Stay in the know with neffy
Enroll now to get news and updates and learn about programs and resources available to you and your patients.
do not fill or refill their prescription4*
do not consistently carry epinephrine5-7†
either delay or do not administer epinephrine at all during a type I allergic reaction8
*Based on 2023 IQVIA claims data.4
†Based on two surveys (917 adults and parents of children and adolescents who had been prescribed an epinephrine auto-injector and 35 pediatric patients with a documented history of food allergy) and an analysis of 587 food allergic reactions resulting from ingestion.5-7
ER, emergency room.
76% of patients said they would be more likely to carry a needle-free option10
Almost half of patients currently not filling their epinephrine needle-injector prescription would be more likely to fill a prescription for a needle-free option11‡
Patients and caregivers said they’d use a needle-free device earlier, reducing the time to dosing by 45%10§
Needle-free epinephrine may help eliminate the anxiety of using a needle-injector during the onset of an allergic reaction, that could lead to better patient outcomes.1,9,10
‡Based on a survey of 100 patients who had been diagnosed with severe or potentially life-threatening allergies.11
§Based on a 20-minute, double blind, web-based survey which included 100 caregivers and 100 qualifying patients who used an epinephrine injectable device within the 12 months prior to participating in the survey.10
Enroll now to get news and updates and learn about programs and resources available to you and your patients.
It is recommended that patients are prescribed and have immediate access to two neffy nasal sprays at all times. In the absence of clinical improvement or if symptoms worsen after initial treatment, administer a second dose of neffy in the same nostril with a new nasal spray starting 5 minutes after the first dose.
neffy is indicated for emergency treatment of type I allergic reactions, including anaphylaxis, in adult and pediatric patients aged 4 years and older who weigh 15 kg or greater.
neffy is for use in the nose only.
Advise patients when to seek emergency medical assistance for close monitoring of the anaphylactic episode and in the event further treatment is required.
Absorption of neffy may be affected by underlying structural or anatomical nasal conditions.
Administer with caution to patients who have heart disease; epinephrine may aggravate angina pectoris or produce ventricular arrhythmias. Arrhythmias, including fatal ventricular fibrillation, have been reported, particularly in patients with underlying cardiac disease or taking cardiac glycosides, diuretics, or anti-arrhythmics.
The presence of a sulfite in neffy should not deter use.
neffy may alter nasal mucosa for up to 2 weeks after administration and increase systemic absorption of nasal products, including neffy.
Patients with certain medical conditions or who take certain medications for allergies, depression, thyroid disorders, diabetes, and hypertension, may be at greater risk for adverse reactions.
Epinephrine can temporarily exacerbate the underlying condition or increase symptoms in patients with the following: hyperthyroidism, Parkinson’s disease, diabetes, renal impairment. Epinephrine should be administered with caution in patients with these conditions, including elderly patients and pregnant women.
Most common adverse reactions are nasal discomfort, headache, rhinorrhea, dizziness, nausea, vomiting, throat irritation, nasal congestion, paresthesia, sneezing, upper respiratory tract congestion, epistaxis, rhinalgia, nasal dryness, dry throat, fatigue, and feeling jittery.
These are not all of the possible side effects of neffy. To report suspected adverse reactions, contact ARS Pharmaceuticals Operations, Inc. at
Please see full Prescribing Information for neffy.