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Prescribing Information
NICOTROL® Inhaler (nicotine inhalation system)
10 mg per cartridge (4 mg delivered)
How Supplied
Return to the NICOTROL Inhaler Product Center

NICOTROL INHALER (nicotine inhalation system) is supplied as 168 cartridges each containing 10 mg (4 mg is delivered) nicotine (NDC 0009-5400-01). Each unit consists of 5 mouthpieces, 28 storage trays each containing 6 cartridges and 1 plastic storage case. A patient information leaflet is enclosed with the package.

Store at room temperature not to exceed 77°F (25°C).
Protect cartridges from light.

Rx only

LAB-0345-3.0
Revised December 2008


NICOTROL Safety Information
 

NICOTROL® Inhaler (nicotine inhalation system) 10 mg per cartridge (4 mg delivered)

NICOTROL Inhaler (nicotine inhalation system) is indicated as an aid to smoking cessation for the relief of nicotine withdrawal symptoms. NICOTROL Inhaler therapy is recommended for use as part of a comprehensive behavioral smoking cessation program.

Important Safety Information

NICOTROL Inhaler therapy is contraindicated in patients with known hypersensitivity or allergy to nicotine, menthol or to any component of the product.

The safety and efficacy of the continued use of NICOTROL Inhaler for periods longer than 6 months have not been adequately studied and such use is not recommended.

The patient must stop smoking completely before using the NICOTROL Inhaler.

Because nicotine is addictive, patient dependency upon the NICOTROL Inhaler is possible. It is important the patient use it only for as long as needed to overcome a smoking habit.

Prior to starting NICOTROL Inhaler, the patient must inform the healthcare professional of all medications he or she is taking. Certain concomitant medications may require a dosage adjustment.

A special note about children and pets. The NICOTROL Inhaler can cause serious illness in children and pets—even in very small amounts. If a child chews on or swallows NICOTROL Inhaler cartridges, immediately call a doctor or call your regional poison center.

Adverse events. In clinical trials NICOTROL Inhaler was associated with local irritant side effects of the mouth and throat. The most common nicotine-related adverse event reported by patients on active drug was dyspepsia. Other nicotine-related events present in greater than 3% of patients on active drug included nausea, diarrhea, and hiccup. Smoking-related adverse events present in greater than 3% of patients on active drug included chest discomfort, bronchitis, and hypertension.

Adverse events of unknown relationship to nicotine occurring in greater than 3% of patients on active drug included headache, influenza-like symptoms, pain, back-pain, allergy, paresthesias, flatulence, and fever.

Pregnancy and nursing. The specific effects of NICOTROL Inhaler treatment on fetal development and nursing infants are unknown. Therefore, pregnant and nursing smokers should be encouraged to attempt cessation using educational and behavioral interventions before using pharmacological approaches.

Bronchospastic disease. The NICOTROL Inhaler has not been specifically studied in asthma or chronic pulmonary disease. Therefore, the NICOTROL Inhaler should be used with caution in patients with bronchospastic disease because nicotine is an airway irritant and might cause bronchospasm.

Cardiovascular and peripheral vascular diseases. The NICOTROL Inhaler should be used with caution in patients with cardiovascular and peripheral vascular diseases, specifically coronary heart disease, serious cardiac arrhythmias, or vasospastic diseases. In these situations, the potential risks of using NICOTROL Inhaler should be discussed with the patient.

 

Please see full prescribing information.

NICOTROL® Inhaler (nicotine inhalation system)

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