This information is for educational purposes only. It is not intended as medical advice. Always consult a qualified healthcare professional.
YESINTEK — Description, Dosage, Side Effects | PillsCard
Rx
YESINTEK
90 mg, Roztwór do wstrzykiwań w ampułko-strzykawce
INN: Ustekinumabum
Data updated: 2026-04-24
Available in:
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Form
Roztwór do wstrzykiwań w ampułko-strzykawce
Dosage
90 mg
Route
podskórna
Storage
Storage If necessary, the diluted infusion solution may be kept at room temperature up to 25°C (77°F) for up to 4 hours. Storage time at room temperature begins once the diluted solution has been prepared. The infusion should be completed within 4 hours after the dilution in the infusion bag (cumulative time after preparation including the storage and the infusion period). Do not freeze. Discard any unused portion of the infusion solution.
Storage and Stability Store YESINTEK vials and prefilled syringes refrigerated between 2°C to 8°C (36°F to 46°F). Store YESINTEK vials upright. Keep the product in the original carton to protect from light until the time of use. Do not freeze. Do not shake. If needed, individual prefilled syringes may be stored at room temperature up to 30°C (86°F) for a maximum single period of up to 30 days in the original carton to protect from light. Record the date when the prefilled syringe is first removed from the refrigerator on the carton in the space provided. Once a syringe has been stored at room temperature, do not return to the refrigerator. Discard the syringe if not used within 30 days at room temperature storage. Do not use YESINTEK after the expiration date on the carton or on the prefilled syringe.
Reviews reflect personal experiences and are not medical advice. Always consult your doctor.
About This Product
Manufacturer
Fresenius Kabi Deutschland GmbH (Austria)
Composition
Ustekinumabum 90 mg
ATC Code
L04AC05
Source
URPL
11 DESCRIPTION Ustekinumab-kfce, a human IgG1κ monoclonal antibody, is a human interleukin-12 and -23 antagonist. Using DNA recombinant technology, ustekinumab-kfce is produced in a murine cell line (Sp2/0). The manufacturing process contains steps for the clearance of viruses. Ustekinumab is comprised of 1326 amino acids and has an estimated molecular mass that ranges from 148,079 to 149,690 Daltons. YESINTEK (ustekinumab-kfce) injection is a sterile, preservative-free, clear and colorless to pale yellow solution with pH of 5.7- 6.3. YESINTEK for Subcutaneous Use Available as 45 mg of ustekinumab-kfce in 0.5 mL and 90 mg of ustekinumab-kfce in 1 mL, supplied as a sterile solution in a single-dose prefilled syringe with a 29 gauge fixed ½ inch needle and as 45 mg of ustekinumab-kfce in 0.5 mL in a single-dose Type I glass vial with a coated stopper. The syringe is fitted with a passive needle guard and a needle cover. Each 0.5 mL prefilled syringe or vial delivers 45 mg ustekinumab-kfce, histidine, L-histidine monohydrochloride monohydrate (0.5 mg), Polysorbate 80 (0.02 mg), and sucrose (38 mg). Hydrochloric acid and sodium hydroxide are used to adjust pH to 5.7- 6.3 during manufacturing. Each 1 mL prefilled syringe delivers 90 mg ustekinumab-kfce, histidine, L-histidine monohydrochloride monohydrate (1 mg), Polysorbate 80 (0.04 mg), and sucrose (76 mg). Hydrochloric acid and sodium hydroxide are used to adjust pH to 5.7- 6.3 during manufacturing. YESINTEK for Intravenous Infusion Available as 130 mg of ustekinumab-kfce in 26 mL, supplied as a single-dose Type I glass vial with a coated stopper. Each 26 mL vial delivers 130 mg ustekinumab-kfce, edetate disodium (0.47 mg), histidine (20 mg), L-histidine hydrochloride monohydrate (27 mg), methionine (10.4 mg), Polysorbate 80 (10.4 mg), and sucrose (2210 mg). Hydrochloric acid and sodium hydroxide added to adjust the pH to 5.7- 6.3 during manufacturing.
⚠️ Warnings
• Caution should be exercised in patients with history of infection, tuberculosis (TB), cancer, nerve disorder called reversible posterior leukoencephalopathy syndrome (RPLS), poor immunity, flu-like symptoms, received a vaccine, any allergy, who are taking other medications, during pregnancy and breastfeeding.
• TB skin test should be performed before using this medication.
• Avoid contact with people who infections that can be spread to others.
• Avoid live vaccination during the treatment period.
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Patient may develop increased risk of infections. If it is so consult with your healthcare provider.
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It may increase the risk of malignancy.