Compounding is the combining, mixing, or altering the ingredients in a drug so as to create a medication that is tailored to the specific needs of individual patients. It is a process that is done by licensed physicians or pharmacists. If the compounded drug is outsourced to another facility or practitioner, it must be produced under the direct supervision of a licensed pharmacist. This practice is becoming increasingly popular today. When one needs Compounding Pharmacies Ocala FL offers the perfect location to visit.
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.
There is a variety of reasons why compounded drugs may be more suitable for certain patients. The first reason is when one has an individualized problem that cannot be addressed by a drug that is available on the market commercially. For instance, one may need a commercial drug, but because of an allergy to some of the components of the drug, they cannot use it. Thus, excluding the cause of allergy in the compounded drug solves the problem.
Secondly, small children or elderly citizens may find it hard to swallow large tablets of drugs. The same case often applies to pets, which cannot swallow drugs. This can be solved by providing a compounded alternative, which may be in the form of a liquid. The patient or pet can then drink the liquid with more ease. Besides liquids, compounded drugs may also be made in the form of creams or lotions.
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.
Oversight and direct supervision of compounding pharmacies is a responsibility assumed by state boards of pharmacy. Even with state boards taking jurisdiction over these facilities, the FDA also has some say in what they do in some cases. For instance, all outsourcing facilities remain under the oversight and regulation of the FDA. They have to comply with regular inspections as well as set standards.
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.
There is a variety of reasons why compounded drugs may be more suitable for certain patients. The first reason is when one has an individualized problem that cannot be addressed by a drug that is available on the market commercially. For instance, one may need a commercial drug, but because of an allergy to some of the components of the drug, they cannot use it. Thus, excluding the cause of allergy in the compounded drug solves the problem.
Secondly, small children or elderly citizens may find it hard to swallow large tablets of drugs. The same case often applies to pets, which cannot swallow drugs. This can be solved by providing a compounded alternative, which may be in the form of a liquid. The patient or pet can then drink the liquid with more ease. Besides liquids, compounded drugs may also be made in the form of creams or lotions.
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.
Oversight and direct supervision of compounding pharmacies is a responsibility assumed by state boards of pharmacy. Even with state boards taking jurisdiction over these facilities, the FDA also has some say in what they do in some cases. For instance, all outsourcing facilities remain under the oversight and regulation of the FDA. They have to comply with regular inspections as well as set standards.
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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