What is the difference between generic name and chemical name?

The chemical name is a scientific name based on the compound’s chemical structure (e.g., 6-thioguanine) and is almost never used to identify the drug in a clinical or marketing situation. The generic name is granted by the USAN Council and is commonly used to identify a drug during its useful clinical lifetime.

Why the name cholesterol busters could never be used for a drug in the US?

They do handwriting tests to catch names that might look alike when scribbled out on a prescription pad. They also reject any names that could be seen as a boast about the drug’s power or efficacy, which is why you won’t see any drugs named Cholesterol Busters, or Angina-B-Gone.

Why is drug classification and nomenclature so important in pharmacology?

They provide a clear and unique identifier for active chemical substances, appearing on all drug labels, advertising, and other information about the substance.

In what way is a generic drug different from a brand name drug?

The difference between brand name and generic drugs is in the circumstances of producing the drugs. While brand name drug refers to the name giving by the producing company, generic drug refers to a drug produced after the active ingredient of the brand name drug.

What is branded medicine?

Brand name medicine is originally discovered and developed by a pharmaceutical company. Brand name medicine is approved by FDA by submitting a New Drug Application along with data regarding proof of characteristics of dosage form, manufacturing, chemistry, stability, efficacy, safety, labeling and packaging.

Why are branded drugs more expensive?

Brand Name Drugs This ends when the registered patent expires. Only then can other medicine manufacturers file to create a generic version, with only a 3.5\% difference in absorption from the brand name drug. This is also the reason why brand name drugs are usually more expensive than generic versions.

How do pharmaceutical drugs get their names?

Pharmaceutical names are assigned according to a scheme in which specific syllables in the drug name (called stems) convey information about the chemical structure, action, or indication of the drug.

Why are pharmaceutical names so weird?

There’s a reason so many drug names look so weird. A good drug name is supposed to check lots of boxes. It should be easy for doctors to spell accurately when they scribble it down on a prescription pad. It should be memorable.

Why do drugs need to be classified?

Classifying drugs by chemical similarities is useful because drugs that are chemically similar often have similar impacts and risks. An individual who is addicted to a given drug is more likely to abuse a chemically similar drug.

Why is it important to know the classification of drugs?

Drug classifications are important. They help protect you from severe side effects and drug interactions. They help ensure your body can break down and use the medication. They help guide many treatment decisions.

What are the advantages and disadvantages of a generic versus a brand name pharmaceutical product?

Cheaper prices. The main reason so many people buy generic drugs is because they are so much cheaper than brand name drugs. Brand name drugs require research and testing that take a lot of time and money, but generic drugs only need to copy what already exists, saving them the cost and allowing the price to stay low.

Why is it best to study drugs by their generic names rather than by their brand name?

Generic and brand names must be unique to prevent one drug from being mistaken for another when drugs are prescribed and prescriptions are dispensed. To prevent this possible confusion, the FDA must agree to every proposed brand name.

What happens when a tablet comes out of a tablet machine?

III. Tablet Deduster: In almost all cases, tablets coming out of a tablet machine bear excess powder on its surface and are run through the tablet deduster to remove that excess powder. IV.

Is tablet technology changing the way medicines are made?

Although the basic medicinal approach for their manufacture has remained the same, tablet technology has undergone great improvement.

What is the cause of capping of tablets?

CAPPING: – It occurs when the upper or lower part of the tablet separates horizontally (partially or complete) from the tablet body and comes off as a cap, during ejection of tablet from the compression machine. Causes – over drying of granules, lesser amount of binder, improper tooling, air entrapment.

How many tablets are used to collect data across three countries?

A total of 32 data collectors used 49 electronic tablets to collect data across three countries (India: 5, Pakistan: 19, and Kenya: 25). All data collectors were trained healthcare providers (nurses, midwives, doctors), working in the study healthcare facilities, with varying levels of experience of using electronic devices.