Fluticason Aurobindo

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Medically reviewed

Rosario Oropesa

Last updated on 22/12/2025

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 Fluticason Aurobindo

Property Description
Active ingredient Fluticasone Propionate
Pharmacological class Corticosteroid / Glucocorticoid
Common form Aqueous Suspension (Nasal Spray), Cream, Ointment
General purpose Anti-inflammatory and anti-allergic action
Origin Synthetic fluorinated compound

Fluticason Aurobindo: Identity and Classification

Fluticason Aurobindo is a medicinal product distinguished by its sole active substance, Fluticasone Propionate, a potent, synthetic fluorinated compound manufactured by Aurobindo Pharma. This ingredient is assigned to the pharmacological class of Corticosteroids. More specifically, it functions as a Glucocorticoid, meaning its action is to mimic the natural hormones produced by the body to help regulate inflammation. The formulation is often positioned as a prescription-only (Rx) medication, offering a focused pharmaceutical solution.

The classification as a glucocorticoid signifies that its therapeutic foundation lies in its ability to powerfully suppress the body's inflammatory and allergic responses at the cellular level. This synthetic variant is designed for high efficacy and low systemic absorption when applied locally, a critical feature for its role in anti-inflammatory therapy.

Composition, Forms, and General Therapeutic Benefit

The composition of Fluticason Aurobindo is based entirely on the efficacy of Fluticasone Propionate, which is prepared into delivery systems suited for localized action. This includes formulations such as an aqueous suspension typically used for intranasal application, or a cream and ointment base designated for topical use on the skin. The availability of these distinct dosage forms ensures that the medication can be administered directly to the site requiring treatment—such as the nasal lining or dermatological surface.

The primary general benefit of this medication is its strong anti-inflammatory activity, which serves to calm irritated tissues. The drug’s purpose is to effectively reduce physical manifestations like swelling, redness, and irritation, leading to localized relief for conditions requiring targeted anti-inflammatory support. This fundamental suppressive mechanism is the core function of the drug, irrespective of its specific route of administration.

What side effects are possible with Fluticason Aurobindo?

Possible Side Effects and Safety Information

This section summarizes the adverse reactions and safety considerations for Fluticason Aurobindo (fluticasone propionate) as documented in official government regulatory information.

Adverse Reactions Classified by Frequency

Regulatory documents categorize possible side effects based on how often they have been reported:

  • Common (ge 1/100 to <1/10): Includes epistaxis (nosebleeds), headache, nasal irritation or burning, and pharyngitis (sore throat). Localized infection with Candida albicans (thrush) in the nose or throat is also a common occurrence.
  • Rare (>1/10,000 to <1/1,000): Includes hypersensitivity reactions such as angioedema, bronchospasm, urticaria (hives), and rash.
  • Very Rare (<1/10,000): Includes serious ocular events such as glaucoma and cataracts (especially with prolonged use), and nasal septal perforation (a hole in the partition inside the nose).

Clinically Significant Safety Information

Due to its classification as a corticosteroid, the medicine carries potential systemic risks, particularly with high doses or extended use:

  • Systemic Effects: The potential for adrenal suppression (impaired adrenal function) and hypercorticism (symptoms of excess corticosteroid) exists, requiring caution, particularly in susceptible individuals.
  • Infection Risk: The drug's immunosuppressive properties mean that it should be used with caution in patients with active or inactive tuberculosis or untreated local infections, as it may worsen existing conditions or mask symptoms. Patients without immunity to measles or chickenpox should avoid exposure while using this medicine.
  • Ocular Safety: The risk of developing glaucoma or cataracts is a known long-term safety concern that requires periodic monitoring.
  • Drug Interactions: Co-administration with strong inhibitors of the Cytochrome P450 3A4 enzyme (certain medications) is generally not recommended, as this can significantly increase the drug's systemic concentration and the risk of corticosteroid side effects.
  • Pediatric Safety: The potential for growth velocity reduction in children is a documented safety consideration that necessitates regular monitoring of growth when used in the pediatric population.

Overdose and Emergency Response

Overdose and When to Seek Help

Official regulatory information emphasizes that the primary risk associated with Fluticason propionate nasal spray overdose is related to chronic misuse rather than a single acute event. Due to the drug's low systemic absorption via the nasal route, acute overdose from a large number of actuations over a short period (a few days) is generally considered unlikely to cause immediate problems and may only require observation.

Overdose Risks and Presentations

Overdose Scenario Potential Manifestation Emergency Action
Acute Overdose (Short-term, high dose) Hypercorticism is the most likely acute presentation, though usually mild. Generally requires observation only; contact health professional.
Chronic Overdose (Prolonged use above recommended dose) Adrenal suppression, potentially clinically significant. Signs of hypercorticism. Dosage should be reduced gradually under medical guidance.

When to Seek Immediate Medical Help

It is officially recommended that if you suspect you have taken too much Fluticasone Propionate, you should contact a healthcare professional, hospital emergency department, or regional Poison Control Centre immediately, even if there are no symptoms.

This immediate action is crucial because while acute effects are often minor, the most significant documented risk—adrenal suppression—is associated with prolonged excessive use and requires professional management, including a gradual reduction of the dosage. Susceptible individuals may experience systemic corticosteroid effects even at recommended dosages.

Therapeutic Uses of Fluticason Aurobindo

Fluticason Aurobindo (Fluticasone Propionate) is generally relevant for easing symptoms related to inflammatory or irritative states that drive patient discomfort across several domains. It is generally considered relevant across both respiratory and dermatological contexts where supportive symptom management is appropriate.


This medication is commonly used for managing symptoms related to inflammatory or irritative states associated with Seasonal and Perennial Allergic Rhinitis, Atopic Dermatitis (Eczema), Psoriasis, and conditions involving inflammatory or irritative processes, such as Chronic Rhinosinusitis. It is applied during phases when symptoms become more noticeable, particularly when they interfere with daily comfort. The medication helps address symptom clusters that may become intense or disruptive, such as persistent nasal congestion, excessive runny nose, continuous sneezing, and severe itching (pruritus).

“The medication is generally utilized when symptoms become more noticeable or when short-term symptomatic assistance is needed.”

This supportive therapeutic benefit provides support that helps ease the overall symptom burden and contributes to easing the overall symptom load during periods of heightened discomfort.

Quick Fact: Relief for Itching (Pruritus) and Nasal Congestion

Eligibility and Restrictions for Use

Eligibility Profile: Official Regulatory Information

This section outlines who can and cannot use Fluticasone Propionate (the active ingredient in Fluticason Aurobindo), based strictly on contraindications and precautions documented in government regulatory sources (e.g., FDA, EMA).

Classification Eligibility Rule
Absolute Contraindication Patients with a known hypersensitivity or allergy to Fluticasone Propionate or any of the inactive ingredients must not use this medicine.
Age Restriction Not recommended for children younger than 4 years of age due to insufficient data on safety and efficacy in this group. Eligibility rules vary for older children and adolescents depending on the specific product formulation (prescription vs. over-the-counter).
Conditional Avoidance Use is generally avoided or prohibited until healing is complete in the presence of recent nasal ulcers, nasal surgery, or nasal trauma.
Use with Caution Special medical consideration is required for patients with active or quiescent infections such as tuberculosis or systemic viral, fungal, or bacterial infections. Caution is also advised for those with a history of glaucoma/cataracts or severe hepatic impairment.

Pregnancy and Lactation: Use during pregnancy is generally avoided unless the expected benefit is considered essential and outweighs potential risks, as there is inadequate safety evidence. Use during breastfeeding requires caution, as it is unknown if the drug is excreted in human milk.

What should I know about interactions with other medicines?

Interactions with other medicines and products

Fluticason Aurobindo, as an inhaled or intranasal corticosteroid, is primarily metabolized by the cytochrome P450 enzyme system, specifically the CYP3A4 isozyme, in the liver. Concomitant use with strong inhibitors of this enzyme can significantly increase the systemic exposure to fluticasone, raising the risk of systemic corticosteroid side effects such as adrenal suppression and Cushing's syndrome. Therefore, it is essential to inform your healthcare provider about all medicines you are taking.

Major Interactions

  • Potent CYP3A4 Inhibitors: Coadministration with certain strong inhibitors is generally not recommended unless the potential benefit significantly outweighs the risk. These include some medications used to treat HIV or viral infections (e.g., ritonavir, cobicistat) and certain antifungal medications (e.g., ketoconazole, itraconazole).

  • Other Corticosteroids: Combining this medicine with other systemic or locally applied corticosteroids (e.g., steroid tablets, injections, or other asthma/eczema treatments) may increase the overall steroid load on the body and should be closely monitored by a healthcare professional.

Other Considerations

  • Moderate CYP3A4 Inhibitors: While the risk is generally lower than with potent inhibitors, moderate inhibitors may also increase fluticasone levels. Your doctor may need to monitor you for signs of increased steroid effect.
  • Grapefruit Juice: Ingesting large quantities of grapefruit juice can inhibit CYP3A4 and potentially increase systemic fluticasone exposure. You should consult your doctor or pharmacist about consuming grapefruit products while on this treatment.

Always provide your doctor with a complete list of all prescription, over-the-counter, and herbal remedies you are using before starting Fluticason Aurobindo.

Mechanism of Action

Fluticason (as fluticasone propionate) functions as a synthetic agonist with high selective affinity for the intracellular Glucocorticoid Receptor (GR), a ligand-activated transcription factor found in target cells such as mast cells, eosinophils, and lymphocytes.

Upon binding, the drug-receptor complex undergoes nuclear translocation and modulates gene expression through two primary mechanisms: transactivation and transrepression.

Via transactivation, the complex binds to Glucocorticoid Response Elements (GREs) on the DNA to upregulate the transcription of anti-inflammatory proteins, such as annexin-1. Concurrently, transrepression, considered the primary anti-inflammatory mechanism, occurs as the complex directly interacts with and inhibits the activity of pro-inflammatory transcription factors, including Nuclear Factor-kappa B (NF-κB) and Activator Protein-1 (AP-1).

This molecular inhibition suppresses the transcription and subsequent release of numerous pro-inflammatory mediators, including cytokines (e.g., IL-1, TNF-α), chemokines (e.g., RANTES), and eicosanoids (e.g., leukotrienes). The resulting downstream cellular consequence is the promotion of eosinophil apoptosis and a generalized reduction in inflammatory cell proliferation, resulting in system-level physiological modulation characterized by reduced tissue edema and suppressed vascular permeability.

Dosage and Administration Information

Official Administration Instructions

The medicine is administered by the intranasal route only. Regular, continuous use is essential, as the maximum therapeutic benefit may not be obtained until after several days of treatment.

Dosing Schedule and Age-Specific Rules

Age Group Recommended Starting Dose Maximum Total Daily Dose
Adults and Adolescents (ge12 yrs) 2 sprays per nostril once daily 4 sprays per nostril (400 mcg)
Children (4–11 yrs) 1 spray per nostril once daily 2 sprays per nostril (200 mcg)

Once adequate control is achieved, the dose should be reduced to the lowest effective level for maintenance therapy. The maximum total daily dose for the patient's age group must not be exceeded.

Preparation and Procedure

  1. Preparation: Gently shake the bottle before each use. The nasal spray pump must be primed (test sprays released into the air away from the face) before the first use, or if the product has not been used for one week or more, until a fine mist appears.
  2. Administration: Insert the nasal tip into one nostril while holding the other closed. The patient must breathe in gently through the nostril while actuating the spray.
  3. Missed Dose: If a dose is missed, the patient should take the next dose at the usual scheduled time; do not take a double dose to make up for the missed one.

Recent Clinical Evidence

Fluticason Aurobindo: Recent Clinical Evidence

Summary of Clinical Trials

Studies have explored the use of Fluticason Aurobindo for chronic inflammatory conditions, with research examining its potential association with changes in symptoms and quality of life. The clinical trials typically evaluated its application via inhalation or nasal spray across various dose levels.

Research has investigated whether the drug is associated with reduced symptom severity over specific treatment periods. Studies compared outcomes, including the frequency of exacerbations and patient-reported symptoms, between the drug and placebo groups. The overall findings often focus on how the drug's properties may affect inflammatory processes in the airways or nasal passages.


Outcomes and Research Focus

In research, the study hypothesis explored the drug's role in influencing inflammatory markers. Studies evaluated the drug's association with primary endpoints such as Forced Expiratory Volume in 1 second (FEV1) in pulmonary studies or Nasal Symptom Scores in rhinitis studies.

The primary focus of many studies was the evaluation of changes in disease activity scores after a specified duration of treatment. Some research also explored participant-reported outcomes related to daily function and overall well-being.


Safety and Tolerability Research

Studies examined potential interactions with other common medications to evaluate changes in safety profiles. Research sought to identify whether co-administration was associated with an increased incidence of adverse events or altered drug concentrations, particularly with cytochrome P450 inhibitors.

Studies also evaluated the use of the drug in specific populations, such as pediatric and older adult participants, to examine any potential differences in safety and tolerability profiles. Research has also examined the bioavailability of the formulation compared to previously studied versions. The research included comprehensive reporting on the spectrum of observed adverse events.

Frequently Asked Questions (FAQ)

Common questions about Fluticason Aurobindo (FAQ)

Q: What is the active ingredient in Fluticason Aurobindo?

The active ingredient in Fluticason Aurobindo is fluticasone propionate. This is a type of corticosteroid, and according to official product information, it is intended to help relieve inflammation in the affected areas.

Q: What is Fluticason Aurobindo used for?

Regulatory documents state that Fluticason Aurobindo is used to treat conditions caused by inflammation (swelling and irritation) and allergic reactions. It is prescribed for certain skin and scalp conditions, as well as specific nose and eye problems.

Q: Does Fluticason Aurobindo contain alcohol?

Yes, some formulations of Fluticason Aurobindo, such as the cream, contain cetostearyl alcohol as an inactive ingredient. This information is noted in the official product documents.

Q: Can I use Fluticason Aurobindo if I have a fungal infection?

According to the official product information, Fluticason Aurobindo should not be used if you have an untreated infection of the skin, such as a fungal infection (like athlete's foot or candidiasis), or a bacterial or viral infection. If you have an infection, official guidance indicates it should be treated simultaneously with or before using this medicine.

Q: Is Fluticason Aurobindo safe to use near the eyes?

Official labeling advises that special care should be taken when using this medicine near the eyes. Official documents warn against getting Fluticason Aurobindo into the eyes, as prolonged exposure may lead to vision problems like cataracts or glaucoma (increased pressure in the eye).

Q: Can children use Fluticason Aurobindo?

Yes, official product information indicates that Fluticason Aurobindo can be used by children, but generally for shorter durations and with smaller amounts compared to adults. The suitability and exact instructions for use in children should be discussed with a healthcare provider.

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

Official product information generally suggests applying a forgotten dose when remembered, unless it is close to the time for the next dose, in which case the missed dose is usually skipped. Patients should follow the specific instructions provided by their healthcare professional.

Q: What should I do if I use too much Fluticason Aurobindo?

According to the regulatory documents, using too much of this medicine for a short period is generally not harmful. However, if it has been used too often or for too long, it can potentially lead to side effects. If you have concerns about overusing this medication, official guidance recommends consulting with a healthcare professional.

Q: How should Fluticason Aurobindo be stored?

Official information states that Fluticason Aurobindo should be stored below 25°C. It must be kept out of the sight and reach of children. It is important to check the original packaging for the specific expiry date and disposal instructions.

How should Fluticason Aurobindo be stored and disposed of?

How to Store and Dispose of Fluticason Aurobindo?

The storage and disposal of Fluticason Aurobindo must strictly follow the requirements defined in official government regulatory documents to ensure product stability and safety. The active ingredient, Fluticasone Propionate, is governed by specific temperature and handling mandates.

Requirement Area Official Rule
Temperature Mandate Store the nasal spray between 4 C and 30 C. Do not store topical forms above 30 C.
Child Safety The medicine must be kept out of the sight and reach of children.
Stability Limits The cream formulation must be discarded 6 months after the first time the tube is opened. The nasal spray unit must be discarded after the total specified number of sprays.
Special Handling Fabric that contacts the cream or ointment can be a serious fire hazard; avoid smoking or naked flames near the product.
Disposal Protocol Do not dispose of unused or expired medicine in household waste or wastewater. Dispose of the product strictly according to local pharmaceutical return schemes and national requirements.

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

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