Leaflet TEMSIROLIMUS ACCORD 30mg concentrate+solvent for solution for infusion


Indicated for: cancer

Route of administration: infusion

Substance: temsirolimus (antineoplastic agent)

ATC: L01EG01 (Antineoplastic and immunomodulating agents | Protein kinase inhibitors | Mammalian target of rapamycin (MTOR) kinase inhibitors)

Temsirolimus is an mTOR (mammalian target of rapamycin) inhibitor used for the treatment of advanced renal cancer and other types of tumors. It works by inhibiting the growth and proliferation of tumor cells, thereby reducing disease progression.

The medication is administered via intravenous infusion, usually once a week, as directed by a doctor. It is important for patients to be closely monitored during treatment to prevent potential complications.

Patients should be aware of potential side effects, such as skin rashes, fatigue, or elevated blood glucose levels. It is important to inform the doctor of any unusual symptoms.

Common side effects include skin rashes, fatigue, nausea, and increased cholesterol or glucose levels. In rare cases, severe reactions such as serious infections or kidney failure may occur. Patients should be informed of these risks before starting treatment.

General data about TEMSIROLIMUS ACCORD 30mg

  • Substance: temsirolimus
  • Date of last drug list: 01-09-2021
  • Commercial code: W67928001
  • Concentration: 30mg
  • Pharmaceutical form: concentrate+solvent for solution for infusion
  • Quantity: 1
  • Product type: generic
  • Prescription restrictions: P-RF - Medicines prescription that is retained in the pharmacy (not renewable).

Marketing authorisation

  • Manufacturer: ACCORD HEALTHCARE POLSKA SP. Z. O.O. - POLONIA
  • Holder: ACCORD HEALTHCARE POLSKA SP. Z.O.O. - POLONIA
  • Number: 13948/2021/01
  • Shelf life: 3 years-after packing for marketing;dupa diluare-it is used immediately

Concentrations available for temsirolimus

  • 25mg/ml
  • 30mg