Treatment support resources?YES

We’ve got services and tools to help you and your patients get the most out of  Yesintek™

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My Biocon Biologics™ provides access support for patients starting or switching to YESINTEK

Patient Transition Program*

Offers existing Stelara® (ustekinumab) or other ustekinumab biosimilar patients a prepaid $250 Health Debit Card to help make the switch to YESINTEK (ustekinumab-kfce) as seamless as possible

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IV Savings Program†

Gives eligible new patients savings up to $100 in out-of-pocket costs associated with the initial IV induction dose for gastrointestinal conditions

Transition Program Card 1
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Patient Transition Program*

Offers existing Stelara® (ustekinumab) or other ustekinumab biosimilar patients a prepaid $250 Health Debit Card to help make the switch to YESINTEK (ustekinumab-kfce) as seamless as possible

Transition Program Card 1

IV Savings Program†

Gives eligible new patients savings up to $100 in out-of-pocket costs associated with the initial IV induction dose for gastrointestinal conditions

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Benefits Investigation


Handles research of insurance coverage and patient cost-sharing, while providing a full summary of benefits

Quick Start Program‡

Provides a way for new patients to quickly begin therapy if the prior authorization or appeal process takes 5 days or longer

Prior Authorization Support
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Prior Authorization Support


Helps you with verifying the enrollment status of your patient’s insurance plan

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Bridge Program‡

Helps minimize authorization-related treatment delays for existing patients and deliver prescription to their door

*Eligibility restrictions apply. Available for patients transitioning from Stelara or other ustekinumab to YESINTEK. For full terms and conditions, visit  www.Yesintek.com/patienttransitionprogram.

†Eligibility restrictions apply. Not valid for uninsured patients or patients who are covered by a state- or federally funded healthcare program. For full terms and conditions,
visit www.Yesintek.com/IVsavingsprogram.

‡Eligibility restrictions apply. For the Quick Start and Bridge Program terms and conditions, visit www.YesintekHCP.com/bridgeprogramtermsandconditions.
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Benefits Investigation


Handles research of insurance coverage and patient cost-sharing, while providing a full summary of benefits

Prior Authorization Support


Helps you with verifying the enrollment status of your patient’s insurance plan

Quick Start Program‡

Provides a way for new patients to quickly begin therapy if the prior authorization or appeal process takes 5 days or longer

Bridge Program‡

Helps minimize authorization-related treatment delays for existing patients and deliver prescription to their door

*Eligibility restrictions apply. For the Quick Start and Bridge Program terms and conditions, please visit www.YesintekHCP.com/bridgeprogramtermsandconditions.

†Eligibility restrictions apply. Not valid for uninsured patients or patients who are covered by a state- or federally funded healthcare program. For full terms and conditions, visit www.Yesintek.com/IVsavingsprogram.

*Eligibility restrictions apply. Available for patients transitioning from Stelara or other ustekinumab 
to YESINTEK. For full terms and conditions, visit
www.Yesintek.com/patienttransitionprogram

†Eligibility restrictions apply. Not valid for uninsured patients or patients who are covered by a state- or federally funded healthcare program. For full terms and conditions, visit www.Yesintek.com/IVsavingsprogram.

‡Eligibility restrictions apply. For the Quick Start and Bridge Program terms and conditions, please visit www.YesintekHCP.com/bridgeprogramtermsandconditions.

Copay assistance§

We’ll help you identify and enroll your eligible patients who may pay as little as $0 in out-of-pocket costs.

§Eligibility restrictions apply. Not valid for uninsured patients or patients who are covered by a state- or federally funded healthcare program. For full terms and conditions, visit www.Yesintek.com/copay.

Yesintek copay card
ENROLL PATIENTS
For questions or help with patient enrollment, My Biocon Biologics patient access specialists are available Monday-Friday, 8 AM-8 PM ET at 1-833-61-BIOCON (or 1-833-612-4626).

For questions or help with patient enrollment, My Biocon Biologics patient access specialists are available Monday-Friday, 8 AM-8 PM ET at 1-833-61-BIOCON (or 1-833-612-4626).

ENROLL PATIENTS

Resources for your practice

Coding and Billing Guide

Provides you with information specific to the coding and administration of YESINTEK.

Click to download
Click to download

Enrollment Forms

Forms for getting your patients enrolled in the My Biocon Biologics support program.

Click to download
Click to download

Resources for your patient

Patient Brochure

A printable booklet with detailed product information to help your patient get familiar with YESINTEK.

Click to download
Click to download

Self-Injection Training

A step-by-step video tutorial on how to correctly use the YESINTEK prefilled syringe.

Click To Watch
CLICK TO WATCH

Restroom Access Overview

A resource outlining the law that gives your patient access to public restrooms when it’s most needed.

Click to download
Click to download

INDICATIONS AND IMPORTANT SAFETY INFORMATION

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IMPORTANT SAFETY INFORMATION

Contraindications
YESINTEK is contraindicated in patients with clinically significant hypersensitivity to ustekinumab or to any of the excipients.
Infections
YESINTEK may increase the risk of infections and reactivation of latent infections. Serious bacterial, mycobacterial, fungal, and viral infections in patients receiving ustekinumab.
Serious infections requiring hospitalization or otherwise clinically significant infections:

  • Plaque Psoriasis: diverticulitis, cellulitis, pneumonia, appendicitis, cholecystitis, sepsis, osteomyelitis, viral infections, gastroenteritis, and urinary tract infections.
  • Psoriatic arthritis: cholecystitis.
  • Crohn’s disease: anal abscess, gastroenteritis, ophthalmic herpes zoster, pneumonia, and Listeria meningitis.
  • Ulcerative colitis: gastroenteritis, ophthalmic herpes zoster, pneumonia, and listeriosis.

Treatment with YESINTEK should not be initiated in patients with a clinically important active infection until the infection resolves or is adequately treated. Consider the risks and benefits of treatment prior to initiating use of YESINTEK in patients with a chronic infection or a history of recurrent infection.
Instruct patients to seek medical advice if signs or symptoms suggestive of an infection occur while on treatment with YESINTEK and discontinue YESINTEK for serious or clinically significant infections until the infection resolves or is adequately treated.
Theoretical Risk for Vulnerability to Particular Infections Individuals genetically deficient in IL-12/IL-23 are particularly vulnerable to disseminated infections from mycobacteria, Salmonella, and Bacillus Calmette-Guerin (BCG) vaccinations. Serious infections and fatal outcomes have been reported in such patients.
It is not known whether patients with pharmacologic blockade of IL-12/IL-23 from treatment with ustekinumab may be susceptible to these types of infections. Consider diagnostic testing, e.g., tissue culture, stool culture, as dictated by clinical circumstances.
Pre-Treatment Evaluation of Tuberculosis (TB) Evaluate patients for TB prior to initiating treatment with YESINTEK.
Do not administer YESINTEK to patients with active tuberculosis infection. Initiate treatment of latent TB before administering YESINTEK. Closely monitor patients receiving YESINTEK for signs and symptoms of active TB during and after treatment.
Malignancies: YESINTEK is an immunosuppressant and may increase the risk of malignancy. Malignancies were reported among patients who received ustekinumab in clinical trials.
The safety of ustekinumab has not been evaluated in patients who have a history of malignancy or who have a known malignancy.
There have been reports of the rapid appearance of multiple cutaneous squamous cell carcinomas in patients receiving ustekinumab who had risk factors for developing non-melanoma skin cancer (NMSC).
All patients receiving YESINTEK, especially those >60 years of age, those with a history of PUVA or prolonged immunosuppressant treatment, should be monitored for the appearance of NMSC.
Hypersensitivity Reactions: Hypersensitivity reactions, including anaphylaxis and angioedema, have been reported with ustekinumab. If an anaphylactic or other clinically significant hypersensitivity reaction occurs, institute appropriate therapy and discontinue YESINTEK.
Posterior Reversible Encephalopathy Syndrome (PRES): Two cases of posterior reversible encephalopathy syndrome (PRES), also known as Reversible Posterior Leukoencephalopathy Syndrome (RPLS), were reported in clinical trials. Cases have also been reported in post-marketing experience in patients with psoriasis, psoriatic arthritis and Crohn’s disease. Clinical presentation included headaches, seizures, confusion, visual disturbances, and imaging changes consistent with PRES a few days to several months after ustekinumab initiation. A few cases reported latency of a year or longer. Patients recovered with supportive care following withdrawal of ustekinumab.
Monitor all patients treated with YESINTEK for signs and symptoms of PRES. If PRES is suspected, promptly administer appropriate treatment and discontinue YESINTEK.
Immunizations Prior to initiating therapy with YESINTEK, patients should receive all age-appropriate immunizations as recommended by current immunization guidelines. Patients being treated with YESINTEK should avoid receiving live vaccines. Avoid administering BCG vaccines during treatment with YESINTEK or for one year prior to initiating treatment or one year following discontinuation of treatment. Caution is advised when administering live vaccines to household contacts of patients receiving YESINTEK because of the potential risk for shedding from the household contact and transmission to patient.
Non-live vaccinations received during a course of YESINTEK may not elicit an immune response sufficient to prevent disease.
Noninfectious Pneumonia Cases of interstitial pneumonia, eosinophilic pneumonia, and cryptogenic organizing pneumonia have been reported during post-approval use of ustekinumab. Clinical presentations included cough, dyspnea, and interstitial infiltrates following one to three doses. Serious outcomes have included respiratory failure and prolonged hospitalization. Patients improved with discontinuation of therapy and, in certain cases, administration of corticosteroids. If diagnosis is confirmed, discontinue YESINTEK and institute appropriate treatment.
Allergen Immunotherapy YESINTEK may decrease the protective effect of allergen immunotherapy (decrease tolerance) which may increase the risk of an allergic reaction to a dose of allergen immunotherapy. Therefore, caution should be exercised in patients receiving or who have received allergen immunotherapy, particularly for anaphylaxis.
Most Common Adverse Reactions

  • Psoriasis: nasopharyngitis, upper respiratory tract infection, headache, and fatigue.
  • Crohn’s Disease, induction: vomiting.
  • Crohn’s Disease, maintenance: nasopharyngitis, injection site erythema, vulvovaginal candidiasis/mycotic infection, bronchitis, pruritus, urinary tract infection, and sinusitis.
  • Ulcerative colitis, induction: nasopharyngitis.
  • Ulcerative colitis, maintenance: nasopharyngitis, headache, abdominal pain, influenza, fever, diarrhea, sinusitis, fatigue, and nausea.

INDICATIONS

YESINTEK (ustekinumab-kfce) is a human interleukin-12 and -23 antagonist indicated for the treatment of: Adult patients with: moderate to severe plaque psoriasis (PsO) who are candidates for phototherapy or systemic therapy; active psoriatic arthritis (PsA); moderately to severely active Crohn’s disease (CD); moderately to severely active ulcerative colitis.
Pediatric patients 6 years and older with: moderate to severe plaque psoriasis, who are candidates for phototherapy or systemic therapy; active psoriatic arthritis (PsA).

INDICATIONS AND IMPORTANT SAFETY INFORMATION

IMPORTANT SAFETY INFORMATION

Contraindications
YESINTEK is contraindicated in patients with clinically significant hypersensitivity to ustekinumab or to any of the excipients.
Infections
YESINTEK may increase the risk of infections and reactivation of latent infections. Serious bacterial, mycobacterial, fungal, and viral infections in patients receiving ustekinumab.
Serious infections requiring hospitalization or otherwise clinically significant infections:

  • Plaque Psoriasis: diverticulitis, cellulitis, pneumonia, appendicitis, cholecystitis, sepsis, osteomyelitis, viral infections, gastroenteritis, and urinary tract infections.
  • Psoriatic arthritis: cholecystitis.
  • Crohn’s disease: anal abscess, gastroenteritis, ophthalmic herpes zoster, pneumonia, and Listeria meningitis.
  • Ulcerative colitis: gastroenteritis, ophthalmic herpes zoster, pneumonia, and listeriosis.

Treatment with YESINTEK should not be initiated in patients with a clinically important active infection until the infection resolves or is adequately treated. Consider the risks and benefits of treatment prior to initiating use of YESINTEK in patients with a chronic infection or a history of recurrent infection.
Instruct patients to seek medical advice if signs or symptoms suggestive of an infection occur while on treatment with YESINTEK and discontinue YESINTEK for serious or clinically significant infections until the infection resolves or is adequately treated.
Theoretical Risk for Vulnerability to Particular Infections Individuals genetically deficient in IL-12/IL-23 are particularly vulnerable to disseminated infections from mycobacteria, Salmonella, and Bacillus Calmette-Guerin (BCG) vaccinations. Serious infections and fatal outcomes have been reported in such patients.
It is not known whether patients with pharmacologic blockade of IL-12/IL-23 from treatment with ustekinumab may be susceptible to these types of infections. Consider diagnostic testing, e.g., tissue culture, stool culture, as dictated by clinical circumstances.
Pre-Treatment Evaluation of Tuberculosis (TB) Evaluate patients for TB prior to initiating treatment with YESINTEK.
Do not administer YESINTEK to patients with active tuberculosis infection. Initiate treatment of latent TB before administering YESINTEK. Closely monitor patients receiving YESINTEK for signs and symptoms of active TB during and after treatment.
Malignancies: YESINTEK is an immunosuppressant and may increase the risk of malignancy. Malignancies were reported among patients who received ustekinumab in clinical trials.
The safety of ustekinumab has not been evaluated in patients who have a history of malignancy or who have a known malignancy.
There have been reports of the rapid appearance of multiple cutaneous squamous cell carcinomas in patients receiving ustekinumab who had risk factors for developing non-melanoma skin cancer (NMSC).
All patients receiving YESINTEK, especially those >60 years of age, those with a history of PUVA or prolonged immunosuppressant treatment, should be monitored for the appearance of NMSC.
Hypersensitivity Reactions: Hypersensitivity reactions, including anaphylaxis and angioedema, have been reported with ustekinumab. If an anaphylactic or other clinically significant hypersensitivity reaction occurs, institute appropriate therapy and discontinue YESINTEK.
Posterior Reversible Encephalopathy Syndrome (PRES): Two cases of posterior reversible encephalopathy syndrome (PRES), also known as Reversible Posterior Leukoencephalopathy Syndrome (RPLS), were reported in clinical trials. Cases have also been reported in post-marketing experience in patients with psoriasis, psoriatic arthritis and Crohn’s disease. Clinical presentation included headaches, seizures, confusion, visual disturbances, and imaging changes consistent with PRES a few days to several months after ustekinumab initiation. A few cases reported latency of a year or longer. Patients recovered with supportive care following withdrawal of ustekinumab.
Monitor all patients treated with YESINTEK for signs and symptoms of PRES. If PRES is suspected, promptly administer appropriate treatment and discontinue YESINTEK.
Immunizations Prior to initiating therapy with YESINTEK, patients should receive all age-appropriate immunizations as recommended by current immunization guidelines. Patients being treated with YESINTEK should avoid receiving live vaccines. Avoid administering BCG vaccines during treatment with YESINTEK or for one year prior to initiating treatment or one year following discontinuation of treatment. Caution is advised when administering live vaccines to household contacts of patients receiving YESINTEK because of the potential risk for shedding from the household contact and transmission to patient.
Non-live vaccinations received during a course of YESINTEK may not elicit an immune response sufficient to prevent disease.
Noninfectious Pneumonia Cases of interstitial pneumonia, eosinophilic pneumonia, and cryptogenic organizing pneumonia have been reported during post-approval use of ustekinumab. Clinical presentations included cough, dyspnea, and interstitial infiltrates following one to three doses. Serious outcomes have included respiratory failure and prolonged hospitalization. Patients improved with discontinuation of therapy and, in certain cases, administration of corticosteroids. If diagnosis is confirmed, discontinue YESINTEK and institute appropriate treatment.
Allergen Immunotherapy YESINTEK may decrease the protective effect of allergen immunotherapy (decrease tolerance) which may increase the risk of an allergic reaction to a dose of allergen immunotherapy. Therefore, caution should be exercised in patients receiving or who have received allergen immunotherapy, particularly for anaphylaxis.
Most Common Adverse Reactions

  • Psoriasis: nasopharyngitis, upper respiratory tract infection, headache, and fatigue.
  • Crohn’s Disease, induction: vomiting.
  • Crohn’s Disease, maintenance: nasopharyngitis, injection site erythema, vulvovaginal candidiasis/mycotic infection, bronchitis, pruritus, urinary tract infection, and sinusitis.
  • Ulcerative colitis, induction: nasopharyngitis.
  • Ulcerative colitis, maintenance: nasopharyngitis, headache, abdominal pain, influenza, fever, diarrhea, sinusitis, fatigue, and nausea.

INDICATIONS

YESINTEK (ustekinumab-kfce) is a human interleukin-12 and -23 antagonist indicated for the treatment of: Adult patients with: moderate to severe plaque psoriasis (PsO) who are candidates for phototherapy or systemic therapy; active psoriatic arthritis (PsA); moderately to severely active Crohn’s disease (CD); moderately to severely active ulcerative colitis.
Pediatric patients 6 years and older with: moderate to severe plaque psoriasis, who are candidates for phototherapy or systemic therapy; active psoriatic arthritis (PsA).

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Enroll Your Patient Today

Download the <Yesintek Copay Assistance Program> Enrollment and Prescription Form

Download the
<Yesintek Copay Assistance Program> Enrollment and Prescription Form

Then fax your completed form to 1-<XXX-XXX-XXXX>.

Download the Form

You can also e-prescribe your YESINTEK prescription by searching for <NAME TBD> in your EHR.* Be sure to include your patient’s mobile number.†

*<ADDRESS TBD>

†By providing the patient’s phone number, you represent that your patient is aware of the disclosure and has given consent to be contacted 
 regarding this prescription, and by the fulfillment pharmacy.

EHR=electronic health record.

INDICATIONS

YESINTEK (ustekinumab-kfce) is a human interleukin-12 and -23 antagonist indicated for the treatment of:

  • Adult patients with:
  • moderate to severe plaque psoriasis (PsO) who are candidates for phototherapy or systemic therapy
  • active psoriatic arthritis (PsA)
  • moderately to severely active Crohn’s disease (CD)
  • moderately to severely active ulcerative colitis
  • Pediatric patients 6 years and older with:
  • moderate to severe plaque psoriasis, who are candidates for phototherapy or systemic therapy
  • active psoriatic arthritis (PsA)