This is normal.Gently hold pressure over your skin with a cotton ball or gauze until the bleeding stops.If needed, cover the injection site with a small bandage.Throw away the cap and other used supplies in your household trash.If you do not have a FDA-cleared sharps disposal container, you may use a household container that is:When your sharps disposal container is almost full, you will need to follow your community guidelines for the right way to dispose of your sharps disposal container. 2.3 . For the purposes of the OCS dose titration, asthma control was assessed by the investigator based on a patient’s FEVWhile 2 dosing regimens were studied in Trials 1, 2, and 3, the recommended dosing regimen is 30 mg Fasenra administered every 4 weeks for the first 3 doses, then every 8 weeks thereafter The primary endpoint for Trials 1 and 2 was the rate of asthma exacerbations in patients with baseline blood eosinophil counts of greater than or equal to 300 cells/μL who were taking high-dose ICS and LABA. In a prenatal and postnatal development study conducted in cynomolgus monkeys, there was no evidence of fetal harm with IV administration of benralizumab throughout pregnancy at doses that produced exposures up to approximately 310 times the exposure at the maximum recommended human dose (MRHD) of 30 mg SC [see In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively.In women with poorly or moderately controlled asthma, evidence demonstrates that there is an increased risk of preeclampsia in the mother and prematurity, low birth weight, and small for gestational age in the neonate. Always consult your healthcare provider to ensure …
Fasenra is indicated for the add-on maintenance treatment of patients with severe asthma aged 12 years and older, and with an eosinophilic phenotype [see Clinical Studies (14)].Limitations of use: FASENRA is intended for use under the guidance of a healthcare provider. A patient may self-inject or the patient caregiver may administer FASENRA PEN subcutaneously after the healthcare provider determines it is appropriate. A patient may self-inject or the patient caregiver may administer FASENRA PEN subcutaneously after the healthcare provider determines it is appropriate. Reductions of 50% or higher in the OCS dose were observed in 48 (66%) patients receiving Fasenra compared to those receiving placebo 28 (37%). Select one or more newsletters to continue. The recommended dose of FASENRA is 30 mg administered once every 4 weeks for the first 3 doses, and then once every 8 weeks thereafter by subcutaneous injection into the upper arm, thigh, or abdomen.Do not remove needle cover until ready to inject. FASENRA is clear to opalescent, colorless to slightly yellow, and may contain a few translucent or white to off-white particles. In the event of a hypersensitivity reaction, Fasenra should be discontinued Fasenra should not be used to treat acute asthma symptoms or acute exacerbations. These reactions generally occurred within hours of Fasenra administration, but in some instances had a delayed onset (i.e., days). Hold the syringe body and remove the needle cover by pulling straight off. Benralizumab crossed the placenta in cynomolgus monkeys. Do not give Fasenra to other people, even if they have the same symptoms you have. These reactions generally occur within hours of administration, but in some instances have a delayed onset (i.e., days).
Release pressure on the plunger head to allow the needle guard to cover the needle. Do not remove the cap until you have reached Step 6 of these instructions and are ready to inject Fasenra.. For these reasons, comparison of the incidence of antibodies to benralizumab in the studies described below with the incidence of antibodies in other studies or to other products may be misleading.Overall, treatment-emergent anti-drug antibody response developed in 13% of patients treated with Fasenra at the recommended dosing regimen during the 48 to 56 week treatment period.
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