Stelara

Generic Name/API: Ustekinumab
Manufacturer: Janssen Biotech, Inc.
Packaging: Single-dose Prefilled Syringe
Storage: 25°C
Dosage: 45 mg/90 mg; Intravenous
Strength: 136 mg, 90mg, 45mg single-dose vial
Indication: Ustekinumab or Stelara is a prescribed medicine primarily used to treat Psoriatic Arthritis, Plaque Psoriasis, Ulcerative colitis, or Crohn's disease. If Stelara is not approved in patient's home country, Sansfro can assist you in importing this product through the Named Patient Program.
No Indian generic option is available.
 
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About Ustekinumab or Stelara

Ustekinumab or Stelara, Interleukin (IL) 12 – IL 23 antagonist prescribed to treat patients with cases including:

  • Moderate to severe plaque psoriasis for candidates undergoing phototherapy.
  • Adults with active psoriatic arthritis, with or without the use of the drug methotrexate.
  • Individuals with moderately to severely active Crohn’s disease who have tried other medications without results.
  • Individuals with moderately to extremely active ulcerative colitis who have tried various medications without results.

Strength

  • 130 mg/26 mL (5 mg/mL) solution in a single-dose vial for intravenous infusion.
  • 45 mg/0.5 mL in a single-dose vial and  45 mg/0.5 mL or 90 mg/mL in a single-dose prefilled syringe for subcutaneous infusion. 

Recommended Dosage 

The dosage of Ustekinumab may vary based on the patient’s weight. 

Psoriasis Adult

  • In adult Psoriasis with weight under 100 kgs, initial subcutaneous administration of 45 mg, followed by subcutaneous administration of 45 mg every 4 weeks for the next 12 weeks.
  • In adult Psoriasis with weight greater than 100 kgs, Initial subcutaneous administration of 90 mg, followed by subcutaneous administration of 90 mg every 4 weeks for the next 12 weeks.

Psoriasis Adolescent

It is advised to administer medications for Psoriasis Adolescent (12 years and older) depending on weight at the first dose, 4 weeks later, and then every 12 weeks after that.

  • 0.75 mg/kg for weight less than 60 kgs, 45 mg for weight between 60-100 kgs, and 90 mg for greater than 100 kgs with subcutaneous administration. 

Adult Psoriatic Arthritis

  • The recommended dosage is 45 mg delivered subcutaneously initially, followed by 4 weeks later, and then every 12 weeks after that. 
  • The suggested dosage is 90 mg taken subcutaneously initially and 4 weeks later, followed by 90 mg administered subcutaneously every 12 weeks, for patients with co-existing moderate-to-severe plaque psoriasis who weigh more than 100 kg.

Crohn’s Disease

  • The recommended intravenous dosage recommendation for Crohn’s disease is 260 mg (2 vials) for patients with weight up to 55 kg
  • 390 mg (3 vials) for patients with weight between 55-85 kg
  • 520 mg (4 vials) for patients with weight greater than 85 kg. 

Important: In case of severe effects of the medication, kindly connect with your doctor. 


Warnings & Precautions

  • ustekinumab should not be used to treat any clinically significant active infection. Discontinue the use of ustekinumab if a major infection or clinically significant infection appears until the infection clears itself. 
  • Mycobacteria, salmonella, and Bacillus Calmette-Guerin (BCG) immunizations have all been linked to serious illnesses in people who are genetically weak in IL-12/IL-23. Consider diagnostic tests for these infections when warranted by the clinical situation. 
  • Check for TB in patients before starting ustekinumab medication. Start latent TB treatment before taking ustekinumab. 
  • There might be higher risks of cancer. It has not been determined whether ustekinumab is safe for use in patients with a history of or known cancer.
  • It’s possible to experience anaphylaxis or other clinically serious hypersensitivity events after taking ustekinumab. 
  • In the case of Leukoencephalopathy Syndrome, the patient must discontinue the use of ustekinumab and treat it immediately. 
  • During the post-approval usage of ustekinumab, cases of interstitial pneumonia, eosinophilic pneumonia, and cryptogenic organizing pneumonia have been recorded. Discontinue the use of ustekinumab if the diagnosis is confirmed, and start the recommended treatments.

Common ustekinumab Side Effects

  • Nasopharyngitis
  • Upper respiratory tract infection
  • Headache
  • Fatigue
  • Vomiting

Severe Reactions of ustekinumab

  • There might be a high risk of certain infections.
  • Patients may also experience decreased immune system activity and a high risk of certain cancer types. 

Storage & Handling 

The diluted infusion solution may be kept at room temperature up to 25°C (77°F) for up to 4 hours. Avoid freezing. Any unused infusion solution should be thrown away.

We follow a four-step process to procure the medicines:

  • Enquiry about the medicines: You submit a request for information about the medications you require using our portal, and we process your data. Within 24 hours, a member of our Named Access Program Support will get in touch with you and provide you with all the assistance you need.
  • Verification Process: As we assist patients in finding medications that are not yet approved and readily available in their home countries, Sansfro must confirm the availability and approval of the medicines they need. We also check the patient’s prescription and medical information.
  • Sourcing the Medicine: After the verification process has been successfully completed, our staff will contact our vast network of suppliers to find your medicine. Following the process, our team gets the best rates of the medicines for you and ensures processing.
  • Safe Delivery: We will set up the consignment’s safe delivery after the final quote is approved. Additionally, our logistics experts can help you track your consignment. The Named Access Program industry has a large number of unauthorized channels. To provide the medications safely and legally, we do so by adhering to the Standard Operating Procedures.

When importing medication, we will need the following documents from the patient:

  1. A valid prescription copy.
  2. An identity proof document.
  3. Details of the attending healthcare professional.
  4. A current address.

Once we have all these documents, the Sansfro team will initiate the application process for an import license. This license is essential to ensure that we can obtain the necessary medication once it receives government approval.

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About Sansfro

Sansfro is committed to bridging the healthcare gap. Our purpose is to bring hope and healing to patients suffering from rare diseases by linking them with life-saving treatments through our Named Patient Program. Join us in our quest for a better and healthier world.

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FAQ'S

How does ustekinumab or Stelara work?

Stelara functions by specifically fighting the immune system proteins that support the emergence of autoimmune disorders. ustekinumab aids in symptom management and inflammation reduction by obstructing these proteins.

Which particular medical conditions does Stelara treat?

The recommended dosage of ustekinumab treats Adults with moderate to severe plaque psoriasis and active psoriatic arthritis typically use Stelara.

What is the cost of a Stelara injection?

Stelara injection cost depends on the product requirement and the country where the product is ordered. Request more details by reaching out to our Patient Support Team at ‎(+91) 93157 05373 or help@invimeds.com

What are the potential side effects of Stelara?

Stelara side effects might include headache, fatigue, vomiting, injection site reactions, and gastrointestinal symptoms. Patients may experience high risks of certain infections including bacterial, viral, and fungus. 

Dr Anchal Aryan

Medical counselor

Patient Support Head Detail

Dr Anchal Aryan

Medical counselor

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