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Category: Medication Errors

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Medication errors happen more often than most people realize, and the consequences can range from a minor setback to something genuinely life-altering. If you or someone you care about was harmed by the wrong drug, a wrong dose, or a missed interaction, one of the first questions you’re probably asking is: who is actually responsible for this?

That question matters a lot in Rhode Island, and the answer is rarely simple. Our team handles these cases regularly, and we want to walk you through how liability actually works when a medication error medical malpractice claim is involved. Understanding who can be held accountable is the first step toward knowing whether you have a case worth pursuing.

The Medication Process Involves More People Than You Think

Think about what happens between a doctor deciding you need a medication and that medication actually entering your body. There’s a physician writing the prescription. A nurse or medical assistant may transcribe it. A pharmacist fills it. A nurse or home care aide may administer it. Any one of those steps is a potential point of failure.

A medication error is broadly defined as a preventable event that may cause or lead to inappropriate medication use or patient harm. It can happen at any stage of the medication process, including prescribing, transcribing, dispensing, administering, or monitoring. That’s a long chain of hands, and liability can attach at any point along it.

Doctors and Prescribing Providers

Physicians carry a significant duty when it comes to medication. Physicians, pharmacists, and anesthesiologists have a duty to prescribe, dispense, or administer medications safely. Negligence may occur when they fail to check patient medical history, prescribe an incorrect dosage, or neglect to inform patients of potential side effects.

Drug interactions are another common source of liability. If any of the healthcare providers in the whole medication chain misses or transposes a decimal point, the patient could be administered ten times too much or too little medication. 

Pharmacists and Pharmacies

Pharmacists are not just order-fillers. They carry an independent professional duty. Pharmacists can be held liable for medication errors if they dispense the wrong medication or dosage, mislabel the medication, or fail to provide proper counseling to the patient about how to take the medication safely.

And here’s something people often don’t realize: the pharmacy itself, not just the individual pharmacist, may also be on the hook. In Rhode Island, you may be able to hold both an individual pharmacist and the company they work for accountable for injuries sustained due to incorrect dosage or medication, poor or missing instructions, and other examples of pharmacist negligence. 

Hospitals and Healthcare Facilities

Hospitals occupy a unique and sometimes complicated position in medication error cases. If the medication error occurs within a hospital or healthcare facility, the institution may bear liability for inadequate systems or protocols in place to prevent errors, insufficient staffing levels, or failure to properly train staff.

That said, Rhode Island has a wrinkle worth understanding. In Rhode Island, many healthcare professionals are independent contractors rather than employees of the hospitals where they work. This means that even if the injury occurred in a hospital, the hospital may not automatically be liable. However, exceptions exist, especially in cases involving emergency departments, inadequate supervision, or negligent credentialing.

Drug Manufacturers

Sometimes the medication itself is the problem. In many cases, a pharmaceutical manufacturer may be accountable where a drug caused a patient injury and the maker failed to caution people of prospective negative effects or dangers of the drug. This moves the case into product liability territory rather than traditional medical malpractice, but the underlying harm to the patient is no less real.

Unclear labeling, dangerous packaging similarities between two different drugs, or inadequate warnings about known interactions can all potentially implicate a manufacturer. These cases tend to be more complex and often involve federal regulatory frameworks alongside Rhode Island state law, but they are absolutely worth evaluating.

Multiple Parties Can Share Liability

This is where medication error cases get genuinely interesting from a legal standpoint. In some cases, multiple parties may share liability. For example, both a doctor and the facility may be responsible if systemic failures contributed to the harm.

Imagine a patient admitted to Rhode Island Hospital for a routine procedure. The admitting physician orders a medication. The order gets transcribed incorrectly. The pharmacist fills the incorrect order without flagging the discrepancy. The nurse administers it without double-checking against the patient’s chart. The patient is harmed. Who is responsible? Potentially all of them, to varying degrees.

Identifying all of the potentially liable parties is one of the most important things an attorney does early in a medication error case. 

What You Need to Prove

Under Rhode Island law, to prove liability for a medication error, you must first establish the standard of care imposed on the medical provider. From there, you need to show that the provider deviated from that standard, and that the deviation caused your injury. That sounds straightforward, but in practice it requires medical testimony, careful review of records, and often a detailed reconstruction of what happened and when.

Medical malpractice law in Rhode Island holds healthcare providers legally accountable when they fail to meet the accepted standard of medical care, resulting in patient injury, illness, or death. This area of law recognizes that while most medical professionals provide exemplary care, patients deserve legal recourse when negligent treatment causes preventable harm.

The Filing Deadline in Rhode Island

In Rhode Island, any medical malpractice claim arising out of a medication error must be pursued within three years of the occurrence of the incident that gave rise to the action. Miss that window and your options become limited.

There is a discovery rule that can extend this deadline in certain circumstances. The discovery rule is an exception to the standard deadline in situations where injured patients could not reasonably have learned that they had a medical malpractice case. In Rhode Island, the discovery rule states that a medical malpractice plaintiff has three years from the date that the alleged malpractice should, in the exercise of reasonable diligence, have been discovered.

And there are some specific exceptions. If the victim of medical malpractice was under disability by reason of age, their case may be brought at any time up to age 21. Rhode Island also may affect the limitations period if a defendant fraudulently conceals the cause of action by actual misrepresentation, is absent from the state without attachable property, or if the victim is mentally incompetent.

But relying on an exception is a legal risk. We always advise clients to act as quickly as possible rather than bank on an exception applying to their situation.

What to Do If You Think a Medication Error Harmed You

Reach out to an attorney as soon as possible. The process of building a medication error case takes time: gathering records, identifying the right defendants, retaining medical reviewers, and understanding exactly where the chain of care broke down. Starting early gives your case the best possible foundation.

At DeLuca, Weizenbaum, Barry & Revens, Ltd., we work with clients across Providence County and throughout Rhode Island who have been harmed by medication errors. Contact us to talk through your situation.

Prescription medications are supposed to help. That sounds obvious, but it is worth saying plainly because what happens when a doctor prescribes something and then never checks in again is anything but obvious to most patients. In our experience at DeLuca, Weizenbaum, Barry & Revens, Ltd., patients across Providence, Cranston, Warwick, and communities throughout Rhode Island often discover too late that a physician’s failure to track how a medication is affecting them can cross the line from a bad outcome into something the law recognizes as medical negligence.

So when does that line actually get crossed? That is the question we want to address here, because the answer matters a great deal to anyone who has suffered serious harm from a medication they trusted their doctor to manage.

What Doctors Are Actually Supposed to Do

Prescribing a medication is not the end of a physician’s job. It is often the beginning of an ongoing obligation. Clinicians are generally expected to maintain an updated list of all current medications prescribed for a patient, including those prescribed by other physicians. Beyond that, certain medications require active follow-up. Blood tests, symptom check-ins, dosage adjustments. The level of monitoring depends on what is being prescribed and what the patient’s overall health picture looks like.

Consider a patient at Rhode Island Hospital or The Miriam Hospital who is put on a medication known to carry risks of organ stress. Standard practice calls for periodic lab work to catch problems early. If a physician prescribes that medication and then never orders a follow-up test, never asks about symptoms, and never updates the chart to reflect what the patient is actually experiencing, that gap in care can be significant. Improper monitoring of medication may prevent a patient from getting the full benefits of their medication or open them up to possible overdose, harmful side effects, harmful interactions with other medications, or exacerbations of other medical issues.

And another thing worth knowing: the duty to monitor does not rest only on the prescribing doctor. Nurses are responsible for administering medication and monitoring patients in inpatient healthcare settings and can be held liable if they make mistakes. Pharmacists carry obligations around flagging dangerous interactions. Hospitals themselves can face liability when their staffing or systems create the conditions for these failures. The chain of responsibility in a medication side effect case can involve several parties.

What Rhode Island Law Requires You to Prove

Rhode Island law does not hand anyone a malpractice claim simply because a medication caused harm. The legal standard is more specific than that, and it is worth understanding before drawing conclusions about your situation.

Rhode Island courts have held that a plaintiff must establish the degree of diligence, knowledge, or skill that a healthcare provider practicing in the same field or specialty would ordinarily have and exercise, that the provider either lacked that skill or failed to exercise the appropriate level of care, and that the patient sustained injuries that would not have occurred except for the provider’s negligence.

More precisely, this breaks down into four practical questions. Did a treatment relationship exist between you and the provider? Did that provider fail to meet the accepted standard of care? Did that failure directly cause your injury? And did you suffer real, documentable harm as a result? Missing any one of those elements can sink an otherwise compelling case.

The standard of care question is where medication monitoring cases often turn. The Rhode Island Supreme Court clarified that the standard of care depends on what a similarly qualified physician or provider would have done, not simply what others in the local community do. That is meaningful because it holds Rhode Island physicians to a national benchmark, not just what the doctor down the street might have done.

What Makes a Case Strong Versus Weak

Strong cases in this area tend to share a few characteristics. The medication involved is one known to carry serious risks that require active management. The patient reported symptoms or concerns that were documented or provably communicated, and the provider failed to respond. The harm that followed, whether organ damage, a dangerous drug interaction, or a worsening condition, is something a reasonable physician monitoring the patient would have caught and addressed.

The best cases also have clear medical records that tell a story. Evidence may include medical charts, nursing notes, alarm system data, and expert testimony from specialists. When the records show long stretches of time with no follow-up, no lab orders, and no documented patient contact after a high-risk prescription was written, that absence can itself become evidence of a problem.

Weaker cases typically involve side effects that were properly disclosed upfront, where the patient was informed of the risks and the physician did conduct reasonable follow-up, even if the outcome was still bad. Rhode Island law does not hold doctors to a standard of perfection. Violating standards of care means a doctor or hospital makes a mistake that another qualified medical professional would not have made under similar circumstances. That distinction matters. A bad result is not, by itself, malpractice.

The informed consent angle also comes into play. Rhode Island requires a five-part test to decide if there is validity in a medical malpractice case surrounding a lack of informed consent, including whether the physician’s explanation of risk was inadequate, the risk was known and withheld, the risk was a valid concern, and the injury was caused by this undisclosed risk. If a physician never warned a patient about a known side effect that later caused serious harm, that failure can support a separate but related legal theory.

The Timing Question Comes Up Often

About those filing deadlines. This is an area where we encourage clients to reach out early, because the window to act is not unlimited.

Rhode Island’s standard medical malpractice statute of limitations gives an injured patient three years from the date of the alleged malpractice to get the case filed in court. That sounds like plenty of time, but medication side effect cases can complicate the calculation. Harm from a medication sometimes develops gradually. A patient may not connect a worsening condition to a prescribing failure until well after the problem began.

Rhode Island law does account for this. Rhode Island applies what is called the discovery rule, which is an exception to the standard deadline in situations where injured patients could not reasonably have learned that they had a medical malpractice case. The clock starts when the patient knew or reasonably should have known about the harm and its connection to the provider’s conduct.

The thing about the discovery rule, though… actually, the important nuance here is that relying on it requires proof. If you are relying on the discovery rule to extend the statute of limitations, you have the burden of proving that you did not discover and could not have discovered the malpractice any sooner than you did. That is a legal argument that needs to be built carefully, which is another reason early consultation with an attorney matters.

Expert Testimony Is Not Optional

Frankly, one of the most important things to understand about medication monitoring cases in Rhode Island is that they almost never succeed without qualified medical expert testimony. The injured party must present testimony from a medical expert to prove that a healthcare provider breached their duty of care. Rhode Island law further requires that only those with knowledge, skill, experience, training, or education in the field of the alleged malpractice may qualify to give that testimony.

This is not a technicality. It is the foundation of the entire case. An expert witness establishes what the standard of care was, how the defendant’s conduct fell short, and why that failure caused the patient’s specific harm. Without that connection, even a sympathetic set of facts may not be enough.

We work with qualified medical professionals who can evaluate these cases and provide credible testimony. That process takes time, which circles back to the earlier point about not waiting too long to seek legal guidance.

What Compensation May Look Like

Rhode Island is one of the states that does not cap damages in medical malpractice cases against private providers. Rhode Island has no statutory cap on damages in medical malpractice cases, so a judge or jury is free to award any amount they see fit when a healthcare provider is found liable. That means compensation in a successful case may cover medical expenses related to the harm caused, lost income, pain and suffering, and other losses that are documented and proven.

We want to be clear that no attorney can promise a specific outcome. Every case turns on its own facts. What we can say is that Rhode Island’s legal framework gives seriously injured patients a genuine opportunity to pursue accountability when a provider’s failure to monitor medication side effects caused real harm.

Reach Out Before Time Runs Out

Most people hire lawyers too late. By then, records have been lost, memories have faded, and legal options have narrowed. If you or someone you love experienced serious harm that may be connected to a physician’s failure to track or respond to medication side effects, we encourage you to contact DeLuca, Weizenbaum, Barry & Revens, Ltd. for a free consultation. We have been serving Rhode Island families for over 40 years, and we are here to help you understand what your situation may mean under the law.

This blog post is intended for general informational purposes only and does not constitute legal advice. Every situation is different. Please consult with a qualified attorney about the specific facts of your case.

Attention-deficit/hyperactivity disorder (ADHD) diagnoses are becoming increasingly common among children today. With this rise in diagnoses, it is important to carefully consider the right treatment for each child. Unfortunately, some children may receive medication that they do not need. What should parents know?

ADHD diagnoses and medications are becoming more common

Statistics show that about one in ten children between the ages of 5 and 17 have received an ADHD diagnosis. Because of this increase, doctors often prescribe medications like Ritalin and Adderall to treat ADHD. These medications can be effective, but they can also have serious side effects like sleep disturbances, decreased appetite and mood swings.

Unfortunately, rising ADHD diagnoses have also led to a rise in mistakes involving these medicines. One study found that reports to poison centers related to ADHD medication rose by 300 percent between 2000 and 2021.

Is this medication necessary for every child?

There are concerns that some children might be receiving higher doses of medication than they need or unnecessary medication. Sometimes, children who might not fully meet the ADHD criteria are given medication. In other cases, healthcare providers might choose medicine as a quick fix instead of trying other ways like therapy, counseling or lifestyle changes.

Parents and healthcare providers need to work together to ensure the ADHD diagnosis and treatment plans are right for each child. This means doing careful assessments, watching progress and considering non-drug options as part of the treatment. If not, medicines meant to help could actually harm.

You can protect your child from overmedication

Medicine can be very helpful for managing ADHD symptoms, but it is important to stay balanced and avoid giving too much. If you think a doctor has given your child ADHD medication unnecessarily, consider getting a second opinion and talking to a medical malpractice attorney. They can help make sure your child gets the care they really need to succeed.

Healthcare professionals have numerous tools that their disposal. They often work with corporate medical practices or hospitals where they can refer patients to specialists. They may have access to diagnostic equipment and rehabilitative facilities.

Additionally, physicians can prescribe thousands of different medications to help people address the symptoms of a medical issue. Prescription drugs can help with everything from blood pressure to nausea. Typically, any medication available on a prescription basis has undergone testing to ensure that it is reasonably safe and effective for the treatment of certain medical conditions.

Can doctors prescribe a medication for a purpose other than its intended use, or is this effort a medical malpractice lawsuit waiting to happen?

Off-label prescribing is a common practice

The Food and Drug Administration (FDA) reviews data collected by pharmaceutical companies as they develop their drugs. The companies typically fund the research that helps establish whether a new medication is reasonably safe and if it is more effective than a placebo to treat certain symptoms.

If the FDA approves a drug for one purpose, physicians can assume that the drug is overall safe for people to use. They could theoretically prescribe that medication to a patient for a completely different medical challenge. For example, in recent months, there has been a surge of interest in using certain diabetes medications to help people with intentional weight loss.

With that said…

Off-label prescribing is not automatically an act of medical malpractice. However, it can lead to claims of medical malpractice in certain scenarios. For example, medications may have warning labels advising physicians not to use the medication to treat certain types of people or specific medical conditions.

If a doctor’s off-label prescribing violates FDA warnings, then their choice to prescribe that medication could constitute malpractice. Similarly, the decision to use a drug for an off-label purpose when another, potentially safer drug can achieve the same goal might constitute malpractice. The degree of risk for the patient and whether another reasonable physician would have prescribed the same medication are the main considerations in such cases.

A patient’s awareness of the risks can also play a role in whether or not malpractice has occurred in the event of medication-related harm. Physicians should generally warn patients about failure rates, side effects and contraindications when using a medication for an unapproved or experimental purpose. Reviewing medical records and current best practices can help someone determine whether a medication error or other adverse event that they have experienced constitutes malpractice or not.

Whether you just picked up some medication at the pharmacy or are currently receiving inpatient care at the hospital, you expect that the medical professionals providing your support will do so in a professional manner.

However, even the most experienced and dedicated healthcare worker is only human. They may come to work when they have a migraine or feel distracted and fatigued at the end of a long shift. Issues ranging from distraction to labeling errors could affect the medication a patient receives.

Regardless of the reason why it occurs, a healthcare professional making a mistake during the administration of medication could lead to one of the four negative consequences for a patient listed below.

  1. A dangerous drug interaction

Some medications respond dangerously to the presence of other chemicals in your bloodstream. One drug may have a synergistic effect with another, meaning that they amplify each other’s impact on the body. There are also drugs that cancel one another out or that create completely new physical consequences when combined with one another. When healthcare professionals administer the wrong drug to someone, it may interact with another medication they have recently taken.

  1. An overdose

Excess medication can cause harm to the human body. Having too much of certain active compounds in a patient’s bloodstream can damage their renal system, for example. A medication mistake where someone receives the wrong drug, the wrong dose or the right medication at the wrong time could potentially lead to a severe injury or fatality related to overdose.

  1. Reduced treatment effectiveness

A mistake regarding the drugs that someone receives might mean that the treatment they undergo is less effective than it would otherwise be. Missing doses of an antibiotic, for example, might mean that the bad bacteria continue to procreate and put someone at risk.

  1. Severe side effects

Some medications are known to have major side effects, and those side effects can be particularly severe if someone takes other medication or has certain underlying health conditions. A patient who receives the wrong medication could develop long-term side effects, such as damage to an organ, as the result of receiving the wrong drug.

Any of these consequences could lead to poor outcomes for patients and increased medical costs. Pursuing a medical malpractice claim may be an option for someone harmed by a medication error in a professional environment.

In the medical industry, it’s called “drug diversion,” which sounds pretty innocent. But it means stealing and abusing medication, usually powerful painkillers, meant for patients.

Unfortunately, healthcare professionals are not immune to the risk of drug addiction. But their access to drugs can lead to serious incidents of medical malpractice.

How medication theft endangers hospital patients

One of the biggest dangers comes in when these doctors, nurses and others with access to medication try to cover their tracks. As an expert on the problem explained to NPR, a worker might steal a vial of fentanyl from their hospital’s supply cabinet. After using the drug on themselves, they replace the liquid fentanyl with water.

If a nurse administers the vial to a patient, the patient could contract a serious, chronic disease. For example, a study by the Mayo Clinic found that up to 28,000 patients were potentially exposed to Hepatitis C over a decade due to drug diversion and the use of unclean needles. Imagine being diagnosed with a serious disease because a medical professional injected you this way. Or that you are in the hospital, needing a specific medicine, but there is not enough to save your life because someone falsified the inventory records.

The size of the problem is unknown

The extent of drug diversion in America’s hospitals may never be fully known. But it obviously happens often enough that you cannot guarantee you won’t be affected someday. Addiction can take over a person’s life, but that is no excuse for neglecting the health and safety of your patients. The stakes are simply too high.

Lyme disease is an illness caused by a bacteria carried by ticks. The disease can cause severe headaches, neck stiffness, arthritis, joint pain, facial palsy and problems with short-term memory. Rhode Island is one of 14 states with Lyme Disease-carrying ticks and is a hotspot for Lyme disease cases. Pharmacies have expanded their role in prescribing medicines across the state under what is called collaborative practice agreements and are now able to give doxycycline to patients who have been bitten by ticks within a 72 hour window. Some feel that pharmacist error in diagnosing and assessing the tick bite will lead to increased antibiotic resistance.

The new program allows individuals who have been bitten by a tick to come into a pharmacy and receive a dose of the antibiotic without a prescription after answering questions about the tick and their condition. The patient will choose the tick that bit them from a chart of potential disease-carrying types of ticks. The pharmacy should follow CDC guidelines for Lyme disease assessment.

In some cases, the individual seeking treatment did not bring in the tick or a picture of the tick when choosing the tick from the poster. Opponents argue that the evidence used to claim that doxycycline can prevent Lyme disease is weak. From a public health standpoint, overprescription of antibiotics leads to widespread antibiotic resistance.

How will pharmacists in Rhode Island be held accountable to the standards? Does the pharmacist have a role to play in pharmacist error if a person receives the antibiotic without showing evidence of the tick? A pharmacy error can cause harm to an individual’s health. If a person has been harmed by a pharmacist’s error, a personal injury attorney can assist with filing a claim for monetary damages.

Most in Providence County may tell you that drug errors occur when a healthcare provider gives a patient the wrong medication. While this certainly may be among the more common types of medication mistakes, the truth is that drug errors can occur any number of different ways. Almost as important as receiving the right drug is being administered the recommended dosage at the correct concentration. Beyond that, the administration route must also be considered. What are drug routes? They are the various methods through which a medication is introduced into your body.

If you are like most, then you envision a medication administration as you popping a pill into your mouth. Yet the website Healthline.com actually lists several different drug routes that providers may utilize. Listed below are the various methods through which drugs are dispensed:

  • By mouth: Oral pills or liquids, sublingual medications, buccal drugs (held inside the cheek)
  •  By nasal passage: inhalants, nasal sprays, nebulizer treatments
  • By injection: intramuscular or subcutaneous injections
  • By skin: transdermal patches, topical ointments
  • By delivery mechanism: intravenous infusions, enteral administrations via a G- or J-tube
  •  By other body openings: eye drops, ear drops, rectal suppositories

Why is the route through which a medication is delivered important? The method through which a drug enters the body influences how much or how strong of a dosage you will receive. For example, if your doctor wants a medication to have an instant effect, he or she may choose to introduce it directly into your bloodstream rather than having it metabolize through your liver. An overly concentrated dose could then have catastrophic effects due to it not having been detoxified through metabolism. Along the same lines, a diluted dose given orally may not allow the drug to serve its purpose, thus prolonging your pain and suffering.

Many in Providence County, after having been written a prescription by their doctors, may go to their local pharmacies fully expecting those orders to be filled correctly. To prevent errors from happening, pharmacies may even have safeguards in place such as computer systems that warn them they may be dispensing the wrong medication. Yet even with added measures such as these, medication errors continue to happen. When they do, one’s only logical conclusion when trying to explain such mistakes may be to attribute them to human error.

That’s the claim that is being made in lawsuit filed by an Ohio man. The man received what he believed was high blood pressure medication from the pharmacy at a local Kroger store in late 2013. Shortly after beginning to take the medication, we began to experience disorientation and vomiting to the point of becoming severely dehydrated. He was eventually hospitalized and diagnosed as being in renal failure. After having the medication examined by another pharmacist, his wife discovered that he had actually been given an anti-seizure medication by the Kroger pharmacy.

A review of the Kroger pharmacy’s records showed that one tech assumed after looking at the pills that the order was correct due to the fact that both medications looked similar. Another was shown to have overridden the pharmacy’s computer system after it alerted him that the medication was incorrect.

A failure to adequately ensure that medications are correct or to heed to warnings given by verification systems may certainly be seen many as negligence. Those who suffer because of such negligence may wish to speak to an attorney to discuss what their options may be in pursuing legal action.

Source: WXIX “Man claims wrong medication from Kroger accelerated kidney failure” Baldwin, Michael, Aug. 14, 2016

Most people in Providence County would likely associate errors involving a patient’s medication to instances where he or she was either given an incorrect dosage of a prescribed medication or administered the wrong medication altogether. While such errors certainly rank among the more common types of medication errors, another less-apparent yet potentially as damaging a mistake is a medication omission. The American Society of Health-System Pharmacists defines an omission error as “the failure to administer an ordered dose to a patient before the next scheduled dose, if any.”

Medications prescribed to attack infectious agents or assist with a course of treatment may be vital in producing positive patient outcomes. Thus, the omission of a medication could very well be just as serious as too much of it being given. One may wonder how it can be possible for a clinician to overlook the administration of medication (particularly those administered intravenously) given the many delivery methods and protocols in place to account for them. A study undertaken by the Pennsylvania Patient Safety Authority revealed the following to be among the most common reasons why IV medications were never given:

  • IV medications not sent with patient during transfer, or not being connected, hung, or started upon his or her arrival in a new unit.
  • IV pumps or drug delivery systems never being activated.
  • IV lines becoming occluded or being mistakenly clamped.
  • IV’s being accidentally discontinued or stopped.
  • Empty or defective IV bags not being replaced.
  • Nurses becoming distracted.

To prevent omission errors, the ASHP strongly recommends nurses stick to scheduled administration times and document any refusals by a patient to take a prescribed medication or any medication availability issues. A lack of such documentation in a patient’s medical record could be seen as evidence a required medication was never given.

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