Rheumatology Enrollment Form Fax Referral To: Phone: Fax Referral To: 800-323-2445 Email Referral To: Email Referral To: [email protected] Phone: 800-237-2767 6 Simple steps to submitting a referral u PATIENT INFORMATION v PRESCRIPTION INFORMATION (Complete the following or include demographic sheet) Patient Name: Address: City, State, Zip: Primary Phone: Home Cell Work Alternate Phone: Home Cell Work DOB: Gender: Male Female E-mail: Last Four of SS #: Primary Language: Prescriber’s Name: State License #: DEA #: Group or Hospital: Address: City, State, Zip: Phone: Contact Person: w INSURANCE INFORMATION NPI # Fax: Phone: Please fax copy of prescription and insurance cards with this form, if available (front and back) x DIAGNOSIS AND CLINICAL INFORMATION Diagnosis (ICD-9 or ICD-10) 714.0 Rheumatoid Arthritis 720.0 Ankylosing Spondylitis Other: ____________________________________________________ Height:___________________ in/cm 696.0 Psoriatic Arthritis 714.3 Juvenile Idiopathic Arthritis ICD-10 Code & Description: ______________________________________ Weight: ___________________ kg/lbs Allergies:______________________________________________________ y PRESCRIPTION INFORMATION MEDICATION Actemra® DOSE/STRENGTH 80 mg/4 mL 200 mg/10 mL 400 mg/20 mL ___mg/kg DIRECTIONS Patients less than 100 kg weight 162 mg administered subcutaneously every other week, followed by an increase to every week based on clinical response Patients at or above 100 kg weight 162 mg administered subcutaneously every week Cimzia Starter Kit Induction dose: inject 400mg subcutaneously on day 1, at week 2, and at week 4 200mg/1 mL Prefilled Syringe 200mg vial Maint. Dose: Inject 200mg subcutaneously every OTHER week. Maint. Dose: Inject 400mg subcutaneously every 4 weeks. Other: _______________________________________________________________________ Enbrel®* 50mg/ml Sureclick™ Autoinjector 50mg/ml Prefilled Syringe 25mg/0.5ml Prefilled Syringe 25mg Vial Inject 50mg subcutaneously ONCE a week. Inject 25mg subcutaneously TWICE a week (72-96 hours apart). Other:________________________________________________________________________ Humira®* 40mg/0.8ml Pen 40mg/0.8ml Prefilled Syringe 20mg/0.4ml Prefilled Syringe Inject 40mg subcutaneously every OTHER week. Inject 20mg subcutaneously every OTHER week. Other:________________________________________________________________________ ILARIS® 4mg/kg (with a maximum of 300 mg) for patients with a body weight greater than or equal to 7.5kg. Administer subcutaneously every 4 weeks. ILARIS is supplied as a 180 mg white lyophilized powder for solution for subcutaneous injection. Reconstitution with 1 mL of preservative-free Sterile Water for injection is required prior to subcutaneous administration of the drug, resulting in a total volume of 1.2 mL reconstituted solution. Kineret® 100mg Prefilled Syringe Otezla® 1 kit (6 vials) 0 1 0 Inject 100mg (one syringe) SC once a day. 250mg Vial Infuse ______mg in 100ml of 0.9% NaCl at weeks 0, 2, and 4, then every 4 weeks thereafter. Other:________________________________________________________________________ 125mg Orencia Subcutaneous After single IV loading dose, inject 125mg subcutaneously within a day followed by 125mg subcutaneous injections every week thereafter. For patients unable to receive an IV loading dose, inject 125mg subcutaneously every week. For patients transitioning from IV infusion therapy to subcutaneous therapy, inject 125mg subcutaneously instead of the next scheduled IV dose followed by 125mg subcutaneous injections every week thereafter. Inject 125mg subcutaneously every week Titration Starter Pack Rx Take as Directed x14 days #27 tablets, 0 refills Orencia® REFILLS Induction dose: 4 mg/kg every 4 weeks Maint. Dose: (based on clinical response): 8mg/kg every 4 weeks Other:________________________________________________________________________ 162mg/0.9 mL Prefilled Syringe Cimzia® QUANTITY Maintenance dose 30mg tablet orally twice daily 30 MG Tablet Other:________________________________________________________________________ 100mg Vial Remicade® _______ mg/kg Induction Dose: IV in 250ml of 0.9% NaCl at weeks 0,2,and 6. (ICD-9: 714.0, 696.0, & 720.0) Maint. Dose: IV in 250ml of 0.9% NaCl every 8 weeks. (ICD-9: 714.0 & 696.0) Maint. Dose: IV in 250ml of 0.9% NaCl every 6 weeks. (ICD-9: 720.0) Other:________________________________________________________________________ Page 1 of 2 IMPORTANT NOTICE: Thistransmission facsimile transmission is intended to be delivered only toaddressee the named addressee andmaterial may contain that isprivileged, confidential, privileged, proprietary exempt from law.by If anyone it is IMPORTANT NOTICE: This facsimile is intended to be delivered only to the named and may contain that ismaterial confidential, proprietary or exampt from or disclosure underdisclosure applicableunder law. Ifapplicable it is received other than the named addressee,received the recipient shouldother immediately theaddressee, sender at the and telephone number notify set forth and instructions as to disposal of the In no even should material or retained by anyone than the named by anyone than thenotify named theaddress recipient should immediately theherein sender at obtain the address and telephone number settransmitted forth hereinmaterial. and obtain instructions as such to disposal of be theread transmitted material. In noother event addressee,should exceptsuch by express authority senderby to anyone the named addressee. RA 022614 material be readoforthe retained other than the named addressee, except by express authority of the sender to the named addressee. Hepatitis C 022514 Rheumatology Enrollment Form Fax Referral To: Fax Referral To: 800-323-2445 Email Referral To: Phone: Email Referral To: [email protected] Patient Information Phone: 800-237-2767 Patient Name:________________________________ DOB:______________ Prescriber’s Name:______________________ MEDICATION DOSE/STRENGTH DIRECTIONS QUANTITY Rituxan® 100mg/10ml vial 500mg/50ml vial Infuse two doses of 1000mg in 1 liter of 0.9% NaCl separated by 2 weeks. Other:________________________________________________________________________ Simponi® 50mg/0.5ml Prefilled SmartJect Autoinjector 50mg/0.5ml Prefilled Syringe Inject 50mg (0.5ml) subcutaneously once a month Other:________________________________________________________________________ Simponi® ARIA™ 50mg/4mL (12.5mg/ml) in a single use vial 2 mg/kg intravenous infusion over 30 minutes at weeks 0 and 4, then every 8 weeks Dilution of supplied SIMPONI ARIA solution with 0.9% w/v sodium chloride is required prior to administration. Stelara® Injection 45 mg/0.5 mL in a single-use prefilled syringe Injection: 90 mg/mL in a singleuse prefilled syringe The recommended dose is 45 mg SQ initially and 4 weeks later, followed by 45 mg SQ every 12 weeks. For patients with co-existent moderate-to-severe plaque psoriasis weighing>100kg (220 lbs), the recommended dose is 90 mg initially and 4 weeks later, followed by 90 mg every 12 weeks. Xelijanz® 5mg Take one 5mg tablet PO twice daily Other:________________________________________________________________________ Patient is interested in patient support programs STAMP SIGNATURE NOT ALLOWED z x__________________________________ DISPENSE AS WRITTEN REFILLS 60 120 180 Ancillary supplies and kits provided as needed for administration x__________________________________ (Date) PRODUCT SUBSTITUTION PERMITTED (Date) Page 2 of 2 IMPORTANT NOTICE: Thistransmission facsimile transmission to be delivered only toaddressee the named addressee and material may contain that isprivileged, confidential, privileged, proprietary exempt from applicable law.by If it is IMPORTANT NOTICE: This facsimile is intended is to intended be delivered only to the named and may contain that ismaterial confidential, proprietary or exampt fromor disclosure underdisclosure applicableunder law. If it is received anyone other than the named addressee,received the recipient shouldother immediately theaddressee, sender at the and telephone number notify set forth obtain instructions as to disposal of the In no even should material or retained by anyone by anyone than thenotify named theaddress recipient should immediately theherein senderand at the address and telephone number settransmitted forth hereinmaterial. and obtain instructions as such to disposal of be theread transmitted material. In noother eventthan the named addressee,should exceptsuch by express authority senderby toanyone the named addressee. RA 022614 material be readoforthe retained other than the named addressee, except by express authority of the sender to the named addressee. Hepatitis C 022514
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