adovr_d87389c80da99bef8f38776d3f905184 Articles medical and health: Information On Ocala Compounding Pharmacy

Information On Ocala Compounding Pharmacy

By Virginia Olson


The science or process of making individualized medication for individual use is referred to as pharmaceutical compounding. In this process, ingredients from various medications are combined, altered, or mixed to produce a single drug that can meet the specific needs of an individual. The process is undertake by a licensed pharmacists or someone who is not a pharmacist, but under the supervision of a licensed pharmacist. Prescriptions for medications like that must be given by a certified medical practitioner. Any Ocala compounding pharmacy has the necessary certification and licensure needed to operate within the state.

The term compounding is only used on processes that involve mixing or combining several drugs to produce a single medication. Different reasons make it necessary for a patient to require compounded medication. For starters, one may need such medication if they do not get affected in the required manner by conventional medication. An instance like that is where one exhibits allergic reaction to certain components making up a given medication.

Compounded medications are often tailored to accommodate the specific requirements of the patient. For that reason, they are not FDA-approved. That means that their safety and effectiveness is not verified by the FDA. The drug approval process is relied upon by patients and physicians to ensure the effectiveness and safety of products. Drug approval process exists to make sure that operations are standardized according to federal laws.

Normally, it is the responsibility of state boards of pharmacy to ensure that state-licensed compounding pharmacies observe set standards in all operations they undertake. However, the FDA continues to continues to exert a certain degree of influence on the establishments too. Outsourcing facilities are usually subjected to stricter regulation by the FDA. Outsourcing facilities need to be inspected by FDA inspectors on a risk-based schedule.

These facilities continue to have certain health risks associated with their operations, products, and services, which are not in compliance with federal quality standards. To start with, there are cases of drugs being made using poor quality practices, which makes the contaminated, adulterated, or sub- or super-potent. Another risk emanates from the fact that patients are more likely to use drugs that are compounded in place of FDA-approved medications.

Drugs that are compounded today are much better, safer, and more effective because of advancements in technology. A lot of revolution and standardization have occurred in the field because of technological developments. Currently, pharmacists are in a position to be very specific in their preparations in terms of dosages, flavors, strengths, and ingredients in their medications.

Several years ago, compounding was the technique used for the production of all prescribed medications. This changed when mass production of drugs began in the 50s and 60s. The traditional roles of pharmacists changed from preparing drugs to dispensing mass-produced drugs. Even training on drug preparation only existed to a limited level.

However, mass production did not satisfy the needs of everybody. Some people had their needs not met because they need custom tailored medications. That returned compounding pharmacies into business. Today, federal regulations state that these facilities must at any given time have a licensed pharmacist onsite.




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