Flovent for Dogs & Cats - HFA 220 mcg - [Asthma Treatment] | On Sale | EntirelyPets Rx
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Flovent for Dogs & Cats - HFA 220 mcg - [Asthma Treatment]

Flovent for Dogs & Cats - HFA 220 mcg - [Asthma Treatment]

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Description

Flovent HFA is used to treat asthma and helps to prevent symptoms of asthma. Flovent HFA contains a medicine called fluticasone propionate, which is a synthetic corticosteriod. Corticosteroids are nautral substances found in the body to help fight inflammation. Flovent helps reduce airway inflammation, an underlying cause of asthma symptoms.

Key Benefits

  • Treats chronic bronchitis in dogs and cats and chronic feline asthma and sinusitis
  • Flovent has no demonstrated side effects
  • Most effective when used with the AeroKat or AeroDawg Aerosol Chambers

Flovent HFA (fluticasone) is an inhaled aerosol steroid that is proven effective in humans, as well as cats and dogs suffering from chronic asthma or bronchitis. Your veterinarian can choose from three different strengths of Flovent for your pet. A built-in dose counter on the canister makes it easy to track the number of doses left. Using special feline and canine aerosol masks (sold separately) helps ensure that your pet receives the full dose of Flovent.

How It Works

Flovent helps reduce swelling and irritation in the airways of the lung so your dog or cat can breathe easier. The active ingredient in Flovent HFA (Fluticasone) is a corticosteroid that’s proven to reduce inflammation, a major cause of constricted, difficult breathing.

Indications

  • Maintenance treatment of asthma as prophylactic therapy in patients
  • Teatment of asthma in patients requiring oral corticosteroid therapy.
  • Not indicated for the relief of acute bronchospasm

Directions

View Floven HFA Drug Facts Sheet.

FLOVENT HFA should be administered by the orally inhaled route only in patients aged 4 years and older. After inhalation, the patient should rinse his/her mouth with water without swallowing to help reduce the risk of oropharyngeal candidiasis.

Individual patients will experience a variable time to onset and degree of symptom relief. Maximum benefit may not be achieved for 1 to 2 weeks or longer after starting treatment.

After asthma stability has been achieved, it is always desirable to titrate to the lowest effective dosage to reduce the possibility of side effects. For patients who do not respond adequately to the starting dosage after 2 weeks of therapy, higher dosages may provide additional asthma control. The safety and efficacy of FLOVENT HFA when administered in excess of recommended dosages have not been established.

The recommended starting dosage and the highest recommended dosage of FLOVENT HFA, based on prior asthma therapy, are listed in Table 1.

Recommended Dosages of FLOVENT HFA Inhalation Aerosol

NOTE: In all patients, it is desirable to titrate to the lowest effective dosage once asthma stability is achieved.

Previous Therapy Recommended Starting Dosage Highest Recommended Dosage
Adult and adolescent patients (aged 12 yearsand older)
Bronchodilators alone 88 mcg twice daily 440 mcg twice daily
Inhaled corticosteroids 88-220 mcg twice dailya 440 mcg twice daily
Oral corticosteroidsb 440 mcg twice daily 880 mcg twice daily
Pediatric patients (aged 4-11 years)c 88 mcg twice daily 88 mcg twice daily

a Starting dosages above 88 mcg twice daily may be considered for patients with poorer asthma control or those who have previously required doses of inhaled corticosteroids that are in the higher range for the specific agent.

b For patients currently receiving chronic oral corticosteroid therapy, prednisone should be reduced no faster than 2.5 to 5 mg/day on a weekly basis beginning after at least 1 week of therapy with FLOVENT HFA. Patients should be carefully monitored for signs of asthma instability, including serial objective measures of airflow, and for signs of adrenal insufficiency [see Warnings and Precautions (5.4)]. Once prednisone reduction is complete, the dosage of FLOVENT HFA should be reduced to the lowest effective dosage.

c Recommended pediatric dosage is 88 mcg twice daily regardless of prior therapy. A valved holding chamber and mask may be used to deliver FLOVENT HFA to young patients.

Prime FLOVENT HFA before using for the first time by releasing 4 sprays into the air away from the face, shaking well for 5 seconds before each spray. In cases where the inhaler has not been used for more than 7 days or when it has been dropped, prime the inhaler again by shaking well for 5 seconds and releasing 1 spray into the air away from the face.

Dosage forms and Strengths

Inhalation Aerosol. Dark orange plastic inhaler with a peach strapcap containing a pressurized metered-dose aerosol canister containing 120 metered inhalations and fitted with a counter. Each actuation delivers 44, 110, or 220 mcg of fluticasone propionate from the mouthpiece.

Cautions

Keep out of reach of children and pets. Store at room temperature. Shake product well before use.

Contraindications

  • Primary treatment of status asthmaticus or acute episodes of asthma requiring intensive measures.
  • Hypersensitivity to any ingredient.

Warnings & Precautions

  • Candida albicans infection of the mouth and pharynx may occur. Monitor patients periodically. Advise the patient to rinse his/her mouth with water without swallowing after inhalation to help reduce the risk.
  • Potential worsening of infections (e.g., existing tuberculosis; fungal, bacterial, viral, or parasitic infection; ocular herpes simplex). Use with caution in patients with these infections. More serious or even fatal course of chickenpox or measles can occur in susceptible patients.
  • Risk of impaired adrenal function when transferring from systemic corticosteroids. Taper patients slowly from systemic corticosteroids if transferring to FLOVENT HFA.
  • Hypercorticism and adrenal suppression may occur with very high dosages or at the regular dosage in susceptible individuals. If such changes occur, discontinue FLOVENT HFA slowly.
  • Assess for decrease in bone mineral density initially and periodically thereafter.
  • Monitor growth of pediatric patients.
  • Close monitoring for glaucoma and cataracts is warranted.

Adverse Reactions

Most common adverse reactions (incidence greater than 3%) are upper respiratory tract infection or inflammation, throat irritation, sinusitis, dysphonia, candidiasis, cough, bronchitis, and headache.

To report SUSPECTED ADVERSE REACTIONS, contact GlaxoSmithKline at 1-888-825-5249 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

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