)?

Regulatory-derived safety information reports that vaginal yeast infections are known adverse effects associated with the use of this antibiotic. Patients may also report related symptoms such as vaginal itching or discharge. This is a known risk when taking antibiotics, which can disrupt the body's natural balance of bacteria.

Q: What are the signs of a serious or severe allergic reaction to Keflin?

Official prescribing information identifies rare but serious allergic events, such as anaphylaxis. Reported symptoms of anaphylaxis may include hives, difficulty breathing, or swelling of the face, tongue, or throat. Additionally, severe skin reactions have been reported, which can involve symptoms like fever, skin pain, and blistering.

Q: Can Keflin (Cephalexin) cause severe diarrhea, and what should a patient watch for?

A severe form of bowel inflammation, known as pseudo-membranous colitis, is a rare but serious adverse reaction reported with Cephalexin. This condition can potentially occur even after the medicine course has ended. Reported signs can include watery or bloody diarrhea and severe abdominal pain.

Q: Is it necessary to use an alternative form of birth control while taking Keflin?

Official documents state that cephalosporins, which include Cephalexin, may decrease the effectiveness of hormonal oral contraceptives. This information is provided in regulatory documents to describe the potential for reduced effectiveness.

Q: Does Keflin (Cephalexin) interact with alcohol?

The official FDA prescribing information for Cephalexin does not list a direct drug-alcohol interaction. Regulatory sources do not list a direct interaction; however, common side effects like dizziness and nausea may be worsened by alcohol.

Q: Are there any known interactions between Keflin and common over-the-counter pain relievers?

Regulatory screening does not indicate a clinically significant interaction between Cephalexin and common over-the-counter pain relievers such as acetaminophen. The medicine's absorption is reduced by zinc supplements, which regulatory documents state require a separation of at least 3 hours.

Q: How soon after starting Keflin will I typically start to feel better?

Official information indicates that, based on pharmacokinetic studies, the medicine reaches its peak concentration in the blood around one hour after dosing. However, it may take up to 48 hours (two days) before symptoms related to the infection begin to show signs of abating.

Q: What happens if a person stops taking Keflin before they complete the full course?

Regulatory labeling emphasizes the necessity of completing the entire prescribed course of medicine. This is noted in regulatory guidelines as necessary to reduce the development of drug-resistant bacteria and to maintain effectiveness against the original infection being treated.

Q: Why is it important to take every dose of Keflin exactly as prescribed?

Official guidance states that taking the medicine exactly as prescribed is important to maintain adequate concentration levels of the drug in the body. Consistent dosing helps maintain drug levels necessary to treat the infection and works to reduce the development of drug-resistant bacteria over the course of the treatment.

Q: Can Keflin use lead to a person developing antibiotic resistance?

Regulatory documents explicitly address the need to reduce the development of drug-resistant bacteria. Official warnings state that prolonged use of Cephalexin may result in the overgrowth of nonsusceptible organisms, which is a form of resistance or secondary infection.

Q: Can Keflin interfere with the results of certain laboratory blood or urine tests?

Official prescribing information notes that Cephalexin may cause interference with certain laboratory tests. This includes tests for measuring urine sugar (glucose), which may sometimes result in a false-positive reading.

Q: Are there any specific foods or drinks that should be avoided with Keflin (Cephalexin)?

Official documents state that the medicine can be taken without regard to meals. The primary non-drug administration constraint is that the medicine’s absorption is reduced by zinc supplements, which regulatory documents state require a separation of at least 3 hours.

Q: Does Keflin cause dizziness or difficulty concentrating?

Regulatory-derived safety information reports that side effects such as dizziness and headache are possible adverse reactions associated with this medicine. Official reports do not commonly list difficulty concentrating as an adverse reaction.

Q: Can Keflin be used for long-term suppressive therapy in some conditions?

Official warnings state that prolonged use of Cephalexin may result in the overgrowth of nonsusceptible organisms (superinfection). The usual duration of treatment described in administration guidelines is short-term, typically ranging from 7 to 14 days.

Q: Does Keflin have a high or low risk of causing sensitivity to the sun?

According to official safety information and comparative safety guidelines, Cephalexin is not typically associated with a risk of photosensitivity, which is an increased sensitivity to sun exposure. It does not carry the sun exposure warnings common with some other antibiotic classes.

Q: Is feeling unusually tired or weak a known side effect of Keflin?

Regulatory-derived safety information reports that fatigue or unusual tiredness are known side effects that have been reported with the use of Cephalexin.

Q: Is there any research about Keflin and potential developmental effects in babies or children?

The U.S. FDA classifies the drug as Pregnancy Category B, meaning studies have not demonstrated a risk to the fetus. However, its use during pregnancy is described as acceptable only when clearly needed. Separately, safety and effectiveness are formally established for children over one year of age.

Q: Can Keflin cause headaches or joint pain?

Regulatory-derived safety information reports that headache is a possible adverse reaction. Joint problems (arthralgia) are also mentioned in safety reporting, though they are generally classified as rare or serious effects.

Q: Is Keflin (Cephalexin) generally considered a broad-spectrum or narrow-spectrum antibiotic?

Cephalexin is classified as a first-generation cephalosporin. It is primarily effective against susceptible Gram-positive bacteria and is generally considered to have a relatively narrow spectrum of activity compared to newer generation antibiotics.

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How should Keflin (Cephalexin) be stored and disposed of?

Official Storage and Disposal Profile

The required storage environment for Cephalexin is defined by its dosage form to maintain potency and stability, as outlined in regulatory documentation.

Dosage Form Required Storage Condition
Capsules/Tablets Controlled Room Temperature (20 C–25 C)
Reconstituted Suspension Refrigeration (2 C–8 C)

Solid dosage forms must be protected from excessive moisture and heat. The liquid suspension must not be frozen.

Stability and Handling

The reconstituted oral suspension has a strict 14-day discard limit and must be thrown away after this period, even if medication remains. All Cephalexin products must be stored in a tightly closed container and kept out of the reach of children for safety.

Disposal

Unused or expired Cephalexin must be disposed of according to local regulations or returned via an approved drug take-back program.

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

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