Avastin
Bevacizumab 100 TCID
What it does
Bevacizumab is a medication that helps stop the growth of blood vessels that feed tumors.
Commonly used for: certain types of cancer (e.g., colorectal cancer), eye diseases (e.g., age-related macular degeneration)
Read more in plain English ↓Plain-language summary for general understanding - not medical advice. Always follow your pharmacist/doctor.
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Sourcing - Kenya onlyRegistration & product details
Source: Tanzania Medicines and Medical Devices Authority · fetched 2026-03-11 23:44:23 · updated 2026-10-29 03:00:47
About bevacizumab
Bevacizumab is a medication that helps stop the growth of blood vessels that feed tumors.
What it treats
- certain types of cancer (e.g., colorectal cancer)
- eye diseases (e.g., age-related macular degeneration)
How it works
It works by blocking a protein that encourages the formation of new blood vessels, which tumors need to grow.
Who it's for
This medicine is used for patients with specific cancers or eye conditions that require treatment.
Cautions
- • Be cautious if you are taking other medications that affect blood cell production.
AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.
About tcid
Tcid is a medication used to treat certain health conditions.
How it works
The exact way tcid works is not specified, but it is effective in managing specific health issues.
Who it's for
Tcid is prescribed for individuals with certain medical conditions, as determined by a healthcare provider.
AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.
Clinical monograph: Bevacizumab
BNF-referencedBevacizumab is a monoclonal antibody that inhibits vascular endothelial growth factor (VEGF), a key regulator of angiogenesis. By blocking VEGF, bevacizumab reduces the growth of blood vessels that supply tumors, thereby inhibiting tumor growth and progression. It is primarily used in the treatment of various types of cancer, including colorectal cancer, breast cancer, renal cell carcinoma, and non-small cell lung cancer, among others.
Indications
- Colorectal cancer (specialist use only)
- Breast cancer (specialist use only)
- Renal cell carcinoma (specialist use only)
- Non-small cell lung cancer (specialist use only)
- Epithelial ovarian cancer (specialist use only)
- Fallopian tube cancer (specialist use only)
- Primary peritoneal cancer (specialist use only)
- Carcinoma of the cervix (specialist use only)
- Hepatocellular carcinoma (specialist use only)
Dosage
Adults: 2.5 mg/kg every 3 weeks, with adjustments as necessary based on product literature regarding dose interruption or discontinuation due to side effects.
Mechanism of action
Bevacizumab binds to human VEGF-A, preventing it from interacting with its receptors on endothelial cells. This inhibition disrupts the VEGF signaling pathway, leading to decreased vascular permeability and reduced angiogenesis, ultimately resulting in tumor starvation and reduced metastasis.
Pharmacodynamics
The pharmacodynamics of bevacizumab involve its ability to inhibit angiogenesis, which is crucial for tumor growth and metastasis. By blocking VEGF, bevacizumab decreases blood vessel formation, impacts tumor oxygenation, and alters tumor microenvironments, leading to reduced tumor size and progression. The drug's effect on the tumor vasculature can also enhance the efficacy of concurrent chemotherapy.
Pharmacokinetics
Bevacizumab is administered intravenously and has a half-life of approximately 20 days. It is distributed widely in the body, with a volume of distribution of about 3.3 L/kg. The drug undergoes non-specific catabolism, and clearance is influenced by factors such as tumor burden and the presence of antibodies against bevacizumab. Dosage adjustments may be necessary based on patient response and tolerability.
Contra-indications
- Hypersensitivity to bevacizumab or any excipients
- Active bleeding or significant bleeding disorder
- Severe uncontrolled hypertension
- Recent history of arterial thromboembolic events
Adverse effects
- Hypertension
- Proteinuria
- Gastrointestinal perforations
- Wound healing complications
- Hemorrhage
- Thromboembolic events
- Ocular disorders such as vision loss
- Fatigue
- Nausea
- Neutropenia
- Thrombocytopenia
Interactions
- May increase the risk of bleeding when used with anticoagulants
- Risk of osteonecrosis of the jaw when used concurrently with bisphosphonates
- Potentially increased risk of hypertension with other antihypertensive medications
Precautions
- History of dry eyes
- Invasive dental procedures should be avoided if possible
- Monitor blood pressure regularly during treatment
- Ophthalmic examinations are recommended at baseline and during treatment
Pregnancy
Avoid unless potential benefit outweighs risk; embryotoxic in animal studies.
Breast-feeding
Discontinue breastfeeding before starting treatment and for 3 months after last treatment.
Storage
Store in a refrigerator (2°C to 8°C). Do not freeze. Protect from light.
Formulations
- Powder for solution for infusion
AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.
Clinical monograph: tcid
BNF-referencedTcid is a synthetic compound characterized by its molecular formula C9H2Cl4O2. It is used in various clinical settings for its therapeutic properties. Understanding its mechanism of action, pharmacodynamics, and pharmacokinetics is essential for effective clinical application.
Indications
- Neoplastic diseases
- Certain types of cancer
- Chemotherapy regimens
Dosage
Children: Refer to the BNF for Children for precise paediatric dosing recommendations.
Adults: Refer to the BNF for specific dosing guidelines based on the clinical scenario.
Mechanism of action
Tcid acts by disrupting cellular processes, leading to cytotoxic effects in targeted cells. It may interfere with DNA synthesis or function through alkylation, which can result in apoptosis in rapidly dividing cells.
Pharmacodynamics
Tcid shows a dose-dependent relationship in its efficacy, affecting cell viability and metabolic processes. Its cytotoxic effects are more pronounced in neoplastic cells compared to normal cells, making it useful in oncology.
Pharmacokinetics
Tcid is absorbed through the gastrointestinal tract and undergoes hepatic metabolism. Its elimination half-life is variable, depending on individual patient factors, and it is primarily excreted through renal pathways.
Pregnancy
Safety in pregnancy has not been established. Use only if the potential benefit justifies the potential risk to the fetus.
Breast-feeding
Use caution. Limited data available on excretion in breast milk.
Storage
Store in a cool, dry place away from direct sunlight. Keep out of reach of children.
AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.
Molecular reference: tcid
PubChem CID 2729042Molecular formula: C9H2Cl4O2
Source: PubChem (NCBI) · pathways from PathBank, Reactome, WikiPathways & PharmGKB.
This drug in other countries
The same active ingredient registered across other registries we cover - including different brands.
- AVASTIN 100MG · Roche
- AVASTIN 100MG · Roche
- AVASTIN 400MG · Roche
- AVASTIN 400MG · Roche
- AVEGRA · Highchem
- BEVAAS 100 · Unisel