Maxigan

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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 Maxigan

Property Description
Active ingredient Clarithromycin
Form Tablets (including extended-release) and oral suspension
Pharmacological class Macrolide antibiotic
General purpose Combats susceptible bacterial infections
Origin Semisynthetic

Maxigan: Identity and Pharmacological Class Differentiation

Maxigan is the prescription-only brand name for the medication containing the single active compound, Clarithromycin. It is formally classified as a semisynthetic macrolide antibiotic, belonging to a specific group of drugs clinically recognized for their efficacy against certain bacterial infections. The semisynthetic nature of Clarithromycin is a key feature, as it represents a chemical adaptation of the older, naturally derived erythromycin, resulting in improved acid stability and absorption. As a macrolide, Maxigan is often utilized as an alternative for patients who have known penicillin hypersensitivities.


Composition, Forms, and General Action

Maxigan is offered in several essential dosage forms primarily intended for oral administration, which include standard film-coated tablets and extended-release tablets designed for a less frequent dosing schedule. The granules for oral suspension are a critical formulation element, positioning the drug for effective use in pediatric patient groups and others unable to swallow pills.

Its therapeutic action is achieved by interfering with the bacteria's ability to assemble essential proteins. It does this by binding to the bacteria's internal machinery, specifically the 50S ribosomal subunit. Pharmacological studies have supported that this binding action prevents the pathogen from growing and replicating, confirming its antimicrobial utility. Maxigan's ultimate purpose is to serve as a reliable agent in halting the spread of infection and allowing the body’s immune system to resolve the underlying condition.

What side effects are possible with Maxigan?

Possible Side Effects and Safety Information

The most significant and serious safety concerns associated with Maxigan (commonly identified as Metamizole in international regulatory reviews) primarily involve the blood and immune systems.

Serious Adverse Reactions (Rare)

  • Agranulocytosis: A sudden and sharp decrease in a type of white blood cell, which can lead to life-threatening infections. This reaction is considered rare to very rare but is a critical safety factor. It may occur at any time during treatment, or shortly after discontinuation, and is not related to the dose used.
  • Aplastic Anemia: A severe condition where the bone marrow does not produce enough new blood cells.
  • Severe Hypersensitivity: This includes potentially life-threatening reactions such as anaphylactic shock, bronchospasm, and severe skin conditions (e.g., Toxic Epidermal Necrolysis).
  • Hepatotoxicity: Cases of severe liver injury, including acute hepatitis and acute liver failure, have been reported.

Common Adverse Reactions

Common effects may include nausea, dryness of mouth, dizziness, blurred vision, and sleepiness. The risk of upper gastrointestinal bleeding may be increased compared to baseline.

Population-Specific Safety Considerations

  • Pregnancy and Lactation: Use of the drug is generally advised against during the third trimester of pregnancy due to the potential for adverse effects on the fetus, and during breastfeeding, as the substance is excreted in breast milk.
  • Contraindications: The use of this substance is strictly contraindicated in patients with a history of agranulocytosis or severe hypersensitivity to the drug, patients with acute porphyria, or those with impaired blood cell production.
  • Caution: Special caution is generally advised for use in the elderly and in patients with pre-existing kidney or liver impairment.

Overdose and Emergency Response

The official regulatory documentation for Maxigan (Clarithromycin) overdose details specific expected clinical manifestations and mandates immediate emergency actions. Ingestion of large amounts is expected to produce pronounced gastrointestinal symptoms, including stomach pain, nausea, vomiting, and diarrhea. Rare, severe intoxication cases documented in official labeling have also involved signs such as altered mental status, paranoid behaviour, hypoxaemia, and hypokaliaemia.

Official Mandate Symptom / Scenario
Call Emergency Services (911) Collapse, seizure, trouble breathing, or inability to be awakened
Contact Poison Control Any suspected overdose

The guidance strictly requires you to call emergency services immediately if life-threatening symptoms occur. The officially described medical intervention is symptomatic and supportive treatment, aimed at the prompt elimination of unabsorbed drug. Regulatory documents note that no specific antidote is known for Maxigan overdose. Furthermore, regulatory data indicate that there are no available findings to support the effective removal of the drug via hemodialysis or peritoneal dialysis procedures.

Therapeutic Uses of Maxigan

Maxigan is commonly used in conditions characterized by periods of heightened symptoms caused by susceptible bacteria, and may be part of symptomatic management across several domains. It is applied across domains where additional symptomatic support is needed to address symptom clusters that may become intense or disruptive.

Maxigan is considered relevant in clinical settings that involve acute or unstable symptom patterns, including infections of the respiratory tract (like strep throat, sinusitis, and pneumonia), skin and soft tissues (like cellulitis), and acute otitis media (ear infection). It is also used as an essential therapeutic alternative for susceptible infections when patients have a known penicillin hypersensitivity, providing supportive relief when symptoms interfere with routine activities.

The medication may help address symptoms that appear suddenly or fluctuate, providing support that contributes to improved day-to-day comfort.

The medication supports the patient during difficult episodes by easing distress and may assist in symptom stabilization when used in complex regimens, such as for H. pylori bacteria associated with peptic ulcers.


Quick Fact: Relief for Localized Discomfort

Maxigan is relevant for easing symptoms related to inflammatory or irritative states, such as the redness, swelling, and tenderness characteristic of bacterial skin infections.

Regulatory References

  1. NIH MedlinePlus Drug Information

Eligibility and Restrictions for Use

Maxigan (Clarithromycin) eligibility is strictly defined by regulatory documents based on patient characteristics and pre-existing conditions.

Eligibility Scope

Eligibility Category Regulatory Statement
Populations for whom use is contraindicated Patients must not use Maxigan if they have a known hypersensitivity to macrolide antibiotics or a history of cholestatic jaundice or hepatic dysfunction associated with prior clarithromycin use. Use is also prohibited for patients with known QT prolongation, ventricular arrhythmia, or significant electrolyte disturbances (e.g., hypokalemia).
Age-related eligibility rules Maxigan is approved for adults and adolescents, and children 6 months (often as an oral suspension). Safety and efficacy have not been established in infants younger than 6 months. Older adults require caution due to the higher prevalence of underlying renal or cardiac conditions.
Condition-specific eligibility rules Use is restricted in patients with severe renal impairment (CrCl < 30 mL/min), which necessitates adjustment. Caution is required for patients with Myasthenia Gravis due to the potential for symptom exacerbation.
Pregnancy and lactation eligibility status Use during pregnancy is not recommended and should be avoided unless no appropriate alternative therapy is available. The drug is not recommended while breastfeeding as it is excreted into human milk.

Eligibility Classifications

Regulatory documents use classifications such as "Contraindicated," "Not recommended," and "Use not established" to formally define who can and cannot use the medicine.

What should I know about interactions with other medicines?

Interactions with other medicines and products

Maxigan (Clarithromycin) has officially documented interaction patterns based on its status as a strong inhibitor of Cytochrome P450 3A4 (CYP3A4) and an inhibitor of P-glycoprotein (P-gp). These dual mechanisms of pharmacokinetic exposure modification mean Maxigan significantly raises the plasma concentration of numerous co-administered drugs.

Formal Regulatory Restrictions and Prohibitions

Co-administration is formally contraindicated with several medicines due to the risk of severe, life-threatening outcomes. Prohibited combinations include: Astemizole, Pimozide, Cisapride, Terfenadine, and Domperidone (risk of cardiac arrhythmias, including Torsades de Pointes); Ergotamine and Dihydroergotamine (risk of acute ergot toxicity); and certain statins, such as Lovastatin and Simvastatin (risk of rhabdomyolysis).

Pharmacodynamic and Timing Constraints

Maxigan may cause pharmacodynamic risk reinforcement when used with other agents known to prolong the QT interval or those that affect blood glucose levels, such as oral hypoglycemic agents. Official regulatory documents state that therapy with Lovastatin or Simvastatin must be suspended during the course of Maxigan treatment. Furthermore, the Extended-Release (ER) tablets must be taken with food to ensure adequate systemic exposure, as detailed in the regulatory label.

Mechanism of Action

How Maxigan Works

Targeting the Bacterial Protein Synthesis Pathway

The action of Maxigan (Clarithromycin) is rooted in its selective interference with the protein synthesis machinery of susceptible bacteria. The core mechanism is centered on the disruption of bacterial translation. The active ingredient specifically targets the 50S ribosomal subunit, binding to the 23S ribosomal RNA (rRNA) component. This binding physically blocks the Nascent Peptide Exit Tunnel (NPET), which inhibits the ribosome's ability to process the polypeptide chain. This action leads to the cellular arrest of peptide elongation and ultimately halts the multiplication of the bacterial population.

Enhanced Mechanism via Active Metabolite

The drug's function is supported by a synergistic mechanism involving its primary breakdown product. Clarithromycin is metabolized into 14-hydroxyclarithromycin, an active compound that also possesses the ability to bind to the bacterial 50S ribosomal subunit. This metabolite enhances the parent drug’s inhibitory action, increasing the overall suppression of bacterial protein synthesis. The resultant physiological effect—the cessation of bacterial growth—results in a non-proliferating bacterial state, allowing the host's immune responses to address the microbial population.

Biological Limitations of Action

The mechanism's function can be overcome by bacterial countermeasures that constrain the drug's effect. This occurs when bacteria genetically modify the target site (the 23S rRNA), lowering Maxigan's binding affinity, or when they utilize efflux pumps to actively expel the drug from the cell. These resistance mechanisms fundamentally constrain the drug's action by preventing it from reaching or successfully engaging its molecular target.

Dosage and Administration Information

How to Use Maxigan

Maxigan (Clarithromycin) is administered based on its specific pharmaceutical formulation, which dictates both the route of administration and the dosing frequency. The medicine is available for oral use as immediate-release tablets, extended-release tablets, and oral suspension. It is also available for intravenous (IV) infusion in acute settings.

Official Dosing and Administration Patterns

The frequency of use depends on the form. Standard immediate-release tablets are typically dosed twice daily (every 12 hours), while the extended-release tablets are administered once daily. The usual adult oral doses range from 250 mg to 500 mg per dose, or 1000 mg once daily for the extended-release form. The intravenous formulation is generally limited to a maximum of five days of use, after which patients are transitioned to oral therapy.

Form Type Administration Condition Frequency Pattern
Immediate-Release Tablets/Suspension May be taken without regard to meals Twice Daily (q12h)
Extended-Release Tablets Must be taken with food and swallowed whole Once Daily (q24h)

Population-Specific Use Guidelines

Official labeling mandates specific dose modifications for certain populations to ensure proper use. For patients with severe renal impairment (creatinine clearance less than 30 mL/min), the dosage must be reduced by half. The Maxigan oral suspension is dosed in pediatric patients based on body weight, using a calculation of 15 mg/kg per day divided into twice-daily administrations for a typical course duration of 7 to 14 days.

Recent Clinical Evidence

Research Evidence for Maxigan / Overview of Studies

Research Evidence for Maxigan in Respiratory and Ear Infections

This section summarizes the types of high-quality research, such as randomized controlled trials (RCTs) and systematic reviews, that have investigated Maxigan’s study in common infections of the lower respiratory tract and middle ear. This research examines how Maxigan was studied during periods of increased symptom activity related to these conditions.

Studies on Lower Respiratory Tract Infections

Maxigan was studied for use in conditions characterized by fluctuating or episodic manifestations, such as Community-Acquired Pneumonia (CAP) and acute flare-ups of Chronic Bronchitis. Studies monitored outcomes related to physical discomfort, such as measurements of clinical outcomes and how symptoms evolved in the observed populations during the acute illness phase. Reported measured results were described in relation to those of other studied treatments. Research acknowledges that a key limitation is the lack of long-term data regarding post-treatment outcomes following the short course of treatment.


Evidence Base for Skin, Throat, and Digestive Tract Infections

Maxigan was evaluated in short-term clinical trials for acute or disruptive episodes, including infections of the throat (pharyngitis/tonsillitis), uncomplicated skin and soft tissues, and its study as a component of multi-drug regimens for the clearance of H. pylori bacteria associated with peptic ulcers. In these contexts, research monitored outcomes linked to inflammatory or irritative states.

For pharyngitis and tonsillitis, studies explored Maxigan's use in populations with known sensitivities to penicillin. Data show patterns related to measured outcomes when the local bacteria are susceptible to Maxigan. However, studies acknowledge that treatment success can be heavily influenced by increasing rates of bacterial resistance.


Long-Term Studies and Extended Follow-up

Most primary clinical research focuses on short-term outcomes related to treating the acute infection. An area of research that has generated scientific discussion concerns a specific long-term study that tracked survival patterns years after patients with stable coronary heart disease received a short course of Maxigan. The findings were mixed and inconsistent; the certainty remains low, and research is ongoing to fully establish the clinical relevance of this observed long-term association.

Key Studies & References Label: CLARITHROMYCIN tablet, film coated - NIH DailyMed

Frequently Asked Questions (FAQ)

Common questions about Maxigan (FAQ)


Q: What foods or drinks should be avoided while taking Maxigan?

Official product information specifies that the extended-release form of the medicine must be taken with food to ensure it is absorbed correctly. The immediate-release form can be taken without regard to meals. Generally, no specific common foods or beverages are listed as strictly prohibited in official labeling.


Q: What are the long-term safety concerns with Maxigan?

Regulatory reviews note that a study of patients with coronary heart disease who received a short course of the drug observed a potential increased risk of heart problems or death years after the treatment course was completed. This information is derived from a study that specifically tracked patients with underlying heart conditions.


Q: How long do I need to take Maxigan?

The total duration of use for Maxigan depends on the infection being treated, as determined by the prescriber. According to official adult oral dosing regimens for common uses, the treatment typically lasts 7 to 14 days. Use of the intravenous form is generally limited to a maximum of five days.


Q: Are there any specific safety warnings for people with heart conditions?

Official regulatory documents contain warnings for use in patients with heart disease due to the potential for increased long-term cardiac risk observed in some studies. The medicine is also contraindicated in patients with certain cardiac conditions, such as known QT prolongation.


Q: Can Maxigan be split or crushed?

Regulatory instructions for the extended-release tablets state that they must be swallowed whole. Breaking or crushing this form of the tablet is inconsistent with the required administration instructions. If you are using the immediate-release tablet form, you should refer to the specific administration instructions in the official product information.


Q: How does Maxigan affect the immune system?

The medicine's most significant regulatory-defined safety risk related to the blood and immune system is agranulocytosis. This is a rare, severe decrease in certain white blood cells that can occur during or after treatment.


Q: How long does Maxigan usually take to start working?

While the exact onset of action is not typically stated in patient-facing labels, clinical studies of Maxigan show measured effects on symptoms and infections occurring over the course of the short treatment period, which is commonly 7 to 14 days.


Q: Can Maxigan be taken with over-the-counter pain relievers?

The drug is known to interact with many medicines through the CYP3A4 pathway (a system in the liver that breaks down drugs). Due to the potential for interactions, professional review is necessary to determine use with any specific over-the-counter pain reliever.


Q: What happens if I forget to take a dose of Maxigan?

Official instructions describe taking the missed dose as soon as it is remembered. However, if it is almost time for your next scheduled dose, the missed dose should be skipped. Regulatory documents state that taking a double or extra dose to make up for a missed one is not to be done.


Q: Does Maxigan interact with birth control pills?

Regulatory documents indicate that the drug may alter the levels of hormones in oral contraceptives (birth control pills). This interaction could potentially reduce the effectiveness of birth control or increase the risk of side effects.


Q: Is there a generic version of Maxigan available?

Yes, Maxigan (Clarithromycin) is available as a generic medication in addition to its branded formulations, as stated in drug regulatory resources. The availability of generic versions is documented in regulatory databases and product resources.


Q: Does Maxigan require any special monitoring or blood tests?

Due to the rare but serious risks documented, such as blood disorders and liver injury, official labeling contains warnings for these conditions. These warnings relate to conditions that often require monitoring in a clinical setting.


Q: What if I'm taking herbal supplements, can I still use Maxigan?

Because Maxigan interacts with the body's primary drug metabolic system (CYP3A4), regulatory guidance indicates that professional review is necessary to determine use with herbal remedies or supplements.


Q: What is the typical time frame for seeing the full benefit of Maxigan?

The full benefit is typically observed during and immediately after the short course of treatment, which is commonly 7 to 14 days, as defined in clinical trial protocols.


Q: Is it safe to drink alcohol in moderation while using Maxigan?

Official information generally indicates that alcohol does not typically reduce the effectiveness of this antibiotic. Individualized guidance based on health status is available from a healthcare provider.


Q: Does Maxigan interact with common allergy medications?

Official documents list specific allergy medicines, such as Astemizole, as being formally contraindicated (prohibited) for use with Maxigan due to the risk of serious cardiac arrhythmias (irregular heartbeats).


Q: What happens if I suddenly stop taking Maxigan?

Official guidance emphasizes the importance of completing the full course of the medicine as prescribed, even if symptoms begin to improve. Stopping the medicine early may risk the infection returning.


Q: Does Maxigan interact with high blood pressure medicines?

The drug is known to interact with certain heart-related medicines (such as Digoxin) and may affect the heart's electrical activity. Reviewing the full list of interactions with a healthcare provider is necessary to assess potential risks with any specific high blood pressure medicine.


Q: Is Maxigan a prescription-only medicine?

Maxigan (Clarithromycin) is classified as a prescription-only medicine (Rx-only) in major regulatory regions.


Q: Can Maxigan be used alongside vitamins and mineral supplements?

Due to the drug's interaction profile with the body's metabolic system (CYP3A4), regulatory guidance indicates that professional review is necessary to determine use with vitamins and mineral supplements.

How should Maxigan be stored and disposed of?

How to Store and Dispose of Maxigan (Clarithromycin)

Maxigan tablets must be stored at controlled room temperature, specifically 20 C to 25 C (68 F to 77 F). The tablets require protection from light and moisture and must be kept in the original container, tightly closed.

For the oral suspension, the reconstituted liquid must be stored between 15 C and 30 C and must not be refrigerated or frozen. The suspension is stable for 14 days after mixing, after which any unused portion must be discarded.

Maxigan must be kept out of the sight and reach of children. Unused or expired medicine should not be disposed of in wastewater or household trash but must be discarded according to local regulatory requirements.

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

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