Soracent 200 mg (Tablet)
Unit Price: ৳ 150.00 (3 x 10: ৳ 4,500.00)
Strip Price: ৳ 1,500.00
Medicine Details
Category | Details |
---|---|
Generic | Sorafenib tosylate |
Company | Incepta pharmaceuticals ltd |
Indications
- Unresectable hepatocellular carcinoma (HCC)
- Advanced renal cell carcinoma (RCC)
Pharmacology
- Kinase inhibitor
- Decreases tumor cell proliferation
- Inhibits multiple intracellular and cell surface kinases
- Involved in tumor cell signaling, angiogenesis, and apoptosis
Dosage & Administration
- Recommended daily dose: 400 mg tablets
- Taken twice daily without food
- Treatment duration until patient is no longer clinically benefiting or unacceptable toxicity occurs
- Management of suspected adverse drug reactions may require temporary interruption and/or dose reduction
- No dose adjustment based on patient age, gender, or body weight
- Missed doses: Skip the missed dose and take next dose at regular time. Do not double the dose
Interaction
- Contraindicated in patients with squamous cell lung cancer when combined with carboplatin and paclitaxel
- Systemic exposure to UGT1A1 and UGT1A9 substrates may increase
- Caution recommended when co-administered with Docetaxel, Doxorubicin, Fluorouracil, CYP2B6 and CYP2C8 substrates, and neomycin
- Inducers of CYP3A4 activity may decrease Soracent concentrations
Contraindications
- Severe hypersensitivity to Sorafenib or any other component of Sorafenib
- Contraindicated in patients with squamous cell lung cancer when combined with carboplatin and paclitaxel
Side Effects
- Serious adverse reactions: cardiac ischemia, infarction, hemorrhage, hypertension, hand-foot skin reaction, rash, gastrointestinal perforation, wound healing complications
Pregnancy & Lactation
- May cause fetal harm when administered to a pregnant woman
- Women of childbearing potential advised to avoid becoming pregnant
- Unknown excretion in human milk
Precautions & Warnings
- Consider discontinuation in patients developing cardiac ischemia and/or infarction
- Increased risk of bleeding, hypertension, dermatologic toxicities, and gastrointestinal perforation
- Monitor patients taking concomitant warfarin regularly
- Based on clinical judgment, resume therapy following major surgical intervention
- Use cautiously in combination with various drugs and in hepatic impairment
- Safety and effectiveness not studied in pediatric patients
- No dose adjustment required for renal impairment
Use in Special Populations
- Safety and effectiveness not studied in pediatric patients
- No differences in safety or efficacy observed between older and younger patients
- No dose adjustment required for renal impairment
- AUC may be 23-65% lower in mild to moderate hepatic impairment
Overdose Effects
- No specific treatment for Soracent overdose
- Adverse reactions include primarily diarrhea and dermatologic effects
Therapeutic Class
- Targeted Cancer Therapy
Storage Conditions
- Store below 30°C at room temperature
- Dispense in original bottle