Epirubicin Sandoz
Epirubicin Hydrochloride → (9 brands)
10 mg vial
৳ 783.06,50
mg vial৳ 3,537.77
SANDOZ (A Novartis Division)
Drug Class
Cytotoxic Chemotherapy
Indication
Stomach carcinoma
Dosage Form
IV Infusion
Manufacturer
SANDOZ (A Novartis Division)
Compare Alternate Brands
Same generic (Epirubicin Hydrochloride), 2 mg/ml, IV Infusion — 8 alternate brands available.
Lowest
Epicin
Techno Drugs Ltd.
৳ 850.00,50
10 mg vial
Epiruba
Drug International Ltd.
৳ 3,600.00
50 mg vial
Epirubicin PhaRes
Pharma Resources
৳ 1,420.00,50
10 mg vial
Epirubin
Healthcare Pharmaceuticals Ltd.
৳ 3,700.00
50 mg vial
Episindan
BOTS Pvt. Limited
৳ 915.00,50
10 mg vial
Erubin
Beacon Pharmaceuticals Ltd.
৳ 915.00,50
10 mg vial
Indication DetailsView
Epirubicin Injection is an anthracycline topoisomerase II inhibitor indicated as a component of adjuvant therapy in patients with evidence of axillary node tumor involvement following resection of primary breast cancer
Therapeutic ClassView
Cytotoxic Chemotherapy
PharmacologyView
Epirubicin, an anthracycline with cytotoxic properties. It inhibits DNA and RNA synthesis by steric obstruction after intercalating between DNA base pairs that triggers DNA cleavage by by topoisomerase II. It also inhibits DNA helicase and generates cytotoxic free radicals.
DosageView
Acute leukaemias; Lymphoma; Multiple myeloma; Solid tumours:
Intravesical Local treatment of bladder carcinoma: As 0.1% soln: 50 mg/wk for 8 wk; reduce dose if chemical cystitis develops.
For carcinoma in-situ: 80 mg in 50 mL wkly.
For prevention of recurrence in patients who have undergone transurethral resection: 50 mg/wk for 4 wk, followed by 50 mg/mth for 11 mth; retain soln in the bladder for 1 hr during each administration.
- As a single agent: 60-90 mg/m2 3-4 wkly.
- Max (total cumulative dose): 0.9-1 g/m2.
- Palliative care: 12.5-25 mg/m2 once wkly.
Intravesical Local treatment of bladder carcinoma: As 0.1% soln: 50 mg/wk for 8 wk; reduce dose if chemical cystitis develops.
For carcinoma in-situ: 80 mg in 50 mL wkly.
For prevention of recurrence in patients who have undergone transurethral resection: 50 mg/wk for 4 wk, followed by 50 mg/mth for 11 mth; retain soln in the bladder for 1 hr during each administration.
Side EffectsView
In early breast cancer, acute adverse events occurring in ≥10% of patients are leucopenia, neutropenia, anemia, thrombocytopenia, amenhorrhea, lethargy, nausea/vomiting, mucositis, diarrhea, infection, conjunctivitis/keratitis, alopecia, local toxicity and rash/itch.
Long term adverse events occurring at a frequency of 1-2% are asymptomatic drops in LVEF and CHF and secondary leukemia.
Long term adverse events occurring at a frequency of 1-2% are asymptomatic drops in LVEF and CHF and secondary leukemia.
ContraindicationsView
Cardiac impairment, severe or recent Ml; previous full cumulative doses of anthracyclines. Hypersensitivity; severe hepatic dysfunction. Not for intravesical use where invasive tumours have penetrated the bladder wall; urinary infections, bladder inflammation or catheterisation problems. Pregnancy, lactation.
PrecautionsView
Previous extensive radiotherapy, bone infiltration by tumour, severe renal and hepatic dysfunction. May cause tumor lysis syndrome or radiation recall. Elderly women >70 yr. CV disease, hypertensive cardiomyopathy; monitor hematological and cardiac function regularly. Extravasation during IV admin may result in severe local tissue necrosis. Do not give via IM/SC routes as extravasation can lead to severe local necrosis
InteractionsView
Paclitaxel and other anthracyclines. Cimetidine, heparin. Antineoplastic drugs, cardiotoxic drugs, radiation, hepatoactive drugs.
Pregnancy & LactationView
Discontinue nursing prior to taking Epirubicin. Not known if excreted in breast milk