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Drug expiration is the date after which a
drug A drug is any chemical substance that causes a change in an organism's physiology or psychology when consumed. Drugs are typically distinguished from food and substances that provide nutritional support. Consumption of drugs can be via insuffla ...
might not be suitable for use as manufactured. Consumers can determine the
shelf life Shelf life is the length of time that a commodity may be stored without becoming unfit for use, consumption, or sale. In other words, it might refer to whether a commodity should no longer be on a pantry shelf (unfit for use), or no longer on a ...
for a drug by checking its
pharmaceutical packaging Pharmaceutical packaging (or drug packaging) is the packages and the packaging processes for pharmaceutical preparations. It involves all of the operations from production through drug distribution channels to the end consumer. Pharmaceutica ...
for an expiration date. Drugs which are past their shelf life can
decompose Decomposition or rot is the process by which dead organic substances are broken down into simpler organic or inorganic matter such as carbon dioxide, water, simple sugars and mineral salts. The process is a part of the nutrient cycle and is ...
and either be ineffective or even harmful. Standard advice from drug manufacturers and some health organizations is to dispose of drugs after the expiration date printed on the packaging. However, the published expiration date is not an absolute indication that a drug has spoiled. Consumers and organizations sometimes use expired drugs for medical treatment either as a cost saving measure or because they otherwise cannot access drugs which are not expired. Medical authorities find it difficult to discuss when consumers can safely use drugs after the printed expiration date because it is difficult to obtain clear information.


Labeled expiration date versus true expiration

Manufacturers print expiration dates on drug bottle labels. The labeled expiration date is a manufacturer's promise for a time until which the drug will have full efficacy and be safe as manufactured. The labeled expiration date is not an indication of when a drug has become ineffective or unsafe to use. Many drugs are effective for years after their expiration dates. However, it is difficult for anyone including researchers and physicians to find information to verify how much any given drug will degrade in efficacy or become unsafe over time. Drug manufacturers never support the use of drugs after the expiration date because that could make them liable if something went wrong. The expiration date printed on drug packaging will differ from the true expiration date of the drug. Before the true expiration of a drug, its
active ingredient An active ingredient is any ingredient that provides biologically active or other direct effect in the diagnosis, cure, mitigation, treatment, or prevention of disease or to affect the structure or any function of the body of humans or animals. T ...
will retain its potency. Also before expiration, no components of the drug will degrade to become harmful. Since products continually change over time, the characteristics of any drug are not unchanging but instead estimated with
assay An assay is an investigative (analytic) procedure in laboratory medicine, mining, pharmacology, environmental biology and molecular biology for qualitatively assessing or quantitatively measuring the presence, amount, or functional activity of a ...
measurements to be within the
specification A specification often refers to a set of documented requirements to be satisfied by a material, design, product, or service. A specification is often a type of technical standard. There are different types of technical or engineering specificati ...
required by the government regulator where the drug is sold. As a general estimate, a drug becomes unfit for use when 10% of the active ingredient is degraded. Before choosing an expiration date to print the manufacturer must first decide a true expiration date. After a manufacturer has decided what true expiration date it has set, then it will decide another date to make public and advertise on the packaging of the drug. The printed expiration date will always be sooner than the true expiration date, because the drug should always be effective and safe before the labeled expiration date if kept properly.


Options for expired drugs


Disposal

The United States'
Center for Drug Evaluation and Research The Center for Drug Evaluation and Research (CDER, pronounced "see'-der") is a division of the U.S. Food and Drug Administration (FDA) that monitors most drugs as defined in the Food, Drug, and Cosmetic Act. Some biological products are also leg ...
officially recommends that drugs past their expiration date be disposed. It has been argued that this practice is wasteful, since consumers and medical facilities are encouraged to purchase fresh medication to replace their expired products, also resulting in additional profits for pharmaceutical firms.


Consumer use as normal

Some consumers can face the difficult position of being unable to afford their medication, and choosing between using expired medication or forgoing medication. An
epipen An epinephrine autoinjector (or adrenaline autoinjector, also known by the trademark EpiPen) is a medical device for injecting a measured dose or doses of epinephrine (adrenaline) by means of autoinjector technology. It is most often used for t ...
is an example of an expensive medication which someone might consider using after expiration because of inability to purchase newer medication. Some common drugs which authorities say are always unsafe if expired include
nitroglycerin Nitroglycerin (NG), (alternative spelling of nitroglycerine) also known as trinitroglycerin (TNG), nitro, glyceryl trinitrate (GTN), or 1,2,3-trinitroxypropane, is a dense, colorless, oily, explosive liquid most commonly produced by nitrating g ...
,
insulin Insulin (, from Latin ''insula'', 'island') is a peptide hormone produced by beta cells of the pancreatic islets encoded in humans by the ''INS'' gene. It is considered to be the main anabolic hormone of the body. It regulates the metabolism o ...
, and liquid antibiotics. Consumers sometimes store drugs which they ought not use, regardless of being expired. People who have leftover antibiotics might feel that they can use them safely if they are not expired, or even if they are expired. Medical authorities recommend that no one use prescription drugs except under a physician's care. Authorities also encourage care in storing
over-the-counter drugs Over-the-counter (OTC) drugs are medicines sold directly to a consumer without a requirement for a prescription from a healthcare professional, as opposed to prescription drugs, which may be supplied only to consumers possessing a valid prescr ...
, discarding them on a regular schedule, and using them as directed when appropriate.


Drug recycling

Drug recycling is a fringe and experimental concept but in some places it happens. Sometimes, an individual or organization will have valuable medicine which they do not intend to use. If that medication could be used by other people before its expiration, then sometimes, interested parties discuss
drug recycling Drug recycling, also referred to as medication redispensing or medication re-use, is the idea that health care organizations or patients with unused drugs can transfer them in a safe and appropriate way to another patient in need. The purpose of su ...
to transfer ownership of the drugs away from the party which will not use them to the party which needs them. In such discussions, anyone considering the transfer of drugs will also consider if drugs could be used before their expiration.


Shelf Life Extension Program

To reduce the cost to the military of maintaining stockpiles of certain pharmaceuticals, the
United States Department of Defense The United States Department of Defense (DoD, USDOD or DOD) is an executive branch department of the federal government charged with coordinating and supervising all agencies and functions of the government directly related to national secu ...
and the
Food and Drug Administration The United States Food and Drug Administration (FDA or US FDA) is a List of United States federal agencies, federal agency of the United States Department of Health and Human Services, Department of Health and Human Services. The FDA is respon ...
operate a joint initiative known as the Shelf Life Protection Program (SLEP), which evaluates the long-term effectiveness of medications stockpiled by the DoD and other government agencies. Under the program, medications are tested for safety and stability for extended periods of time in controlled storage conditions. In many cases, medications tested were found to be effective for years past their printed expiry dates; a 2006 study by the
Journal of Pharmaceutical Sciences The ''Journal of Pharmaceutical Sciences'' is a monthly peer-reviewed scientific journal published by Elsevier on behalf of the American Pharmacists Association, with the support of the International Pharmaceutical Federation. It is also publishe ...
found that two-thirds of 122 medications tested through SLEP remained effective for an average of at least four additional years. In 2016, the DoD reported that the program had helped save the department $2.1 billion on replacing stockpiled medications.


References

{{reflist, 3 Product expiration Drug safety