Drug compounding refers to the process of mixing, altering, or combining ingredients composed in a drug for the purpose of creating medication that would address specific needs of an individual patient. Only licensed pharmacists of physicians are allowed to undertake this process. If the production is happening in an outsourcing facility, supervision must be provided by a licensed pharmacist. When in need of Compounding Pharmacies Ocala FL should be visited.
Before the 195o and 1960s, pharmacists had the primary role of producing compounded drugs. They received prescriptions from a medical practitioner and compounded drugs to suit the specific needs of their patients. However, this changed when drugs began to be produced in masses in the 50s and 60s. With mass production of drugs, the role of pharmacists changed.
They changed to dispensing drugs to patients according to their perceptions as they no longer compounded drugs. Training schools also stopped training them in compounding drugs and shifted focus to other areas. Unfortunately, it was realized that mass production of drugs failed to address all needs of patients. This meant that pharmacists had to go back to the practice of compounding drugs.
Patients need compounded drugs for a variety of reasons. First, the patient might have medical needs that cannot be met by the drug that is currently commercially-available on the market. For instance, a patient might has an allergy that prevents them from using the commercial drug on the market. This may be caused by the presence of certain ingredients in the drug that cause the allergy. Elimination of the unwanted ingredient may solve the problem.
Secondly, there are certain people who may have problems with taking drugs in solid form. Such groups of people include children and the elderly. It may also be hard to administer tablets to pets and other animals. Thus, changing the form of the medications to liquids helps solve this problem. Other forms include lotions and creams.
Compounded drugs do not have FDA approval in the US. The approval is denied because it is hard for FDA to verify the safety and effectiveness of such drugs. Despite this, there are standards governing the manufacturing process of compounded drugs to ensure quality and safety. Before being marketed to the public all compounded drugs must fulfill these standards.
The state boards of pharmacy are responsible for direct supervision and oversight of compounding pharmacies within their jurisdictions. Although state boards have full responsibility and jurisdiction over these establishments, the FDA also retains some authority over the operations. However, all outsourcing facilities are under the direct regulation and oversight of the FDA. They are required to comply with various requirements besides being inspected by the FDA regularly.
There may be some health risks associated with compounded drugs since they do not have FDA approval. The use of poor quality practices is one of the causes of possible risks. Also, use of contaminated ingredients is a possibility. The efficiency of the preparation is often questionable, given that they are not researched and approved for efficiency and safety.
Before the 195o and 1960s, pharmacists had the primary role of producing compounded drugs. They received prescriptions from a medical practitioner and compounded drugs to suit the specific needs of their patients. However, this changed when drugs began to be produced in masses in the 50s and 60s. With mass production of drugs, the role of pharmacists changed.
They changed to dispensing drugs to patients according to their perceptions as they no longer compounded drugs. Training schools also stopped training them in compounding drugs and shifted focus to other areas. Unfortunately, it was realized that mass production of drugs failed to address all needs of patients. This meant that pharmacists had to go back to the practice of compounding drugs.
Patients need compounded drugs for a variety of reasons. First, the patient might have medical needs that cannot be met by the drug that is currently commercially-available on the market. For instance, a patient might has an allergy that prevents them from using the commercial drug on the market. This may be caused by the presence of certain ingredients in the drug that cause the allergy. Elimination of the unwanted ingredient may solve the problem.
Secondly, there are certain people who may have problems with taking drugs in solid form. Such groups of people include children and the elderly. It may also be hard to administer tablets to pets and other animals. Thus, changing the form of the medications to liquids helps solve this problem. Other forms include lotions and creams.
Compounded drugs do not have FDA approval in the US. The approval is denied because it is hard for FDA to verify the safety and effectiveness of such drugs. Despite this, there are standards governing the manufacturing process of compounded drugs to ensure quality and safety. Before being marketed to the public all compounded drugs must fulfill these standards.
The state boards of pharmacy are responsible for direct supervision and oversight of compounding pharmacies within their jurisdictions. Although state boards have full responsibility and jurisdiction over these establishments, the FDA also retains some authority over the operations. However, all outsourcing facilities are under the direct regulation and oversight of the FDA. They are required to comply with various requirements besides being inspected by the FDA regularly.
There may be some health risks associated with compounded drugs since they do not have FDA approval. The use of poor quality practices is one of the causes of possible risks. Also, use of contaminated ingredients is a possibility. The efficiency of the preparation is often questionable, given that they are not researched and approved for efficiency and safety.
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