Why You Should Pay Attention To Drug Recalls

Don’t Ignore Drug Recalls!

If you regularly take prescription drugs, you need to be paying close attention to drug recalls. If there is an issue with a medication you are taking, you may not be notified right away. The sooner you find out about this recall, the better. If a medication you take is recalled, you’ll want to discuss it with your doctor right away.

Drug Recalls Aren’t Taken Lightly

Once a prescription drug has been approved by the FDA, it isn’t easy to recall that drug. Since so many people rely on the medications that they take, recalls tend to be rare. A drug isn’t going to be recalled because of a minor problem. If a recall is happening, it is for a serious reason.

If a medication you take has been recalled, you may be at risk for serious illness or side effects. That’s why you need to find out about the recall as soon as you can. If you learn about the recall right away, you can take steps to keep your body healthy.

Prescriptions Can Last For A Long Time

A lot of people assume that they can ignore drug recalls. After all, if one of the medications they take is recalled, they should be notified at their next doctor’s visit. However, a lot of people forget just how long a prescription can last.

If you don’t find this information on your own, it could be weeks or even months before you learn that the medication is recalled. You could cause a lot of damage to your body during that time. You’ll have a better chance if you learn about the recall right away.

You’ll Want A Doctor To Examine You

If you have been taking a medication that is potentially harmful, you’re going to want to have a doctor take a look at you. Your doctor should examine you and see if they notice any problems.

If a medication has harmed you, you will want to treat that sooner rather than later. If you ask your doctor to examine you, they will be able to identify any problems that exist. From there, they will be able to recommend the best available treatment.

drug recalls

When You Pay Attention To Recalls, You Don’t Have To Quit Your Meds Cold Turkey

Simply dropping a medication you take daily can be harmful. You may experience withdrawal symptoms, and other health issues could arise as well. If you’re going to be dropping a medication, you are going to want to do so under the guidance of your doctor.

If you’re not paying a lot of attention to drug recalls, you may be caught off guard. This could lead you to make poor decisions. If you are following the news and learn about a drug recall right away, you’ll have a lot more options.

It’s important for anyone that takes regular medication to pay attention to drug recalls. Recalls aren’t something that you can afford to ignore. The more you know about what is going on with medication, the better.

What Is the History of Drug Recalls in the United States

Drug Regulation and Recalls

Though the pharmaceutical industry is an integral part of the country today, that has not always been the case. Although medical professionals and various types of cures existed in the early years of the United States, the drugs used for treatment were not processed in huge sterile factories like they are today.

The history of drug production in the country has a checkered past. In addition to the prescription drugs meted out by doctors and other medical professionals, over-the-counter medications are huge business. In both areas of drug production, there have been mistakes leading to recalls of the products. In some cases, the companies even sent out the bottles knowing that the product was inferior in some way because it was cheaper than throwing the contaminated batch away.

The history of drug recalls extends back to when the US started regulating industries. Prior to the Industrial Revolution, there was no need for this kind of oversight. However, as more and more men were drawn away from their homes and into industrial production jobs, that began to change. Over time a wide range of rules has been established in order to keep workers safer and to help ensure that the products ending up in consumer’s hands are accurately labeled and safe.

drug regulation

The severity of the consequences for breaking these rules can vary from mild to fatal. In regards to the drug industry, this could mean stomach cramps for a few hours or death by poison. As such, the industry is expected to respond quickly to ensure that consumers are informed and products recalled that have been deemed unsafe.

Though this is an excellent idea many people today have trouble keeping up with the recalls that happen virtually every day. Some big box retailers have a place where you can view the products they carried that have been recalled. However, a much better alternative is to visit the government website that lists all of the products that are on recall lists.

By doing this on a regular basis, you can find out if anything specifically related to your household has been placed on the list. Remember that even over-the-counter drugs are subject to recall.

One of the most well-known recalls in the history of the United States relates to the Tylenol scare in the early 1980’s. Several people died in the incident that inspired drug manufacturers to start sealing the bottles for greater protection. Other industries followed suit in an effort to avoid their products being contaminated by a rouge.

More recently a drug for children was recalled after it was discovered to contain the incorrect amount of the active ingredient. Between these incidents have been many other cases where people became ill as a result of ingesting a product that they believed to be safe. No matter how much regulation and oversight involved in production there will inevitably further recalls in the future for pharmaceuticals at the store and from your doctor.

International Drug Companies Must Comply With US Law

Drugs, Regulation, and Crossing Borders

Have you ever wondered if International Drug Companies fall under the same regulations as US-based drug manufacturing companies do when selling those products inside the US border? For anyone who lives in the US and depends on the drugs that are available here, it is an important question. While there are some controversies over the FDA and how it approves new drugs, the average American does want to know that both over-the-counter and prescription drugs do meet FDA approval.

How Does The FDA Regulate Foreign And International Based Drug Companies?

Where a drug is made has no bearing on if that drug can be sold within US borders. Anytime a company wants to sell over-the-counter and prescription based drugs in the US they must go through the approval process set forth by the Federal Food and Drug Administration. The FDA sets forth a number of stringent rules that the manufacturers of drugs must meet to guarantee its quality as well as the product label requirements.

In order for a company to be approved for the production and sale of drugs in America, they must allow the FDA to give regular inspections of the manufacturing process and of course all ingredients to make sure that they meet all applicable laws and are in complete compliance with them. The Food and Drug Administration will test drugs that are sold in retail stores and manufacturing sites as well as distribution centers. If a complaint comes in from a consumer or from health care professionals about any concerns, then the FDA and will investigate the matter.

drug companies

Foreign-Made Drugs Are Rapidly Increasing In The United States

A very large amount of the drugs being sold inside the US are either fully and completely manufactured overseas or are manufactured here in the US but the process uses foreign-made ingredients in the drugs. In the last several years the amount of foreign made drugs and drugs with foreign ingredients has more than doubled and the estimates are that it is going to continue to increase in coming years. According to the FDA, its globalization initiative is designed to meet the difficult challenges of testing and processing imported drugs and products that are used in the drugs to ensure that they meet American Standards.

The FDA is working with foreign government agencies in the effort toward improving the relationships there and to better ensure that the FDA is able to inspect foreign-based drug companies and the products and drugs that are being produced there. As anyone would expect, it’s a complex and complicated matter and it’s one that is likely to always demand the utmost care. The FDA is hoping that this initiative will not only help them but also the government agencies they work with as these agencies all work together in reporting any drug situations that are found to be unsafe.

Obviously, the FDA is an organization that regulates the legal sale of drugs to Americans. For that reason, they do not regulate any type of illegal manufacturing of drugs. The sale of illegally manufactured drugs that are imported into America through the Canadian border or that are sold online are some of the drugs that do make their way into the US without being approved by the FDA.