File Name: list of generic and brand name drugs .zip
Generic Drugs. Some patients have the misperception that generic drugs are inferior to brand name drugs. Bioequivalent drug formulations have the same bioavailability; that is, the same rate and extent of absorption. New drug formulations must meet standards set by Health Canada. If the generic drug is bioequivalent, it is assumed that it will produce the same therapeutic effect as the brand name drug.
If you want to use a drug list to find out if we cover your medication, this information will help you understand how to read one. You can use drug lists to see if your health plan covers your prescription medication. Most of the medications on our drug lists are grouped by tiers so that you can find out if your health plan covers your prescription. The least expensive drugs are in the lower tiers. Not every insurance plan has the same drug list, but there are a few things you should look for no matter which drug list applies to your plan.
Despite this variation in cost, barriers such as lack of communication and education, previous side effects, or preference may play a role in continued use of brand-name medications. Having an increased generic product market will create competition and, ultimately, lead to lower drug prices and access to affordable healthcare for more patients. It is important that pharmacists educate patients and providers on the appropriate use of generic versus brand medications. Abbreviated New Drug Applications ANDAs for generic approvals must show bioequivalence and that the active ingredient is the same as the brand name; they may differ based on the inactive ingredients, but these differences must be proven to have no effect on how the medication works. The Drug Price Competition and Patent Term Restoration Act, or Hatch-Waxman Act, allowed for generics to be approved for market use without preclinical and clinical testing to ensure a generic would be lower in cost compared with its equivalent branded product.
The resources below have been provided to help narrow your search to specific, targeted drug information. Information is available for both consumers and healthcare professionals on over 24, prescription and over the counter medicines available primarily in the USA. Multum leaflets provide basic consumer drug information, such as drug descriptions and interactions, details of possible side effects and the effects of missed doses and overdosing, as well as instructions for use. The leaflets are available in English and Spanish. IBM Watson Micromedex Advanced Consumer Information provides comprehensive consumer information pertaining to a wide variety of drugs, such as a list of commonly used brand names, drug descriptions, warnings and precautions, and detailed information on the proper use of each drug. A wholly independent staff of drug information pharmacists and other professional editorial and analytical staff thoroughly research AHFS DI content. Authors incorporate clinical research findings, therapeutic guidelines, and Food and Drug Administration FDA approved labeling to ensure that monographs include an evidence-based foundation for safe and effective drug therapy.
Drug nomenclature is the systematic naming of drugs , especially pharmaceutical drugs. In the majority of circumstances, drugs have 3 types of names: chemical names , the most important of which is the IUPAC name ; generic or nonproprietary names , the most important of which are the International Nonproprietary Names INNs ; and trade names, which are brand names. Drug names are often subject to legal regulation, including approval for new drugs to avoid confusion with existing drugs and on packaging to establish clear rules about adulterants and fraudulent or misleading labeling. A national formulary  is often designated to define drug names and purity standards for regulatory purposes. The legally approved names in various countries include:.
A generic drug is a medication created to be the same as an existing approved brand-name drug in dosage form, safety, strength, route of administration, quality, and performance characteristics. A generic medicine works in the same way and provides the same clinical benefit as its brand-name version. This standard applies to all FDA-approved generic medicines. A generic medicine is the same as a brand-name medicine in dosage, safety, effectiveness, strength, stability, and quality, as well as in the way it is taken and should be used. Generic medicines use the same active ingredients as brand-name medicines and work the same way, so they have the same risks and benefits as the brand-name medicines.
Hover over each icon below for an explanation of their meaning. Scroll down to find all drugs and dosages that can offer savings or information by clicking on the drug name then click on the icon. If doing a drug search, scroll down to see your drug search results. Programs created by pharmaceutical companies to provide free or discounted medicines to people who are unable to afford them.
Understanding the differences between generic and brand name medications can help injured workers understand their workers' compensation prescriptions a bit better. When you experience an on-the-job accident or illness, you have to become fluent in medical jargon pretty quickly. It's helpful to know the ins and outs of the medications that your doctor prescribes. Getting to know generic medications versus brand names is the first step. According to the FDA, nearly 8 in 10 prescriptions filled in the United States are for generic drugs.
A generic drug is a pharmaceutical drug that contains the same chemical substance as a drug that was originally protected by chemical patents. Generic drugs are allowed for sale after the patents on the original drugs expire. Because the active chemical substance is the same, the medica l profile of generics is believed to be equivalent in performance. Although they may not be associated with a particular company, generic drugs are usually subject to government regulations in the countries in which they are dispensed.
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