MedWatch receives safety alerts for FDA-regulated products

MedWatch There is some scary new news.  A new report has been released that is truly alarming.  The report issued by the Institute of Medicine (IOM) found that adverse drug events are at crisis level.  It has been estimated that an estimated 1.5 million people each year are effected. An estimated cost of approximately $3.45 billion US dollars . Furthermore, these statistics do not take into account lost wages and loss in productivity.  Furthermore, they don’t factor in the added health care costs that happen because of these injuries.

The National Academies are very worried about these documented health implications.  In fact, the IOM’s findings ought to force government agencies and health care professions to adress the crisis.  Even communities need to work together to improve patient safty.  This can be done by creating new and improved drug information resources,.  Finally, trying to make complicated drug naming and labeling much simpler.

PURPOSE of MedWatch

MedWatch has two mission statements.  First of all, it supplies AERS tools that allow medical professionals and the public to report medication errors .  The same applies to any kind of medical product injuries. MedWatch also provides clinical information.  For example info on  prescription medications, OTC pills and supplements, biologics, medical and radiation-emitting devices.  The list also included any kind of special nutritional products or supplement, and dietary supplements.

 

DESCRIPTION

MedWatch focuses on drug and medical device reporting. It offers a choice between a voluntary reporting form, designed primarily for health care professionals and the general public, and a mandatory AERS reporting form, available to manufacturers, importers, and medical product user facilities that manage and store medical products. The latter group is required by law to submit the mandatory form immediately upon discovery of a product malfunction. Printable mail-in forms are available as an alternative to the online submission.

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  MedWatch is a reporting entity that receives reports from the public.  When needed, MedWatch publishes safety alerts for the FDA.  MedWatch will rate products such as:

  • A series of Combination products.  For example,  pre-filled drug syringe, monitored kinds of-dose inhalers and certain kinds of prescription nasal spray.
  • Specialized nutritional foods and supplement  these are made of kinds of dietary supplements and medical foods.  This also includes infant formulas.
  • All Prescribed Medications as well as OTC pills(over-the-counter pills)
  • Cosmetics .  This group will include shampoos, soaps, moisturizers and  makeup.  Also included are hair dyes and even body tattoos.
  • Biologics such as blood components, blood/plasma derivatives.  Biologics will also include modern gene therapies.
  • Medical devices such as, pill dispensers, hearing aids and pacemakers.
  • Special nutritional products such as dietary supplements, medical foods and infant formulas.
  • Ingestible like ingredients added to foods and proteins and vitamin drinks.

MedWatch receives safety alertsThere are many other products that the FDA monitors and regulates.  To illustrate, cigarettes’, cigars, chewing tobaccos.  Also included,  vaccines,  animal drug, medication dispensing devices and even pet t food. All of these different product lines use different kinds of reporting methods.  The reports concerning these products ought to be turned in to the correct reporting portals.  

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medication mistakes

October 16, 2023 No Comments

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