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Compounding as an ADR Mechanism in Intellectual Property DisputesThe Kenyan Experience under the AntiCounterfeit ActPresented during WIPOs ACE 17th Session, February 46 2025, GenevaRobi Mbugua Njoroge,
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01
Gather all necessary information: Identify the medication that needs to be compounded.
02
Verify the prescription: Ensure the prescription is clear and that you have all required details.
03
Assemble ingredients: Collect all active and inactive ingredients required for the compounding process.
04
Use proper equipment: Ensure you have the appropriate tools and equipment for measuring and mixing the compounds.
05
Calculate dosage: Accurately calculate the dosage and proportions of each ingredient based on the prescription.
06
Mix ingredients: Follow the specific compounding formula to mix the ingredients thoroughly.
07
Quality check: Perform a quality check to ensure consistency and accuracy of the compound.
08
Label properly: Create a label for the compounded medication with all necessary information including patient name, dosage, and instructions.
09
Document the process: Keep detailed records of the compounding process for future reference.

Who needs compounding as an?

01
Patients with allergies to certain ingredients found in commercial medications.
02
Individuals requiring specific dosage forms (liquid, cream, or gel) not available in standard pharmaceuticals.
03
Pediatric patients needing tailored dosages or flavoring for better compliance.
04
Patients requiring medication strength adjustments due to individual health conditions.
05
Individuals needing discontinued medications that require compounding to create alternatives.
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Compounding is the process of combining various ingredients or components to create a final product, often utilized in pharmaceuticals to tailor medications for individual patient needs.
Generally, pharmacists, pharmaceutical companies, and healthcare providers who prepare compounded medications or products are required to file for compounding.
Filling out compounding documents typically requires detailed information about the ingredients, quantities, preparation methods, and labeling; it may involve following specific guidelines set by regulatory authorities.
The purpose of compounding is to customize medications to meet the unique needs of patients, such as altering dosage forms, flavors, or eliminating allergens.
Required information may include the name and strength of the compounded formulation, ingredients and their sources, compounding date, prescribed dosage, patient information, and any special instructions.
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