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Models for illustrative purposes only.
Select each patient to learn how to identify which types of patients in your practice may benefit
from PALFORZIA.
Aspiring adventurer
Hopeful student,
severely allergic
Budding athlete
Independence seeker
Shortly after snack time at a mother and baby group, Aaron consumed part of a muffin that contained peanuts that an older child had left on a nearby playmat. That led to his first allergic reaction and a visit to the emergency room. This was followed up at an allergy clinic where his peanut allergy was diagnosed.
Aaron started treatment with PALFORZIA early at the age of 1. Upon a recheck of IgE after a year of treatment, Aaron showed improved immunomodulation which helped protect him after he accidentally ate another child’s peanut butter cookie on the playground.
During a family outing to a restaurant, Oliver consumed a meal with trace amounts of peanuts, despite his mother thoroughly checking the menu and informing staff of his allergy. This resulted in a visit to the emergency room to treat his anaphylactic reaction.
PALFORZIA increased Oliver’s tolerability to peanuts after 2 years on treatment and thereby decreasing his sensitivity.
Now, knowing he is better protected against accidental exposure, Oliver and his mom are able to focus on the excitement of a new school and new friendships instead of his peanut allergy.
At a climbing competition away from home, Anna required epinephrine administration and a visit to the emergency room after she accidentally consumed a snack that unknowingly contained peanuts. The snack was given to her by a teammate, despite her team and coaches’ awareness of her allergy. This caused concerns from her parents about her safety out of their supervision.
Building Anna’s tolerability to peanut has allowed her the opportunity to pursue her passion for rock climbing without requiring the strict supervision by her parents.
While at a local festival, she was served fries cooked in peanut oil without proper allergy guidance, resulting in a significant reaction and the need for epinephrine to be administered.
Since Lucy feels she has more protection against accidental exposures, her future college plans and living away from home are less of a concern for both Lucy and her parents.
*The patients portrayed and their associated data are fictional, hypothetical, and they have not actually been treated with PALFORZIA. Individual results will vary with each patient.
Discover how through shared decision making with their
allergist, they chose PALFORZIA treatment.
†Individual results will vary with each patient.
These are real caregivers of real patients who are taking or have taken PALFORZIA and have been compensated for their time.
Healthcare professionals featured are real physicians who treat or have treated patients with PALFORZIA and have been compensated for their time.
The patient images are AI generated and are not real
patients treated with PALFORZIA. Individual results will
vary with each patient.
IgE, immunoglobulin E; REMS, Risk Evaluation and Mitigation Strategy.
References:
WARNING: ANAPHYLAXIS
INDICATION
PALFORZIA is an oral immunotherapy indicated for the mitigation of allergic reactions, including anaphylaxis, that may occur with accidental exposure to peanut.
PALFORZIA is approved for use in patients with a confirmed diagnosis of peanut allergy. Initial Dose Escalation may be administered to patients aged 1 through 17 years. Up-Dosing and Maintenance may be continued in patients 1 years of age and older.
PALFORZIA is to be used in conjunction with a peanut-avoidant diet.
Limitation of Use: Not indicated for the emergency treatment of allergic reactions, including anaphylaxis.
CONTRAINDICATIONS
PALFORZIA is contraindicated in patients with uncontrolled asthma, or with a history of eosinophilic esophagitis and other eosinophilic gastrointestinal disease.
WARNINGS AND PRECAUTIONS
ANAPHYLAXIS
PALFORZIA can cause anaphylaxis, which may be life-threatening. PALFORZIA is available only through a restricted program under a Risk Evaluation and Mitigation Strategy (REMS) called the PALFORZIA REMS because of the risk of anaphylaxis. Only prescribers, healthcare settings, pharmacies, and patients certified and enrolled in the REMS Program can prescribe, receive, dispense or administer PALFORZIA.
Anaphylaxis has been reported during all phases of PALFORZIA dosing, including Maintenance and in subjects who have undergone recommended Up-Dosing and dose modification procedures.
Do not initiate PALFORZIA treatment in a patient who has had severe or life-threatening anaphylaxis within the previous 60 days. PALFORZIA may not be suitable for patients with certain medical conditions that may reduce the ability to survive anaphylaxis, including but not limited to markedly compromised lung function, severe mast cell disorder, or cardiovascular disease. In addition, PALFORZIA may not be suitable for patients taking medications that can inhibit or potentiate the effects of epinephrine.
All Initial Dose Escalation doses and the first dose of each Up-Dosing level must be administered under observation in a certified health care setting.
Patients may be more likely to experience allergic reactions following PALFORZIA administration in the presence of cofactors such as exercise, hot water exposure, intercurrent illness (e.g., viral infection), or fasting. Other potential cofactors may include menstruation, sleep deprivation, nonsteroidal anti-inflammatory drug use, or uncontrolled asthma. Patients should be proactively counseled about the potential for the increased risk of anaphylaxis in the presence of these cofactors. If possible, adjust the time of dosing to avoid these cofactors. If it is not possible to avoid these cofactors, consider withholding PALFORZIA temporarily.
ASTHMA
Uncontrolled asthma is a risk factor for a serious outcome, including death, in anaphylaxis. Ensure patients with asthma have their asthma under control prior to initiation of PALFORZIA.
PALFORZIA should be temporarily withheld if the patient is experiencing an acute asthma exacerbation. Following resolution of the exacerbation, resumption of PALFORZIA should be undertaken cautiously. Re-evaluate patients who have recurrent asthma exacerbations and consider discontinuation of PALFORZIA.
EOSINOPHILIC GASTROINTESTINAL DISEASE
Discontinue PALFORZIA and consider a diagnosis of eosinophilic esophagitis in patients who experience severe or persistent gastrointestinal symptoms, including dysphagia, vomiting, nausea, gastroesophageal reflux, chest pain, or abdominal pain.
GASTROINTESTINAL ADVERSE REACTIONS
Gastrointestinal adverse reactions were commonly reported in PALFORZIA-treated subjects, and dose modification should be considered for patients who report these reactions. For severe or persistent gastrointestinal symptoms consider a diagnosis of eosinophilic esophagitis.
ADVERSE REACTIONS
The most common adverse reactions reported in subjects ages 1 through 3 years treated with PALFORZIA (incidence ≥5%) are cough, sneezing, rhinitis, nasal congestion, throat irritation, wheezing, abdominal pain, vomiting, diarrhea, oral pruritus, oropharyngeal pain, urticaria, rash, pruritus, and perioral dermatitis.
The most common adverse events reported in subjects ages 4 through 17 years treated with PALFORZIA (incidence ≥ 5% and at least 5% greater than placebo) are abdominal pain, vomiting, nausea, oral pruritus, oral paresthesia, throat irritation, cough, rhinorrhea, sneezing, throat tightness, wheezing, dyspnea, pruritus, urticaria, anaphylactic reaction, and ear pruritus.
Please see full Prescribing Information, including Boxed WARNING and Medication Guide.