Fusacid H

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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 Fusacid H

Quick Facts

Property Description
Active Ingredient Fusidic Acid and Hydrocortisone
Form Cream (Topical preparation)
Pharmacological Class Topical Antibiotic and Corticosteroid Combination
General Purpose Managing inflammatory skin conditions with concurrent bacterial infection
Origin Semi-synthetic (Fusidic Acid) and Synthetic (Hydrocortisone)

What Type of Medicine is Fusacid H?

Fusacid H is defined as a combination product for topical administration, formally classified in the pharmacological class of Hydrocortisone and Antibiotics (ATC code D07CA01). This medicinal entity is typically supplied as a cream, distinguishing it as a dual-action agent that delivers two separate active compounds simultaneously to the skin surface. As a dual-component product, it is fundamentally distinct from monotherapy treatments, reflecting its capacity to address both bacterial involvement and inflammation concurrently.

Understanding the Dual Active Ingredients and Origin

The formulation's efficacy relies on the synergy between its two active ingredients: the antibiotic Fusidic Acid and the mild corticosteroid Hydrocortisone. Fusidic Acid is derived semi-synthetically from the fungus Fusidium coccineum and is primarily utilized for its antibacterial action against susceptible organisms. Hydrocortisone, a synthetic glucocorticoid, provides the essential anti-inflammatory effect. The combination of these agents has been clinically recognized for treating infected eczematous dermatitis. This establishes the medicine as suitable for addressing the complex challenge of skin inflammation compounded by a bacterial presence.

General Purpose: Why is This Combination Used?

The general purpose of using Fusacid H is the effective, synchronized management of inflammatory skin conditions—such as localized dermatitis—that are complicated by a secondary bacterial infection. The formulation leverages the anti-inflammatory effect of Hydrocortisone to quickly mitigate patient discomfort, including common symptoms like redness and swelling, while the Fusidic Acid component addresses the microbial proliferation. This strategic dual approach provides comprehensive support by controlling the infection source while rapidly alleviating the patient's acute symptoms.

What side effects are possible with Fusacid H?

Possible side effects and safety information

The official safety profile for the topical combination of Fusidic Acid and Hydrocortisone is based on regulatory classifications of adverse reactions, primarily categorized by frequency and system-organ class.

Documented Adverse Reactions

Adverse reactions are most frequently classified as related to the administration site and skin disorders. Common adverse reactions, defined as occurring in 1 to 10 out of every 100 users, include pruritus (itching), burning sensation, and irritation at the application site. Reactions classified as Uncommon include contact dermatitis, aggravation of eczema, and rash. Serious adverse effects are known class effects of the corticosteroid component.

Key Safety Considerations

The regulatory safety profile highlights the risk of potential systemic corticosteroid class effects when the cream is applied extensively or for prolonged periods. These effects, which include HPA axis suppression (adrenal suppression) and raised intra-ocular pressure (glaucoma), are explicitly documented in official prescribing information. Paediatric patients (children) are noted to have a greater susceptibility to these systemic effects due to their higher skin surface area-to-body weight ratio.

Safety documentation also specifies that long-term use is associated with local adverse effects such as skin atrophy, striae (stretch marks), and telangiectasia. Furthermore, the label notes that the cream contains excipients like cetyl alcohol and butyl hydroxyanisole, which may cause localized contact dermatitis. Prolonged treatment may also contribute to the risk of antibiotic resistance to Fusidic Acid.

Overdose and Emergency Response

Overdose and When to Seek Help

Official regulatory information describes specific risks associated with accidental ingestion or excessive, prolonged topical use of Fusacid H, which contains a corticosteroid. The documented overdose profile focuses on the potential for systemic corticosteroid effects, rather than effects from fusidic acid.


Documented Overdose Risks

Topical application of corticosteroids in large amounts and for more than three weeks may lead to systemic effects such as Cushing's syndrome or adrenocortical insufficiency. These conditions reflect the potential for the corticosteroid component to disrupt the body's natural hormone balance.

For the fusidic acid component, no specific symptoms or signs of overdose following topical administration are known. Systemic consequences following accidental oral intake of the cream are generally considered unlikely to occur because the total amount of active substance in one tube is below the systemic daily dose used for other treatments.


Required Emergency Actions

It is mandatory to seek immediate medical attention for any suspected overdose or accidental swallowing of the cream, even if the person appears well and has no symptoms. Regulatory bodies instruct contacting a healthcare professional, hospital emergency department, or regional Poison Control Centre immediately for assessment and guidance.

Therapeutic Uses of Fusacid H

Fusacid H is commonly used in clinical settings that involve acute or unstable symptom patterns of specific skin conditions.

The cream is used for managing localized dermatitis or eczema that has become complicated by a secondary bacterial infection, playing a role in addressing this dual presentation. It is applied in situations where the skin displays symptoms related to inflammatory or irritative states, such as redness and swelling, alongside signs of secondary infection.

The primary benefit is supportive relief of distressing, acute symptoms. The medication helps to ease pronounced manifestations like intense itching (pruritus) and irritation, contributing to improved comfort during periods of heightened symptoms. This cream is commonly used in scenarios where symptoms escalate temporarily, including episodes of infected eczematous dermatitis.


Quick Fact: Relief for Dual Symptom Clusters

Property Description
Core Symptom Focus Irritative States and Signs of Secondary Infection
Relief Focus Redness, Swelling, and Intense Itching (Pruritus)
Clinical Scenarios Acute Flare-ups of Infected Eczema
Patient Benefit Supports stability and eases overall symptom burden

Regulatory References

  1. Health Canada Product Monograph

Eligibility and Restrictions for Use

Eligibility Map: Who can and cannot use Fusacid H

The eligibility for Fusacid H is defined by specific contraindications and restrictions related to its dual composition of a mild corticosteroid and an antibiotic.


Populations for whom use is Contraindicated:

The medicine must not be used by patients with a known hypersensitivity to fusidic acid, hydrocortisone acetate, or any excipient. Use is also strictly prohibited for patients with primary skin conditions caused by fungi, viruses (such as chickenpox or herpes), or tuberculosis. Furthermore, it is contraindicated for patients with rosacea, perioral dermatitis, or skin eruptions following vaccination.


Age-Related and Conditional Use Rules:

  • Children/Infants must use the cream with special caution due to an increased risk of systemic effects, such as HPA axis suppression.
  • Use is not recommended on areas like atrophic skin, cutaneous ulcers, or acne vulgaris.
  • For all patients, long-term continuous topical therapy must be avoided, with use typically limited to no more than 14 days.
  • Pregnancy and lactation require caution; while permitted if clinically needed, extensive or prolonged application is restricted, and application on the breast must be avoided while nursing.

What should I know about interactions with other medicines?

Interactions with other medicines and products

Official Regulatory Interaction Profile

The official regulatory documentation for the topical combination cream, Fusacid H (Fusidic Acid and Hydrocortisone), states that formal drug-drug interaction studies have not been performed with this specific preparation. Consequently, the interaction profile is not focused on metabolic or transporter-mediated drug interactions, as systemic absorption is generally minimal.

Documented Pharmacodynamic and Exposure Risks

While specific drug–drug interactions are not listed, the interaction map is structured around risks associated with the Hydrocortisone component. Co-administration with other medicines containing corticosteroids requires caution due to the potential for an additive systemic pharmacodynamic effect.

Interaction Type Documented Constraint
Pharmacodynamic Caution with other corticosteroids (risk of additive systemic effect).
Exposure Risk Risk of increased systemic exposure is amplified by factors like extensive application or occlusive dressings.
Population-Specific Note Pediatric patients exhibit higher susceptibility to the systemic effects of topical corticosteroids.

No interactions with food, alcohol, or herbal products are explicitly documented in the official regulatory product label. Additionally, the label does not specify any mandatory timing or separation requirements for co-administered medicinal products.

Mechanism of Action

The drug's mechanism involves two distinct, complementary molecular actions on microbial proliferation and the host's inflammatory response. The resulting physiological change is a product of the coordinated action of its two active components on distinct biological systems.


Controlling Bacterial Growth by Halting Protein Synthesis

The Fusidic Acid component exerts a bacteriostatic effect by acting directly on the microbial machinery. It targets the Bacterial Elongation Factor G (EF-G), an enzyme critical for protein chain elongation during ribosomal translation. Fusidic acid binds to and stabilizes the post-translocational ribosome complex , jamming the mechanism and preventing the next amino acid from being added. This molecular action leads to the cessation of growth and replication in susceptible bacteria.


Attenuating Inflammation via Glucocorticoid Receptor Modulation

The Hydrocortisone component is a steroid that engages the Cytoplasmic Glucocorticoid Receptors (GR) . Upon activation, the hydrocortisone-GR complex translocates into the cell nucleus, where it modulates gene transcription. This process reduces the production of pro-inflammatory mediators, such as prostaglandins and leukotrienes, by inhibiting the activity of Phospholipase A2. This mechanism leads to the suppression of the local tissue reaction, which involves reduced fluid accumulation and decreased blood vessel dilation.


Mechanistic Synergy and Causal Management

The mechanistic profile relies on the complementary action of these two separate domains. The Hydrocortisone mechanism modulates the host's inflammatory signaling, while the Fusidic Acid mechanism modulates bacterial growth. This dual influence facilitates the simultaneous cessation of microbial proliferation and attenuation of the localized inflammatory cascade.

Dosage and Administration Information

How to Use Fusacid H: Administration Guidelines

This section outlines the standardized administration and dosage guidelines for Fusacid H (Fusidic Acid and Hydrocortisone Cream).


Administration Scope

The cream is classified for Topical (cutaneous) use only.

Feature Instruction
Route of Administration Topical (External use on the skin only)
Dosing Schedule Apply a small quantity to the affected area. The amount may be estimated using the Fingertip Unit (FTU) concept.
Dosing Frequency Typically applied Twice daily (b.i.d.). Application may be less frequent if the affected area is covered by a dressing.

Constraints and Duration of Use

Standard labeling defines limits on the treatment duration and specific constraints to ensure appropriate use of the combined antibiotic and corticosteroid.

  • Treatment Duration Limit: A single course of treatment should not normally exceed 14 days (two weeks). Long-term continuous topical therapy must be avoided.
  • Administration Focus: The cream should be gently rubbed into the affected area. Users must take care to avoid contact with the eyes and mucous membranes.
  • Pediatric Use: When treating children, the dose should still be measured using an adult’s index finger to define the Fingertip Unit.
  • Handling Restriction: Clothing or bedding that has been in contact with the product is identified as a fire hazard; contact with naked flames should be avoided.

These instructions define a controlled, short-term protocol for the cream's proper application.

Recent Clinical Evidence

Research evidence / Overview of studies for Fusacid H


Evidence for Use in Infected Eczematous Dermatitis

The foundation of the research for this combination medicine is primarily based on Randomized Controlled Trials (RCTs). These studies was evaluated in research exploring how symptoms change over time in individuals with inflammatory skin conditions characterized by fluctuating or episodic manifestations—specifically, eczema or dermatitis that also involved a bacterial infection. The research examined outcomes related to physical discomfort and skin health, applying them in studies observing responses over defined time intervals.

Studies explored the treatment's effect compared to other topical applications and to non-active creams (vehicles). Researchers monitored endpoints such as Overall Clinical Success, which was studied for assessment using standardized rating systems designed to assess the severity of the skin condition. The research also examined specific symptom metrics, including patterns in local manifestations like outcomes related to redness, swelling, and itching (pruritus).

Findings describe patterns observed in the studies over the short term. Research highlights that evidence quality varies across studies, and some trials included comparison groups that received only a corticosteroid, leaving aspects of the contribution of the antibiotic component less clear.


Evidence in Special Populations: Children and Infants

The use of the combination was evaluated in specific special populations. The research includes data from pediatric populations, making the evidence relevant in trials assessing short-term or episodic symptom patterns in younger individuals. Study protocols included children, with some research enrolling infants as young as 3 months of age with clinically infected eczema.

This research, applied in studies examining patient-reported experiences in these younger age groups, contributes to the broader evidence landscape in the context of pediatric evidence. However, similar to the adult trials, the results apply only to the populations studied, and the sample sizes for particular pediatric subgroups was observed in some studies to be more modest than those for adults.


What Remains Uncertain About the Research Base

Authoritative sources note that the current evidence base describes the research conducted for acute infected eczema, but several areas remain insufficient or not fully characterized.

One key area of uncertainty is the direct comparison to corticosteroid monotherapy: research highlights that comparative evidence is lacking in some study designs, and the contribution of the fusidic acid component remains uncertain in these contexts. Furthermore, The research is ongoing regarding research gaps related to the specific topical use of the antibiotic and antibiotic resistance.

Key Studies & References

  1. National clinical guideline for the management of Eczema: Diagnosis and management of atopic eczema in primary and secondary care
  2. Drug Monograph for Fusidic Acid and Hydrocortisone Cream (Health Canada Product Monograph)

Frequently Asked Questions (FAQ)

Common questions about Fusacid H (FAQ)

Q: Why is the 'H' in Fusacid H important to know about?

A: Fusacid H is officially classified as a combination product. The 'H' is used to identify the hydrocortisone component, which is a mild corticosteroid combined with the antibiotic fusidic acid. This dual composition provides both an antibacterial action and an anti-inflammatory effect, which is the intended use defined in official documents.

Q: What is the typical length of time Fusacid H is prescribed for?

A: Official regulatory documents state that a single course of treatment should not normally be continued for more than 14 days (two weeks). This maximum limit is specified in the regulatory guidelines as a safety measure for short-term, controlled use.

Q: Can Fusacid H be applied on the face?

A: Regulatory documents advise that as with all corticosteroids, prolonged use on the face should be avoided. It is essential to take specific care to avoid contact with the eyes and mucous membranes during application. Guidance on specific application areas is provided by the healthcare professional.

Q: Can children use Fusacid H?

A: Use of this medicine in children requires special caution due to their higher susceptibility to the systemic effects of topical corticosteroids. Regulatory guidance for related products notes that continuous treatment for longer than three weeks is advised against for patients under three years of age due to the risk of adrenocortical suppression.

Q: What is the chance of getting a systemic side effect from topical Fusacid H?

A: The potential for systemic side effects, such as HPA axis suppression (adrenal gland suppression), exists when the cream is applied extensively or for prolonged periods. However, official documentation does not provide an incidence rate or frequency for these effects under normal, short-term use.

Q: Is it possible to become resistant to the antibiotic in Fusacid H?

A: Official regulatory documents report that bacterial resistance has been known to occur with the topical use of fusidic acid. The risk of resistance development is addressed by the regulatory requirement to limit treatment duration to no more than 14 days.

Q: What should I do if I forget a time to apply Fusacid H?

A: According to official patient information, if an application is missed, it can be applied as soon as remembered. However, if it is near the time for the next scheduled dose, the missed dose should be skipped, and the regular schedule is continued. Doubling a dose is advised against.

Q: Can Fusacid H be used to treat eczema that has become infected?

A: Yes, the medicine is officially indicated for the treatment of inflammatory skin conditions, such as eczema or dermatitis, that are complicated by a secondary bacterial infection.

Q: What is the difference between Fusacid and Fusacid H?

A: The key difference lies in the composition. Fusacid H is a combination product containing two active ingredients: fusidic acid and the steroid hydrocortisone. Fusacid (without the ‘H’) typically contains only the antibiotic fusidic acid as the single active ingredient.

Q: Can Fusacid H be used for fungal infections?

A: No. Due to the presence of the corticosteroid component, the medicine is contraindicated (must not be used) for primary skin conditions caused by fungi or viruses. The product is indicated for the management of inflammatory skin conditions complicated by bacterial infection.

Q: Does Fusacid H sting or burn when it's applied?

A: A burning sensation at the application site is a documented common adverse reaction, defined in regulatory documents as occurring in 1 to 10 out of every 100 users.

Q: Is there a rebound effect if I stop using Fusacid H suddenly?

A: Regulatory warnings indicate that rebound flares after stopping treatment, sometimes referred to as topical steroid withdrawal syndrome, are possible. This potential is noted in regulatory warnings, particularly when topical steroids are used for prolonged periods.

Q: What if I accidentally put Fusacid H in my eye?

A: Official guidance advises that contact with the eyes must be avoided. If accidental contact occurs, rinsing the eye immediately with water is noted. Prolonged exposure is associated with the risk of irritation and possible serious side effects such as glaucoma.

Q: Can Fusacid H change my skin color (cause pigmentation changes)?

A: Official documentation notes that use of this medication for prolonged or repeated periods may result in skin discoloration. This is a recognized local effect associated with long-term use of corticosteroids.

Q: Is Fusacid H safe to use on delicate areas like skin folds?

A: Regulatory warnings indicate that absorption of the corticosteroid into the bloodstream is promoted when the cream is applied in skin folds (flexures). This enhanced absorption increases the risk of systemic effects.

Q: What does it mean if my rash looks worse after using Fusacid H for a few days?

A: A worsening rash may be an uncommon adverse reaction, such as an aggravation of eczema, which is noted in regulatory safety information. It may also indicate that the infection is not responding to treatment. A worsening condition is typically reviewed by a healthcare professional.

Q: Is there a specific age limit for who can use Fusacid H?

A: The specific restriction related to age is that continuous treatment for longer than three weeks is advised against in patients under the age of three years. This is due to the potential risk of adrenocortical suppression in infants and young children.

Q: Can Fusacid H affect the results of allergy skin tests?

A: Topical steroids, such as the hydrocortisone component in this medicine, may interfere with the accuracy of allergy skin test results. They are sometimes advised to be temporarily discontinued for a period before testing to ensure reliable results.

Q: Can I apply makeup or lotion over Fusacid H?

A: Regulatory documents warn that using dressings or covering the treated area can increase the risk of systemic exposure to the hydrocortisone component. Regulatory caution regarding occlusive dressings suggests that heavy applications of other topical products could similarly increase the potential for systemic exposure.

Q: Does Fusacid H interact with common acne medications?

A: Official regulatory documentation states that formal drug-drug interaction studies have not been performed for this specific combination product. Users seeking co-administration guidance are advised to review their complete treatment plan with a healthcare professional.

Q: Is it safe to use Fusacid H with other topical steroid creams?

A: Regulatory documents state that co-administration with other medicines containing corticosteroids requires caution. This is due to the potential for an additive systemic effect from the hydrocortisone component.

Q: Does Fusacid H interact with oral antibiotics?

A: Since the medicine is for topical use, systemic interactions are generally considered unlikely due to minimal systemic absorption into the bloodstream. No interactions with oral antibiotics are explicitly documented in the official regulatory product label.

Q: Can Fusacid H be used on open wounds or broken skin?

A: Official guidance states that contact with open wounds and mucous membranes should be avoided during application. This restriction is in place to minimize the risk of increased absorption and potential side effects.

Q: Are there any food or drink interactions with Fusacid H?

A: The official regulatory product label for this topical cream does not explicitly document any known interactions with food, alcohol, or herbal products.

Q: Can people with liver or kidney issues use Fusacid H?

A: Regulatory documents for the base fusidic acid component indicate that no specific risks or special precautions for patients with hepatic (liver) or renal (kidney) impairment have been identified. The topical route results in minimal systemic exposure.

Q: Is Fusacid H safe for elderly patients?

A: Regulatory documents for the base fusidic acid component indicate that no specific risks or special precautions have been identified for elderly patients. It is applied topically, which results in minimal absorption into the systemic circulation.

How should Fusacid H be stored and disposed of?

How to Store and Dispose of Fusacid H: Official Requirements

Storage and Stability

Fusacid H cream must be stored strictly out of the sight and reach of children. The product should be kept at a controlled room temperature, typically below 30°C or not above 25°C, and protected from excessive heat, light, and dampness. After the tube is first opened, the medicine has a limited in-use shelf-life and must be discarded within a specific period, usually three months (or four weeks), even if unused product remains.

Disposal Instructions

Expired or unused Fusacid H must not be disposed of in household trash or poured down a drain/toilet. To ensure proper pharmaceutical waste handling and environmental protection, patients must ask a pharmacist how to discard the medicine they no longer need.

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

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