Clarithro

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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.

Overview of Clarithro

Quick Facts

Property Description
Active ingredient Clarithromycin
Form Tablet (IR/ER), Oral Suspension, Solution for Injection
Pharmacological class Macrolide Antibiotic (Antibacterial)
General Purpose Countering unwanted bacterial infections
Origin Semisynthetic (derived from Erythromycin)

What is Clarithro: Defining the Medicine and Its Origin

Clarithro is a medicinal product that contains the active ingredient Clarithromycin, which is chemically defined as a semisynthetic macrolide antibiotic. This medication's general purpose is to counteract the proliferation of unwanted bacterial presence by inhibiting the growth of susceptible organisms, thereby functioning as an antibacterial agent. The drug is utilized as a primary agent for managing respiratory infections when a macrolide is indicated.

Clarithromycin is classified as semisynthetic because it is derived from the natural compound Erythromycin, but chemically modified to improve its properties. This modification confers enhanced acid stability, which facilitates more consistent absorption when the drug is taken orally. As a single-ingredient product, Clarithro delivers its therapeutic effect exclusively through the action of Clarithromycin and its active metabolite.


What Pharmacological Class Does Clarithro Belong To?

Clarithro belongs to the macrolide pharmacological class, a group of antimicrobials distinguishable by their specific chemical structure. Its core mechanism involves functioning as a protein synthesis inhibitor; it selectively binds to the 50S ribosomal subunit of the bacterial cell, thereby preventing the bacteria from creating the proteins necessary for survival and replication. This action is generally bacteriostatic, meaning it stops the proliferation of the bacteria. Clarithromycin is a macrolide that works by inhibiting bacterial protein synthesis.


Available Forms of Clarithro

The medicinal entity Clarithromycin is manufactured in several distinct dosage forms to facilitate various route(s) of administration. These forms include conventional tablets for immediate release, specialized extended-release tablets, and an oral suspension (prepared from granules or powder) primarily for pediatric patients. The drug is also available as a solution for injection for intravenous (IV) use when acute administration is required in clinical settings.

What side effects are possible with Clarithro?

Adverse Reaction Scope

The most frequent adverse reactions reported for Clarithro (Clarithromycin) in clinical trials involve the gastrointestinal system and the nervous system. Adverse events are formally classified in regulatory documents by frequency and affected System-Organ-Class (SOC), consistent with ICH/EMA standards.

Frequency Classification Examples (SOC Categories)
Common (ge 1/100 to < 1/10) Nausea, vomiting, diarrhea, abdominal pain, headache, dysgeusia (taste perversion), and insomnia.
Uncommon (ge 1/1,000 to < 1/100) Candidiasis, anxiety, vertigo, rash, pruritus, and elevated liver enzymes.
Not Known (Post-marketing data) Fatal hepatic failure, Torsade de Pointes, acute pancreatitis, and reversible deafness.

Serious Adverse Reactions and Safety Restrictions

The regulatory label explicitly documents the potential for rare, but clinically serious adverse reactions, which include severe hepatotoxicity (such as hepatic failure), QT interval prolongation leading to ventricular arrhythmias like Torsade de Pointes, and severe cutaneous reactions (SCAR) such as Stevens-Johnson Syndrome.

Clarithro is formally contraindicated in patients with a history of QT prolongation or ventricular arrhythmia, and those with uncorrected electrolyte disturbances (hypokalemia or hypomagnesemia). Use is also restricted for patients taking certain interacting medications, notably lovastatin, simvastatin, or colchicine, due to risks like rhabdomyolysis or severe toxicity.

Population-Specific Safety

Safety notes specify that dosage adjustment is required for patients with severe renal impairment (creatinine clearance < 30 mL/min). Caution is advised in patients with impaired hepatic function, and the medicine is generally contraindicated in patients with severe hepatic failure combined with renal impairment. Elderly patients are noted to be more susceptible to drug-associated effects on the QT interval.

Connection to the Overall Safety Profile

The official safety profile differentiates between common, non-serious gastrointestinal and sensory disturbances and rare, severe risks like cardiac and hepatic events that necessitate specific usage restrictions. This regulatory classification system ensures all documented risk characteristics and limitations are communicated in a standardized, medically grounded format.

Overdose and Emergency Response

Overdose and when to seek help

The official regulatory documentation describes specific clinical signs and required actions in the event of a Clarithromycin overdose. Documented overdose presentations commonly involve severe gastrointestinal distress, including abdominal pain, nausea, vomiting, and diarrhea. Further documented acute manifestations can include transient sensory changes like dysgeusia (altered taste) and transient hearing loss.

Overdose presents a risk of severe systemic outcomes affecting the cardiovascular and hepatic systems. The most serious concern is the potential for QT interval prolongation, which can escalate to life-threatening ventricular arrhythmias, including Torsades de pointes, and hepatic failure. Elderly patients and individuals with existing cardiac risk factors are noted as potentially more susceptible to these cardiac effects.

Due to the potential for these severe complications, the official guidance mandates that individuals must seek emergency medical attention immediately upon recognition of an acute overdose. Management is constrained to symptomatic and supportive treatment and may involve procedures like gastric lavage to remove unabsorbed drug. Regulatory information states that no specific antidote for Clarithromycin overdose is known, and continuous ECG monitoring is required due to the cardiac risk.

Therapeutic Uses of Clarithro

This medication is generally used in situations involving certain distressing symptoms. Clarithro is applied across domains where additional symptomatic support is needed, addressing symptom clusters that may become intense or disruptive. It is commonly used to help with conditions presenting with acute episodes like bacterial pneumonia, acute bronchitis, sinusitis, and otitis media. It is also relevant for managing skin and soft tissue infections such as cellulitis, and plays a role in protocols for the eradication of H. pylori and the management of Mycobacterium avium Complex (MAC) disease. The medication is relevant for managing symptoms that interfere with daily comfort, such as fever, persistent cough, and localized pain.

“It offers symptomatic relief that supports patients during episodes of heightened discomfort.”

This assistance is crucial during phases when symptoms become more noticeable, contributing to improved comfort during periods of heightened symptoms.

Quick Fact: Relief for Acute Discomfort
Primary Goal Provides support that helps ease the overall symptom burden.
Domain Example Respiratory, skin, and ENT infections.
Symptom Focus Fever, pain, inflammation, and chest discomfort.

Regulatory References

  1. MedlinePlus Drug Information

Eligibility and Restrictions for Use

Eligibility Profile: Official Regulatory Information

Clarithro (Clarithromycin) is subject to strict eligibility rules documented in official government prescribing information. Use is contraindicated in specific patient populations due to the risk of serious adverse events.

Population Status Regulatory Rule
Populations Contraindicated Patients with known macrolide hypersensitivity; a history of cholestatic jaundice or hepatic dysfunction linked to prior Clarithromycin use; and those with pre-existing QT prolongation or ventricular cardiac arrhythmias. Use is also prohibited with severe hepatic failure combined with renal impairment.
Restricted or Conditional Use Patients with severe renal impairment (creatinine clearance < 30 mL/min) are eligible only with a mandated dose reduction. Caution is advised for patients with Myasthenia Gravis or underlying coronary artery disease.
Age Group Eligibility The medicine is approved for adults and adolescents (12 years and older). For children 6 months to 12 years, the oral suspension formulation is typically used. Safety and efficacy are not established for infants under 6 months of age.
Pregnancy and Lactation Use is not advised in pregnant women without carefully weighing the benefits against the risk, particularly during the first trimester. Clarithromycin is not recommended for use while breastfeeding.

The most severe restrictions relate to co-administration with numerous prohibited drugs, including Lovastatin, Simvastatin, Ergot Alkaloids, and Pimozide. Patients must not use Clarithromycin if they have uncorrected hypokalaemia or hypomagnesaemia.

What should I know about interactions with other medicines?

Interactions with other medicines and products

Clarithro can interact with numerous medicinal products, primarily because it is a strong inhibitor of the CYP3A4 enzyme and a substrate and inhibitor of P-glycoprotein (P-gp). These mechanisms can significantly increase the plasma concentrations of co-administered drugs that are metabolized by this pathway or transported by P-gp.

Contraindicated Combinations

Official regulatory documents require that Clarithro must not be used with the following medicines due to the risk of serious or life-threatening reactions:

Classification Examples of Prohibited Medicines
HMG-CoA Reductase Inhibitors Simvastatin, Lovastatin
Ergot Alkaloids Ergotamine, Dihydroergotamine
Other Medicines Cisapride, Pimozide, Lurasidone, Lomitapide

Co-administration with Colchicine is also contraindicated in patients who have pre-existing renal or hepatic impairment.

Clinically Significant Interactions

Co-administration with certain medicines requires caution, monitoring, and often dosage adjustment of the interacting drug. These include oral anticoagulants (like Warfarin), immunosuppressants (like Cyclosporine, Tacrolimus), and some calcium channel blockers (like Verapamil).

Clarithro should be used cautiously with other drugs that prolong the QT interval (e.g., Amiodarone, Quinidine) due to the potential for additive cardiac effects. Additionally, co-administration with CYP3A enzyme inducers (e.g., Rifampicin, Carbamazepine) can reduce Clarithro levels, potentially decreasing its effectiveness.

Mechanism of Action

How Clarithro Works

Clarithromycin (Clarithro) exerts its core action as a semisynthetic macrolide by interfering with the vital biological processes of susceptible bacteria. Its mechanism is highly specific and is based on two primary domains of action.


Inhibiting the Bacterial Protein Manufacturing Line

Clarithromycin's primary mechanism involves the molecular targeting of the bacterial ribosome. The drug and its active metabolite selectively bind to the 50S ribosomal subunit within the bacterial cell. This binding action physically blocks the exit tunnel required for the construction of new proteins, inhibiting the synthesis of proteins required for metabolic function and replication. This interference initiates a mechanistic cascade resulting in a bacteriostatic effect—the growth of the bacterial population is arrested.


Evasion of the Ribosomal Target (Mechanistic Limitations)

The mechanism's function is constrained by biological limitations, primarily centered on bacterial defense mechanisms. In some cases, resistance develops through target modification, such as methylation of the binding site on the 23S rRNA, which prevents the drug from binding. Other bacteria use efflux pumps to actively expel the drug from the cell before it can reach the 50S ribosomal target. These intrinsic mechanisms of evasion override the drug's core function, resulting in the continued function of the bacterial proliferation pathway.

Dosage and Administration Information

How Clarithro is Used: Official Administration Guidelines

Clarithro (clarithromycin) is administered via oral or intravenous (IV) infusion routes, according to the specific formulation and clinical context. The official use instructions define the precise dose, frequency, and duration for the medicine.


Standard Labeled Dosing and Frequency

Administration Form Standard Adult Dose Frequency Duration (Typical)
Immediate-Release (IR) Tablets 250 mg or 500 mg Every 12 hours 7 to 14 days
Extended-Release (ER) Tablets 1 gram (1000 mg) Every 24 hours (Once Daily) 7 to 14 days
IV Infusion (Hospital Use) 500 mg Every 12 hours Short-term

For pediatric patients (typically 6 months to 12 years), the oral suspension is used, with a daily dosage of 15 mg/kg divided into two doses (every 12 hours), usually for 10 days.


Administration Conditions and Adjustments

The following conditions for use are standard clinical requirements:

  • With/Without Food: Immediate-release forms (tablets and suspension) may be taken with or without food. Extended-release tablets, however, must be taken with food.
  • Handling: Extended-release tablets must be swallowed whole and must not be chewed, broken, or crushed to maintain their release mechanism.
  • Renal Impairment: In cases of severe renal impairment (CLcr < 30 mL/min), the labeled dosage must be reduced by 50% (e.g., 250 mg once daily for the standard dose), and the duration should not exceed 14 days.
  • IV Procedure: The intravenous formulation must be administered as a slow infusion over 60 minutes; rapid injection or bolus administration is not permitted by official instructions.

Recent Clinical Evidence

Clarithro: Recent Clinical Evidence

The research base for Clarithromycin primarily consists of short-term Randomized Controlled Trials (RCTs) and comparative studies, which examined clinical response rates and the rate at which targeted bacteria were observed in patient populations. These studies monitored outcomes related to systemic or functional imbalance caused by infection.

For common conditions associated with acute episodes, such as Community-Acquired Pneumonia (CAP) and bronchitis, research focused on adults and pediatric patients, tracking outcomes like fever resolution and bacteriological eradication over a typical 7 to 14-day treatment window. The evidence for these primary indications is generally categorized as high-level, though results apply only to the populations studied.

The drug was also studied for complex combination protocols, including the definitive eradication of H. pylori and as part of multi-drug regimens for Mycobacterium avium Complex (MAC) disease in immunocompromised patients. A key limitation acknowledged in the research across these infectious disease indications is the variability of reported success rates due to rising levels of antibiotic resistance.

Regulatory reviews have highlighted a specific area of long-term research concerning stable coronary heart disease (CHD). One large, prospective RCT observed a pattern of potential long-term association with increased all-cause death after short exposure. However, subsequent observational studies attempting to replicate this signal reported mixed findings. Certainty remains low for this specific pattern, as no clear biological explanation has been established and the evidence is limited to this highly specific population. Research is ongoing to address these gaps.

Frequently Asked Questions (FAQ)

Common questions about Clarithro (FAQ)

Q: What is the main reason doctors prescribe Clarithro?

Clarithro is an antibiotic prescribed primarily for treating mild to moderate infections caused by certain susceptible bacteria. These include upper and lower respiratory tract infections, such as community-acquired pneumonia, acute bacterial exacerbation of chronic bronchitis, and sinusitis. It is also used in specific combination therapies.

Q: Is Clarithro considered a type of antibiotic?

Yes, Clarithro is classified as a macrolide antimicrobial agent, which is a specific class of antibiotics. Its intended purpose is to treat infections caused by bacteria, not viruses.

Q: How quickly does Clarithro usually start working?

According to official product information, the active substance is absorbed relatively quickly after the medicine is taken orally. Peak concentrations of the substance in the bloodstream are typically reached within two to three hours after dosing.

Q: How long does it typically take for Clarithro to clear up an infection?

The time it takes to clear an infection depends on the type and severity of the condition being treated. Regulatory guidelines define the entire course of therapy, which typically lasts from 7 to 14 days, as necessary for treatment.

Q: Is it true that Clarithro can cause a metallic taste?

Yes, taste perversion, or dysgeusia, is a common adverse reaction reported in clinical trials. This effect can often be described as having a persistent metallic taste in the mouth while taking the medicine.

Q: What are the most common side effects people report when taking Clarithro?

Official clinical trial data lists the most frequent adverse reactions for adults and children. These commonly include abdominal pain, diarrhea, nausea, vomiting, and taste perversion.

Q: Does Clarithro cause drowsiness or affect my ability to drive?

While the medicine is not typically classified as a sedative, dizziness has been reported as an adverse reaction in clinical studies. Official safety information notes that individuals may experience effects that could influence their ability to drive or safely operate machinery.

Q: Is there a difference between Clarithro and Azithromycin?

Both are macrolide antibiotics used to treat bacterial infections, but they are different medicines. Clarithro is specifically noted in regulatory information as being a potent inhibitor of the CYP3A4 enzyme, which affects how it interacts with other drugs, distinguishing it pharmacologically from other macrolides like Azithromycin.

Q: Do I need to take Clarithro with food, or is it better on an empty stomach?

The instructions depend on the formulation. Immediate-release tablets can be taken with or without food. However, regulatory documents specify that the extended-release tablets are to be administered with food.

Q: What happens if I miss a dose of Clarithro?

Official administration guidelines emphasize the importance of taking the medicine regularly to maintain consistent levels of the substance in the body. If you miss a dose, a healthcare professional can provide guidance on the correct procedure for your specific situation.

Q: What are the concerns about taking Clarithro with statins or cholesterol medicine?

Clarithro is contraindicated for use with certain cholesterol-lowering medicines, specifically lovastatin and simvastatin. This combination can significantly increase the concentration of the statin in the blood, which raises the risk of severe muscle side effects.

Q: Can Clarithro affect the effectiveness of birth control pills?

Clarithro is known to inhibit the hepatic microsomal CYP3A4 enzyme, which is involved in the metabolism of many medicines, including some hormonal products. The labeling describes the potential for interaction, and this is a topic to be discussed with a healthcare provider.

Q: Can Clarithro be used to treat viral infections like the flu or common cold?

No. Clarithro is an antibiotic that only targets infections caused by susceptible bacteria. Official drug information states that it is not effective against viral infections, such as the common cold or the flu.

Q: Is Clarithro safe for children?

Official drug labels include specific dosing guidelines for pediatric patients (usually 6 months and older) for selected conditions. The medication is only prescribed for children under the supervision of a medical professional, who assesses its appropriateness for the child's specific condition.

Q: Why does Clarithro sometimes interact with heart medications?

Clarithro has been associated with prolongation of the QT interval, which is an effect that can lead to serious heart rhythm changes. Because of this, the medicine is contraindicated with other drugs that are known to prolong the QT interval.

Q: Can I stop taking Clarithro once my symptoms improve?

The course of therapy is defined by a specific duration. Following the entire prescribed course is necessary to minimize the potential for developing drug-resistant bacteria.

Q: Is Clarithro the same as erythromycin?

Clarithro is a semi-synthetic macrolide antibiotic that is chemically derived from erythromycin. It is in the same class of medicines but has different properties, including pharmacokinetic profiles and drug interaction potential.

Q: Can older adults or elderly people safely take Clarithro?

Official prescribing information contains specific considerations for geriatric use. Older adults may be more susceptible to effects on the heart's rhythm (QT prolongation). The decision to use it is based on the prescribing physician's assessment.

Q: Is it common for people to have diarrhea when taking Clarithro?

Diarrhea is a common adverse reaction reported in clinical trial data. Official safety information also describes the risk of severe diarrhea associated with Clostridium difficile, a condition associated with the use of nearly all antibiotics.

Q: Are there any known issues with taking Clarithro while pregnant or breastfeeding?

Clarithro is generally not advised for use during pregnancy unless the supervising physician determines that the potential benefit outweighs the potential risk. The product information describes that the medicine is excreted in human breast milk, and this requires medical consideration.

Q: Can Clarithro be used to treat Helicobacter pylori (H. pylori) infections?

Yes, Clarithro is indicated as part of a multi-drug regimen, typically known as triple therapy, for the treatment of H. pylori infections associated with duodenal ulcers.

Q: What are the signs of an allergic reaction to Clarithro?

Official labeling describes severe allergic reactions, such as anaphylaxis and severe skin rashes. These reactions are considered serious safety risks and require immediate medical attention as outlined in the safety information.

Q: Does Clarithro interact with herbal supplements like St. John’s Wort?

Yes. St. John’s Wort is described in drug interaction resources as an inducer of the CYP3A enzyme. This could potentially reduce the concentration of Clarithro in the body, making it less effective.

Q: Is Clarithro often prescribed for bronchitis or pneumonia?

Yes, regulatory documents indicate that Clarithro is prescribed for the treatment of mild to moderate infections in the lower respiratory tract. This includes acute bacterial exacerbation of chronic bronchitis and community-acquired pneumonia, when caused by susceptible organisms.

Q: What kind of kidney or liver conditions prevent someone from using Clarithro?

The medicine is contraindicated in patients with a history of cholestatic jaundice or hepatic dysfunction (liver problems) associated with prior use of the drug. Dosage adjustments are noted in the label as necessary for patients with severe kidney impairment.

Q: Can taking Clarithro cause an overgrowth of yeast or thrush?

Antibiotics, including Clarithro, work by targeting bacteria, which can change the normal balance of micro-organisms in the body. This alteration can sometimes lead to the overgrowth of other organisms, such as yeast (candidiasis) or Clostridium difficile.

Q: How should I store Clarithro tablets or suspension?

Official storage instructions advise that Clarithro tablets should be stored at controlled room temperature, typically between 20 and 25 C. The labeling instructs that the tablets be kept protected from light and the container remain tightly closed.

Q: Why is it important to finish the entire course of Clarithro?

Following the entire course is necessary to minimize the potential for developing drug resistance.

Q: Can I take Clarithro if I have a history of heart rhythm problems?

No. Official prescribing information lists a history of heart rhythm problems, including known QT prolongation or ventricular cardiac arrhythmia, as a strict contraindication for using Clarithro.

Q: Is Clarithro known to cause headaches or dizziness?

Yes, headache and dizziness are reported adverse reactions in clinical trial data. These are adverse events documented in the safety section of the product labeling.

Q: What does 'macrolide antibiotic' mean in simple terms?

A macrolide is a class of antibiotic named for its chemical structure. These medicines work by disrupting the bacteria's ability to produce the essential proteins they need to grow and multiply, thereby stopping the infection.

Q: How is Clarithro involved in combination therapy for certain conditions?

Clarithro is indicated as part of a combination regimen for treating certain conditions, most notably H. pylori infections. It is also used with other anti-mycobacterial drugs for treating Mycobacterium avium complex infections.

Q: Is it safe to take Clarithro if I'm allergic to penicillin?

Clarithro is a macrolide and is chemically distinct from penicillin. For patients with a known allergy or hypersensitivity to penicillin, macrolides are often cited as a common alternative class of antibiotics.

Q: Are there different brand names for Clarithro?

Yes, Clarithro is the generic name for the drug clarithromycin. It has been sold and marketed under various different brand names globally, depending on the pharmaceutical manufacturer.

Q: Is there a difference in side effects between the immediate-release and extended-release versions?

While regulatory documents distinguish the two formulations by their different dosing and release profiles, a direct comparison of their side effect profiles is not consistently listed. Patients are directed to review the prescribing information for each specific formulation to access the respective clinical trial data.

Q: Does Clarithro interact with blood thinners like warfarin?

Yes, official labeling notes an interaction with oral anticoagulants, such as warfarin. The official label specifies that co-administration with anticoagulants requires close monitoring of the blood’s clotting time by a healthcare professional.

Q: Can Clarithro cause insomnia or changes in sleep patterns?

Adverse reactions affecting the central nervous system, such as confusion, have been reported in regulatory documents. While insomnia is not consistently listed as a frequent side effect, changes in sleep patterns may be related to these reported central effects.

Q: Why is Clarithro sometimes used for mycobacterial infections?

Clarithro is indicated specifically for the treatment and prophylaxis (prevention) of disseminated or localized infections caused by Mycobacterium avium complex (MAC). This is a type of infection that typically affects individuals with weakened immune systems.

Q: What percentage of patients experience severe side effects from Clarithro?

Official clinical trial data provides incidence rates for many common adverse reactions. For example, reports show that diarrhea and taste perversion were each experienced by about 8% of adult patients, and nausea by 11%. This information is used to help describe the general expectations of using the medicine.

Q: Does Clarithro make other medications stay in the body longer?

Yes. Clarithro inhibits the hepatic microsomal CYP3A4 isoenzyme. This can reduce the body's ability to clear other medicines that are metabolized by this enzyme, potentially leading to higher concentrations of those drugs.

Q: What does the research say about Clarithro's use in younger children?

The official product label provides specific dosing recommendations for pediatric patients starting from 6 months of age for select infections. These recommendations are based on clinical studies and data reviewed by regulatory agencies.

Q: Is Clarithro effective against community-acquired pneumonia?

Yes, official regulatory indications state that Clarithro is prescribed for the treatment of mild to moderate community-acquired pneumonia, provided the infection is caused by designated, susceptible bacteria.

Q: Can Clarithro cause changes in taste or smell that last a long time?

Changes in taste (taste perversion) are a reported adverse reaction. The regulatory documentation does not typically provide specific data on the exact duration of the taste changes after the course of therapy has been completed, and this aspect is not well studied.

Q: What are the typical non-infectious conditions people mistakenly think Clarithro treats?

Clarithro is a medicine that acts specifically on bacteria. It is explicitly stated in the official documentation that it is not effective for or indicated to treat conditions caused by viruses, such as the common cold or the flu, which are often the source of user misunderstanding.

How should Clarithro be stored and disposed of?

How to Store and Dispose of Clarithromycin

The storage of clarithromycin is defined by its formulation. Tablets must be stored at controlled room temperature (20 C to 25 C) in the original, tightly closed container, and protected from light. The medicine must be kept out of the sight and reach of children.

Stability and Handling

Once the oral suspension is mixed, it must not be refrigerated or frozen. It should be stored at room temperature (15 C to 30 C) and discarded after 14 days.

Disposal

Unused or expired clarithromycin must be disposed of according to official regulatory guidelines, such as taking it to a medicine take-back program. It should not be disposed of via the wastewater system.

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

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