The Contents Which Every Drug Monograph Should Contain

The Contents Which Every Drug Monograph Should Contain Introduction: A drug, when launched, goes through a series of medical tests by different medical associations. The tests’ findings are compiled on a report, and the ingredients inside the drug are printed on the label of the medicine. This, in scientific terms, is known as Drug monograph. Along with the information on components of the medication, a monograph also contains its effects, side effects, dosage, appearance, and usage of the drug. There is a particular drug monograph format that the manufacturers should follow. This article goes through the details of the contents present in a drug monograph.

Drug Monograph Format: The drug monograph should publish the name of the institution as the heading. Then it has to mention the generic name of the drug, like the name used in standard terms. The trade brand name should come next in the format. If the brand has specific contact details like a website, then it can be mentioned too. Next, the therapeutic category and the drug classification should be added to the drug monograph template.

Classifications to Add: Different types of classification can be added at this point. The AHFS Number and classification of the drug can be used by determining the most appropriate ranking of the drug on the list of AHFS Drug Information book. FDA Classification of the drug is also essential, which can be added by FDA website approval. The status of the drug (prescription, nonprescription,

Other Important Additions: The list of conventional treatments of similar indications of the drug should be added to the drug monograph template. A. After this, the recommendations and signs of this drug for the patients should be written on the monograph.

After this, Pharmacological Data (Bacterial spectrum and Action mechanism) and Therapeutic Indications of the drug should be added. The information on how this particular drug and similar drugs can fit the clinical guidelines and the potential unlabeled usages should be mentioned. At the end of the drug monograph format, the clinical comparison of the particular drug with at least two medical studies should be mentioned.

In case supportive studies of the indication of the drug are found, one should also add them to the monograph. The reviews should be covered thoroughly, and all the shortcomings and recommendations regarding the drug should be mentioned on the drug monograph template.

Here, the pharmacogenomic information of the drug can also be added.

Search Terms: drug monograph format, drug monograph template