E Rubilee
E Rubilee Uses, Dosage, Side Effects, Food Interaction and all others data.
E Rubilee, 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.
E Rubilee is an antineoplastic in the anthracycline class. General properties of drugs in this class include: interaction with DNA in a variety of different ways including intercalation (squeezing between the base pairs), DNA strand breakage and inhibition with the enzyme topoisomerase II. Most of these compounds have been isolated from natural sources and antibiotics. However, they lack the specificity of the antimicrobial antibiotics and thus produce significant toxicity. The anthracyclines are among the most important antitumor drugs available. Doxorubicin is widely used for the treatment of several solid tumors while daunorubicin and idarubicin are used exclusively for the treatment of leukemia. E Rubilee may also inhibit polymerase activity, affect regulation of gene expression, and produce free radical damage to DNA. E Rubilee possesses an antitumor effect against a wide spectrum of tumors, either grafted or spontaneous. The anthracyclines are cell cycle-nonspecific.
| Trade Name | E Rubilee |
| Availability | Prescription only |
| Generic | Epirubicin |
| Epirubicin Other Names | 4'-Epiadriamycin, Epiadriamycin, Epirubicin, Epirubicina, Epirubicine, Epirubicinum, Pidorubicina, Pidorubicine, Pidorubicinum |
| Related Drugs | tamoxifen, letrozole, paclitaxel, Femara, Herceptin, Soltamox |
| Type | Injection |
| Formula | C27H29NO11 |
| Weight | Average: 543.5193 Monoisotopic: 543.174060775 |
| Protein binding | 77% |
| Groups | Approved |
| Therapeutic Class | Cytotoxic Chemotherapy |
| Manufacturer | Admac Formulations |
| Available Country | India |
| Last Updated: | September 19, 2023 at 7:00 am |
Uses
E Rubilee Injection is an anthracycline topoisomerase II inhibitor used as a component of adjuvant therapy in patients with evidence of axillary node tumor involvement following resection of primary breast cancer
E Rubilee is also used to associated treatment for these conditions: Breast Cancer, Breast Cancer Stage II, Breast Cancer Stage III, Colorectal Cancers, Hormone Refractory Prostate Cancer, Non-Small Cell Lung Carcinoma (NSCLC), Ovarian Cancer, Papillary transitional cell carcinoma of bladder, Recurrent Superficial Bladder Cancer, Small Cell Lung Cancer (SCLC), Soft Tissue Sarcoma (STS), Stomach Tumor, Carcinoma in situ of urinary bladder
How E Rubilee works
E Rubilee has antimitotic and cytotoxic activity. It inhibits nucleic acid (DNA and RNA) and protein synthesis through a number of proposed mechanisms of action: E Rubilee forms complexes with DNA by intercalation between base pairs, and it inhibits topoisomerase II activity by stabilizing the DNA-topoisomerase II complex, preventing the religation portion of the ligation-religation reaction that topoisomerase II catalyzes. It also interferes with DNA replication and transcription by inhibiting DNA helicase activity.
Dosage
E Rubilee dosage
Acute leukaemias; Lymphoma; Multiple myeloma; Solid tumours:
- 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.
Adjuvant treatment in axillary-node positive breast cancer: Recommended starting doses: 100-120 mg/m2 as a single dose on day 1 or as 2 divided doses on days 1 and 8 of each 28-day cycle. Repeat for 6 cycles.
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 Effects
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.
Toxicity
bone marrow aplasia, grade 4 mucositis, and gastrointestinal bleeding
Precaution
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
Interaction
Paclitaxel and other anthracyclines. Cimetidine, heparin. Antineoplastic drugs, cardiotoxic drugs, radiation, hepatoactive drugs.
Food Interaction
- Drink plenty of fluids. Increased fluid intake increases urine output and the excretion of uric acid.
E Rubilee Alcohol interaction
[Moderate]
The concomitant or sequential use of epirubicin with agents known to induce hepatotoxicity may potentiate the risk of liver injury.
E Rubilee undergoes elimination through the hepatobiliary system.
Caution and clinical and laboratory monitoring for signs of liver injury are advisable before, during, or after use of epirubicin with other agents that are potentially hepatotoxic.
E Rubilee Drug Interaction
Moderate: amoxicillin / clavulanate, amoxicillin / clavulanate, ethanol, ethanol, acetaminophen, acetaminophen, tramadol, tramadol, valproic acid, valproic acidUnknown: paclitaxel protein-bound, paclitaxel protein-bound, aspirin, aspirin, amoxicillin, amoxicillin, aprepitant, aprepitant, esomeprazole, esomeprazole
E Rubilee Disease Interaction
Major: heart disease/toxicity, liver disease, neutropeniaModerate: myelosuppression/infection, renal impairment
Volume of Distribution
- 21 ± 2 L/kg [60 mg/m2 Dose]
- 27 ± 11 L/kg [75 mg/m2 Dose]
- 23 ± 7 L/kg [120 mg/m2 Dose]
- 21 ± 7 L/kg [150 mg/m2 Dose]
Elimination Route
100%
Half Life
Half-lives for the alpha, beta, and gamma phases of about 3 minutes, 2.5 hours and 33 hours, respectively
Clearance
- 65 +/- 8 L/hour [Patients1 with Solid Tumors Receiving Intravenous E Rubilee 60 mg/m2]
- 83 +/- 14 L/hour [Patients1 with Solid Tumors Receiving Intravenous E Rubilee 75 mg/m2]
- 65 +/- 13 L/hour [Patients1 with Solid Tumors Receiving Intravenous E Rubilee 120 mg/m2]
- 69 +/- 13 L/hour [Patients1 with Solid Tumors Receiving Intravenous E Rubilee 150 mg/m2]
Elimination Route
E Rubilee and its major metabolites are eliminated through biliary excretion and, to a lesser extent, by urinary excretion.
Pregnancy & Breastfeeding use
Discontinue nursing prior to taking E Rubilee. Not known if excreted in breast milk
Contraindication
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.
Innovators Monograph
You find simplified version here E Rubilee
E Rubilee contains Epirubicin see full prescribing information from innovator E Rubilee Monograph, E Rubilee MSDS, E Rubilee FDA label
FAQ
What is E Rubilee used for?
E Rubilee is an anthracycline drug used for chemotherapy. E Rubilee is used in combination with other medications to treat breast cancer in patients who have had surgery to remove the tumor.
How safe is E Rubilee?
E Rubilee may increase your risk for developing leukemia (cancer of the white blood cells), especially when it is given in high doses or together with certain other chemotherapy medications. E Rubilee can cause a severe decrease in the number of blood cells in your bone marrow.
How does E Rubilee work?
E Rubilee works by slowing or stopping the growth of cancer cells in your body.
What are the common side effects of E Rubilee?
Common side effects of E Rubilee are include;
- Black, tarry stools
- bleeding, redness, or ulcers in the mouth or throat
- chest pain
- cough or hoarseness
- fever or chills
- lower back or side pain
- pain or burning in the mouth or throat
- painful or difficult urination
- sore throat
- sores, ulcers, or white spots in the mouth or on the lips
- swollen glands
- trouble breathing
- unusual bleeding or bruising
- unusual tiredness or weakness
Is E Rubilee safe during pregnancy?
Use is contraindicated. US FDA pregnancy category: Not assigned. Risk Summary: Based on findings from animal studies and its mechanism of action, this drug can cause fetal harm when administered to a pregnant woman.
Is E Rubilee safe during breastfeeding?
Use is contraindicated. Because of the potential for serious adverse reactions in the breastfed child, advise lactating women not to breastfeed during therapy and for at least 7 days after.
Can I drink alcohol with E Rubilee?
Frequent or heavy alcohol consumption during chemotherapy is generally a bad idea. One reason for this is that alcohol can worsen some chemotherapy side effects, such as dehydration, diarrhea, and mouth sores. Additionally, alcohol and chemotherapy drugs are both processed by the liver.
Can I drive after taking E Rubilee?
If you have any of these symptoms, do not drive, operate machinery, or do anything else that could be dangerous. Be careful when drinking alcohol while you are taking this medicine. If you drink alcohol, dizziness or light- headedness may be worse.
How do I take E Rubilee?
E Rubilee comes as a solution (liquid) to be injected intravenously (into a vein) by a doctor or nurse in a medical facility along with other chemotherapy medications.
How long does E Rubilee take to work?
It can take up to 30 minutes if you have it on its own but it might take longer if you have it with other drugs. For bladder cancer, you might have E Rubilee every week, for up to 8 weeks.
How long does E Rubilee stay in my system?
This medicine may turn your urine red for 1 or 2 days after your treatment.
How long can I take E Rubilee?
Chemotherapy is often given for a specific time, such as 6 months or a year.
Who should not take E Rubilee?
You should not use E Rubilee if you have an untreated or uncontrolled infection, severe liver disease, severe heart problems, or if you have recently had a heart attack. You may not be able to use E Rubilee if you have already been treated with a certain amount of other cancer medications. You should not use this medication if you are allergic to E Rubilee or similar medications.
What happens if I miss a dose?
Call your doctor for instructions if you miss an appointment for your E Rubilee injection.
What happen if I overdose on E Rubilee?
If you've taken more than the recommended amount of a drug or enough to have a harmful effect on your body's functions, you have overdosed. An overdose can lead to serious medical complications, including death.
Can E Rubilee affect my heart?
E Rubilee can cause dangerous effects on your heart that may not be reversible and could occur months to years after you receive E Rubilee.
Can E Rubilee cause fertility problems?
E Rubilee can stop your ovaries from working. This causes infertility, which can be temporary or permanent. It can also bring on the menopause.
Is E Rubilee an irritant?
E Rubilee should be administered only into a vein. However, it may leak into surrounding tissue causing severe irritation or damage.
