seller Sebelipase Alfa Overview Side Effects Dosage Professional Pregnancy More User Reviews Support Group Q & A Pronunciation (se be LYE pase AL fa) Index Terms SBC-102 Dosage Forms Excipient information presented when available (limited, particularly for generics); consult specific product labeling. Solution, Intravenous [preservative free]: Kanuma: 20 mg/10 mL (10 mL) [contains albumin human, egg white (egg protein)] Slideshow ADHD and Your Child: Signs and Treatment Options Brand Names: U.S. Kanuma Pharmacologic Category Enzyme, Replacement Therapy Pharmacology Sebelipase alfa binds to cell surface receptors via glycans expressed on the protein and is subsequently internalized into lysosomes. Sebelipase alfa catalyzes the lysosomal hydrolysis of cholesteryl esters and triglycerides to free cholesterol, glycerol, and free fatty acids. In patients with lysosomal acid lipase (LAL) deficiency, replacement with sebelipase alfa, a recombinant form of LAL, results in improvement in disease-related hepatic and lipid parameters. Distribution Pediatric patients: V d : 4 to 11 years: 3.6 3 L 12 to 17 years: 5.4 2.4 L Adults: V d : 5.3 1.6 L Onset of Action LDL-c and triglycerides reduction: Within 8 weeks; a transient increase in these values occurs during first 2 to 4 weeks of treatment. ALT reduction: Within 2 weeks. Time to Peak Serum: Children 4 years, Adolescents, and Adults: Mean range: 1.1 to 1.3 hours Duration of Action Effects on ALT partially reverse 3 weeks after treatment discontinuation (Balwani 2013). Half-Life Elimination Children 4 years, Adolescents, and Adults: Mean range: 5.4 to 6.6 minutes Use: Labeled Indications Lysosomal acid lipase deficiency: Treatment of patients with lysosomal acid lipase (LAL) deficiency Contraindications There are no contraindications listed within the manufacturer's labeling. Dosing: Adult Lysosomal acid lipase (LAL) deficiency: IV: 1 mg/kg every other week Dosing: Geriatric LAL deficiency: Refer to adult dosing; has not been studied. Dosing: Pediatric Rapidly progressive lysosomal acid lipase (LAL) deficiency presenting within the first 6 months of life: Infants: IV: Initial: 1 mg/kg once weekly; if response not optimal, may increase to 3 mg/kg once weekly LAL deficiency: Infants, Children, and Adolescents: IV: Refer to adult dosing. Dosing: Renal Impairment There are no dosage adjustments provided in the manufacturer s labeling. Dosing: Hepatic Impairment There are no dosage adjustments provided in the manufacturer s labeling. Dosing: Adjustment for Toxicity Mild or moderate hypersensitivity reaction: Interrupt infusion; consider resuming at slower infusion rate. Severe hypersensitivity reaction or anaphylaxis: Immediately discontinue infusion. Reconstitution Determine number of vials necessary for dose. After allowing vial(s) to reach room temperature, further dilute calculated dose volume with NS up to the manufacturer-recommended total infusion volume based on patient weight (refer to manufacturer s product labeling) to a final concentration range of 0.1 to 1.5 mg/mL. Mix gently by inversion. Do not shake vials or prepared infusion. Reconstituted solution should be clear to slightly opalescent, colorless to slightly colored solution. Thin, translucent particles or fibers may be present in vials or diluted solution. Vials are for single use only. Administration IV: Administer diluted solution as an IV infusion using low protein-binding infusion set with in-line, low protein-binding 0.2 micron filter. Infuse over at least 2 hours; may consider 1-hour infusion for those patients receiving 1 mg/kg dose who tolerate a 2-hour infusion. Consider further prolonging infusion time for 3 mg/kg dose or if hypersensitivity reaction occurs. Storage Store intact vials under refrigeration between 2 C to 8 C (36 F to 46 F) in original carton to protect from light. Do not shake or freeze. If not used immediately, reconstituted product may be stored up to 24 hours in the refrigerator. Drug Interactions There are no known significant interactions. Adverse Reactions Frequency not always defined. Incidences are reported for children, adolescents, and adult patients unless specified otherwise. Cardiovascular: Chest discomfort, oxygen saturation decreased (infants), tachycardia (infants) Central nervous system: Headache (28%), anxiety, hypotonia (infants) Dermatologic: Urticaria (infants: 33%) Endocrine & metabolic: Increase in LDL cholesterol (81%; mean increase of 18% at 2 and 4 weeks postinitiation), increased serum triglycerides (58%; mild increases that are transient) Gastrointestinal: Diarrhea (infants: 67%), vomiting (infants: 67%), constipation (8%), nausea (8%), retching (infants) Hematologic & oncologic: Anemia (infants: 44%) Hypersensitivity: Hypersensitivity reaction (20%; infants: 64%; children, adolescents, and adults: 13%), anaphylaxis (3%; may be delayed as late as 1 year after treatment initiation) Immunologic: Immunogenicity (infants: 57%; neutralizing and may affect drug efficacy: 29%; children, adolescents, and adults: 14%; neutralizing without any association on drug efficacy: 6%) Neuromuscular & skeletal: Weakness (8%) Respiratory: Rhinitis (infants: 56%), cough (infants: 33%), nasopharyngitis (infants: 33%; children and adult patients: 11%), oropharyngeal pain (17%), sneezing (infants) Miscellaneous: Fever (infants: 56%; children and adult patients: 25%) Warnings/Precautions Concerns related to adverse effects: Anaphylaxis/hypersensitivity reactions: Hypersensitivity reactions have occurred during infusion and within 4 hours after the infusion. Anaphylaxis has occurred as early as the sixth infusion and as late as 1 year after treatment initiation. During infusion, appropriate medical treatment should be immediately available. Depending on severity of hypersensitivity reaction, management may include temporary interruption, lowering infusion rate, and/or administration of antihistamines, antipyretics, and/or corticosteroids. If interrupted, the infusion may be resumed at a slower rate with increases as tolerated. Pretreatment with antipyretics and/or antihistamines may prevent subsequent reactions in those cases where symptomatic treatment was required. If anaphylaxis or severe hypersensitivity occurs, immediately discontinue infusion and initiate appropriate medical treatment. Antibody formation: Patients have developed anti-drug antibodies (ADA) to sebelipase alfa and may be more likely to experience hypersensitivity reactions. Some patients with neutralizing antibodies experienced decreased growth velocity. No clear association exists between the development of ADA and decreased efficacy in patients. Dosage form specific issues: Allergy to egg or egg products: Sebelipase alfa is produced in egg whites of genetically engineered chickens; consider the risks and benefits in patients with known systemic hypersensitivity reactions to eggs or egg products. Monitoring Parameters Signs and symptoms of hypersensitivity reaction (during infusion and for at least 4 hours after completion of infusion); lipid panel; anti-drug antibody assessment; hepatic function (ALT). Pregnancy Considerations Adverse events were not observed in animal reproduction studies. Sebelipase alfa is a recombinant form of lysosomal acid lipase (LAL), an essential enzyme required for lipid metabolism (Burton 2015; Shirley 2015). Patient Education Discuss specific use of drug and side effects with patient as it relates to treatment. (HCAHPS: During this hospital stay, were you given any medicine that you had not taken before? Before giving you any new medicine, how often did hospital staff tell you what the medicine was for? How often did hospital staff describe possible side effects in a way you could understand?) Patient may experience cough, nasal irritation, throat irritation, or constipation. Have patient report immediately to prescriber angina, tachycardia, shortness of breath, eyelid edema, rhinorrhea, fast breathing, abdominal pain, agitation, chills, severe diarrhea, edema, severe headache, severe dizziness, passing out, irritability, severe nausea, severe vomiting, pale skin, or severe loss of strength and energy (HCAHPS). Educate patient about signs of a significant reaction (eg, wheezing; chest tightness; fever; itching; bad cough; blue skin color; seizures; or swelling of face, lips, tongue, or throat). Note: This is not a comprehensive list of all side effects. Patient should consult prescriber for additional questions. Intended Use and Disclaimer: Should not be printed and given to patients. This information is intended to serve as a concise initial reference for health care professionals to use when discussing medications with a patient. You must ultimately rely on your own discretion, experience, and judgment in diagnosing, treating, and advising patients. Next Pregnancy Warnings Print this page Add to My Med List More about sebelipase alfa Side Effects During Pregnancy Dosage Information Support Group En Español 0 Reviews Add your own review/rating Drug class: lysosomal enzymes Consumer resources Sebelipase alfa Sebelipase alfa Intravenous (Advanced Reading) Professional resources Sebelipase Alfa (AHFS Monograph) Other brands: Kanuma Related treatment guides Lysosomal Acid Lipase Deficiency} Drug Status Rx Availability Prescription only N/A CSA Schedule Not a controlled drug Approval History Drug history at FDA Sebelipase alfa Rating No Reviews - Be the first! No Reviews - Be the first! Not Rated - Be the first! Drug Class Lysosomal enzymes Related Drugs lysosomal enzymes Fabrazyme , Lumizyme , Aldurazyme , Myozyme , Elaprase , cerliponase alfa Lysosomal Acid Lipase Deficiency Kanuma , More...} } it is also
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