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rilonacept
Arcalyst Pharmaceutical company:
Regeneron
www.regeneron.com

Pharmacologic classification: interleukin-1 blocker
Therapeutic classification:
immunosuppressant
Pregnancy risk category:
C


AVAILABLE FORMS
Single-use vial: 220 mg

INDICATIONS AND DOSAGES
Cryopyrin-associated periodic syndromes (CAPS), including familial cold autoinflammatory syndrome (FCAS) and Muckle-Wells syndrome (MWS)--
Adults: Loading dose of 320 mg, administered as two 160-mg (2-ml) subcutaneous injections given at different sites; then 160 mg (2 ml) subcutaneous injections once weekly.
Children age 12 to 17: Loading dose of 4.4 mg/kg up to a maximum of 320 mg subcutaneously, given at divided sites if necessary; then once weekly injections of 2.2 mg/kg up to a maximum 160 mg.

CONTRAINDICATIONS AND CAUTIONS
Contraindicated in those hypersensitive to drug.
   Use caution in presence of infection and in pregnant or breast-feeding patients.

INTERACTIONS
Drug-drug. Other interleukin blockers (anakinra) or tumor necrosis factor blockers (etanercept, adalimumab, infliximab) or corticosteroids: May increase the risk of serious infection. Avoid using together.

ADVERSE REACTIONS
CNS: hypoesthesia.
GI: nausea, diarrhea, stomach discomfort.
GU: UTI.
Hematologic: hyperlipidemia.
Respiratory: upper respiratory infection, sinusitis, cough.
Other: injection site reactions, immunosuppression.

Reactions may be common, uncommon, life-threatening, or
COMMON AND LIFE-THREATENING.

     
   

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