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Medication errors in the medical field
Medication error risks
Medication errors in the medical field
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A situation in which a pharmacy might be held liable for negligence is when a pharmacist knowingly dispenses a drug that is inferior or defective or when the physician has substituted a generic drug when the physician has prohibited the action in an expressive manner. Also, the pharmacist might have asked the patient to authorize the substitution may inadvertently create an express warranty that the prescribed drug is "as good as" or "the same as" the one prescribed. This is something that happened in Jacobs Pharmacy Co. v Gibson. In this case, the plaintiff presented a prescription for Zephiran Chloride Aqueous Solution 1:750 to a pharmacy technician. The technician informed the plaintiff she did not need the prescription since there was an over-the-counter (OTC) product that was the "same as" the prescription product. …show more content…
The court found that when a pharmacy technician represents that a packaged product is "the same as what the plaintiff's prescription called for," liability will be found if the substituted product causes injury. For instance, a patient could have come to take Paracetamol for her 2 month old baby having fever but because of it being out of stock, the pharmacist replaces it with Calpol. But Calpol is not meant to be used for kids under 3 months of age. In this case a pharmacist would be held liable for injuries caused by the substituted drug. The kid could be allergic to a particular chemical in the Calpol. Also, the pharmacy would be held liable if it failed to warn the patient that the prescription drug was contra-indicated for people, like the patient, who was allergic to a particular compound. But this must mean that pharmacy had the actual knowledge of the allergy and a system in place to alert the pharmacist to that
The two of the six rights of medication administration that were violated where the right medication, the right dosage, and the right client. The nurse failed to read the medication order three times before administering the medication, failed to scan for the right count of the medication, and as well failed to match the patient ID with the scanned
contamination, toxicity, and side effects. Most people believe these medications are compounded or mixed by a trained and licensed individual. However, this is inaccurate because the pharmacy technician actually compounds a large percentage of a patient’s medications. Compounding involves a techn...
Giving out the wrong medication, or improper dosages can potentially be fatal to patients. Pharmacy technicians must be willing to take on this risk and do their work as carefully and accurately as possible.
The main quality initiative affected by this workaround is patient safety. The hospital switched to computer medication administration as opposed to paper medication administration documentation because it is supposed to be safer. So, when the nurse gets the “wrong medication” message the computer thinks something is wrong, this is a safety net that is built into the computer system. If the nurse were just to administer the medication without any further checks, he or she would be putting patient safety on the line. The policy involved that pertains to this workaround is the “8 rights of medication administration”, which are: right patient, right medication, right dose, right route, right time, right documentation, right reason, and right response (LippincottNursingCenter®, 2011). Each nurse it taught these eight rights of medication administration in nursing school, therefore it is a nursing policy. When this workaround occurs the nurse should use his/her judgment before “scan overriding” and ensure these eight checks before administering the
US’s pharmacists have their hands tied and are demanding every patient to receive the precise medication prescription they have written up for. On the other hand, being a pharmacist is more than that, it is about building your patients’ knowledge on the risks and potential hazards on certain medications they are prescribed to. With that being said, this means that a pharmacist’s job is directly providing for patient in order to help them live a long healthy life within their scope of practice. Pharmacists cannot afford for any errors to occur and taking the time to make sure the accurate bottle of medication falls into the right patient’s hands is a huge responsibility for pharmacists
The following paper discusses the Federal False Claims Act, 31 U.S.C. §§ 3729-33 in more detail. While such violations may involve various types of health care providers, focus is placed on the applicability of the law within the pharmaceutical sector of health care. The roles and responsibilities of a health care administrator within the pharmaceutical sector are also discussed considering the impact this entity may play in preventing such violations (e.g., knowledge of law, how it impacts daily operations, consulting with legal entities, regulatory compliance, etc.).
All in all, administering medications takes a great deal of responsibility and care to prevent errors from occurring. It is also important to know that administering medications to the elderly can be significantly different because of their physiological changes. Finally, it is important to have a system like the six rights and three checks to consonantly screen against medication errors.
There are many reasons that we must make sure that the brand is the same. The number one reason is due to the fact that a change in brands can have an effect on the patient’s levels during testing. The next biggest reason is due to the fact that the change in brands also comes with change in color, shape, and sometimes size this causes confusion for the patient’s. So when filling a prescription if at possible we as technicians try our hardest to make sure that we use the same brand that the patient received on their last
5. The pharmacist or pharmacy technician will then fill the prescription from the pharmacy's inventory as ordered by the doctor. Generics may be substituted where allowed by law or the
Pharmacy is a booming field when it comes to medicine, but it certainly has controversial issues such as compounding drugs. While the practice of making drugs customized to a patient seems ethical, there are problems that come along with it. Drug compounding was the norm in the past, but over time consumers began to see issues with it. Drug compounding still occurs to this day because some patients do need medicine specifically tailored to their needs. Compounding has also been the focus of recent disasters, some of which occurred less than two years ago. Whatever side one may take on this issue, it is clear that compounding medicine will be a polarizing issue for years to come.
As the third paragraph states, the medicines should only be used to a patient's consent, it should also be used only to an extent. If a patient has chosen to take the odd side of the medicinal route, the strange medicines should only be used until the patient is healthy enough to be placed on a more desireable treatment. If a different medicine could be used, then the physician should not use this, to the patient's wills of course.
Inside most packaging all prescription medication from a pharmacy are instructions and disclaimers for the product; these instructions includes a list of prescriptions that conflict with the medication, side effects of the drug itself, allergic reactions, phone numbers to call if the drugs affect you badly, emergency methods to prevent death and information on the statistics included in the drug testing and chemical analysis. Unfortunately many people never read ...
The goal of any medication practice and dispension is to improve the quality of life of the patients while minimizing the medication risk to the patient. Patients are always subject to errors and risk during the medication period. Medication errors include among others prescription errors, dispensing errors, medication administration errors, omission of ordered drugs, timing, and even patient compliance errors (Goldspiel et al., 2015). Health care organizations are centers for care and rescue for patients suffering from different health issues. Therefore, it is the duty of the health care managers and providers to ensure that patients do not develop further health issues and complication due to the medical errors.
Dispensing errors can be defined as content errors and/or labeling errors1. These errors generally involve pharmacists dispensing the wrong product to the patient or displaying wrong information on the dispensing label1. Error of medicinal content could mean supplying patient with a different product, strength, form or quantity from the prescription. Displaying the wrong information on the dispensing label could mean different patient’s name, different description of the medication or different dose. These errors can happen at any stage of the dispensing process. However, it is the duty of pharmacists to intercept these errors before it reaches the patient that potentially cause harm or even death. In this essay, I will discuss whether it is fair for pharmacists to face legal action for dispensing errors.
Adverse drug events are a leading cause of mortality in the United States. 82% of American adults take at least one medication and 29% take five or more medications. Prevention of risk associated with of medication is to improving quality of health, maintaining life, and decreasing he cost of associated medical expenses. There are many entities within the healthcare environment, (government, providers, non-profit and oversight committees) working to reduce medication errors. One such government entity is the Patient Safety Organization and the