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.
It was the primary role of pharmacists to produce compounded drugs before the 1950s and 1960s. They accepted prescriptions from other medical professionals to compound drugs that suited particular needs of patients. This practice later changed in the 50s and 60s when drugs started to be mass-produced. The duties of pharmacists had to change when mass production of drug started.
Pharmacists were no longer compounding drugs, but only dispensing them based on prescriptions held by patients. Training institutions stopped training pharmacists in the science of compounding drugs but instead focused more on other areas. However, it would soon come to be realized that the mass-produced drugs did not address the needs of all patients and pharmacists starts to compound drugs again.
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 is a possibility that compounded drugs can pose certain health risks. It is for this reason that FDA does not approve of their use. In some cases, the production line is of poor quality due to malpractices. Also, the ingredients utilized could be contaminated. Besides, these are likely to be ineffective. This implies that patients are using drugs which have not been approved on the basis of their efficiency and safety.
It was the primary role of pharmacists to produce compounded drugs before the 1950s and 1960s. They accepted prescriptions from other medical professionals to compound drugs that suited particular needs of patients. This practice later changed in the 50s and 60s when drugs started to be mass-produced. The duties of pharmacists had to change when mass production of drug started.
Pharmacists were no longer compounding drugs, but only dispensing them based on prescriptions held by patients. Training institutions stopped training pharmacists in the science of compounding drugs but instead focused more on other areas. However, it would soon come to be realized that the mass-produced drugs did not address the needs of all patients and pharmacists starts to compound drugs again.
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 is a possibility that compounded drugs can pose certain health risks. It is for this reason that FDA does not approve of their use. In some cases, the production line is of poor quality due to malpractices. Also, the ingredients utilized could be contaminated. Besides, these are likely to be ineffective. This implies that patients are using drugs which have not been approved on the basis of their efficiency and safety.
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