Altering, mixing, or combining ingredients of a drug in order to create a medicine which is customized to the needs of a patient is known as compounding. This process is done by a pharmacist or physician who is licensed. In the event that the drug to be compounded it outsourced to another practitioner or facility, it has to be produced under the supervision of a pharmacist which is licensed. This practice is currently on the raise. When in search of Compounding Pharmacies Ocala FL should be given priority.
The primary responsibility of pharmacists in the 50s and 60s was to compound drugs for patients. Patients went into the pharmacy with a prescription from a doctor and the pharmacist would produce a preparation that was tailored towards specific needs that the patient had. However, when mass production of drugs began, the role of pharmacists was taken over by the companies.
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.
The second reason is that, the aged and small children may have difficulties swallowing big tablets of drugs. A similar case applies to pets that are unable to swallow drugs. Such issue may be tackled by providing a compounded alternative. The liquid form of the drug may be the alternative. The liquid drug can then be taken easily by the patient. Compounded drugs can also be in form of lotions and creams.
In the US, compounded drugs do not have the approval of the FDA. This is because the safety and effectiveness of the preparations cannot be ascertained by the FDA. However, to ensure quality and safety, all manufacturing processes are governed by strict regulations and standards. Before the preparations are marketed, they must meet certain standards in their process of production as well the product themselves.
Oversight and supervision of compounding pharmacies rests with the state boards of pharmacy in every jurisdiction. FDA retains certain authority over operations despite state boards having full responsibility over these establishments within their jurisdictions. FDA oversees and has direct regulation over every outsourcing facility. A part from regular inspection by FDA outsourcing facilities operates in compliance of various requirements.
Because compounded drugs are not approved by the FDA, it is possible that they may pose some health risks. This is because the practices applied in production are of poor quality in some cases. The ingredients used may also be contaminated. The drugs are also likely to be ineffective, which means that patients get to use products that have not been approved based on safety and effectiveness.
The primary responsibility of pharmacists in the 50s and 60s was to compound drugs for patients. Patients went into the pharmacy with a prescription from a doctor and the pharmacist would produce a preparation that was tailored towards specific needs that the patient had. However, when mass production of drugs began, the role of pharmacists was taken over by the companies.
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.
The second reason is that, the aged and small children may have difficulties swallowing big tablets of drugs. A similar case applies to pets that are unable to swallow drugs. Such issue may be tackled by providing a compounded alternative. The liquid form of the drug may be the alternative. The liquid drug can then be taken easily by the patient. Compounded drugs can also be in form of lotions and creams.
In the US, compounded drugs do not have the approval of the FDA. This is because the safety and effectiveness of the preparations cannot be ascertained by the FDA. However, to ensure quality and safety, all manufacturing processes are governed by strict regulations and standards. Before the preparations are marketed, they must meet certain standards in their process of production as well the product themselves.
Oversight and supervision of compounding pharmacies rests with the state boards of pharmacy in every jurisdiction. FDA retains certain authority over operations despite state boards having full responsibility over these establishments within their jurisdictions. FDA oversees and has direct regulation over every outsourcing facility. A part from regular inspection by FDA outsourcing facilities operates in compliance of various requirements.
Because compounded drugs are not approved by the FDA, it is possible that they may pose some health risks. This is because the practices applied in production are of poor quality in some cases. The ingredients used may also be contaminated. The drugs are also likely to be ineffective, which means that patients get to use products that have not been approved based on safety and effectiveness.
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