A bill has been introduced into the Senate that would allow the US Food and Drug Administration the ability to recall medications that are unsafe for consumers. Currently, the FDA is only allowed to recommend a recall rather than initiate it.
The FDA publishes safety alerts for both prescription drugs and over-the-counter medications that may be unsafe. Also included in this list are products that are regulated, such as hand sanitizer. An example of the need for this kind of intervention came about in recent months when the FDA issued a recommendation that more than 100 hand sanitizer products be recalled because they contained a toxic chemical known as methanol. Some of the companies did not comply with the recommendation.
The bill was introduced by Senator Gary Peters who is a Ranking Member of the Homeland Security and Governmental Affairs Committee. Known as the Safe Drugs Act, many health care providers, hospitals and other facilities back the bill. While most companies generally follow the FDA recommendations and issue a voluntary recall, some companies in recent past have failed to do so, which many organizations believe put consumers at risk.
Hand Sanitizer Recall
In recent months, several recall notices have been posted for medications and drug-related products. One of the most well-known is the hand sanitizer issue. What started at around 100 products has now expanded to almost 200 items. According to the FDA, if someone were to drink the hand sanitizer or swallow it, they could have serious health issues, including blindness and even death.
The need for hand sanitizer has exploded with the recent pandemic. As a result, many companies rushed to capitalize on the situation and brought a new product to market. However, many of them are unsafe. These products can be found online as well as in major retailers like Walmart, Target and other national chains.
Along with the danger of swallowing, methanol is also toxic if it is absorbed into the skin, which would certainly happen with hand sanitizers. Many of the manufacturers are based in Mexico, but some products were made in the US.
An import alert was issued earlier this year to prevent the products containing methanol from entering the US. The agency also warns not to be fooled by products that claim to be FDA approved as none have been. They also say to be wary by products that say they can protect a person for up to 24 hours, as this is untrue as well.
As this issue indicates, the FDA has limited authority to stop products from being sold that are dangerous to consumers. However, new legislation would give the agency more authority to remove unsafe products. Several people have died from the hand sanitizers that were part of the alert. The bill has not been passed as of yet due to the Senate’s recess.
Until given more authority, the FDA will continue to monitor drugs and other products on the market and test them for safety. Any found to be unsafe will result in a recommendation for a recall.
Recall for Drug Mix-up with Serious Effects
A factory mix-up of two very different medications has drug manufacturer, AvKare, issuing a recall. The factory packaged two different medications in the wrong bottles. One is an antidepressant, and the other is a medication used to treat erectile dysfunction.
Details of the Recall
The first medication is trazodone, used as a sedative and to treat depression. The second medication was sildenafil, for erectile dysfunction issues. The medicines were accidentally packaged in the opposite bottles by a third-party manufacturing facility.
The manufacturer is urging anyone with either of these medications to stop taking them. If someone is prescribed the sildenafil for ED, they could notice symptoms, such as blurry vision or dizziness and sedation. For the patient who is taking trazodone, they won’t get the help they need for depression. The medication might interact with other medications they might be on. Sildenafil is not to be taken with nitrates, which are commonly given for heart disease or diabetes.
AvKare has provided notification to the distributors and customers. The company is making arrangements to have all recalled products returned. Both medications are listed at 100mg. Taking sildenafil by accident can cause the blood pressure to drop to a dangerous level. At this point, no reports of adverse reactions have been reported.
To know if your product is part of the recall, you can heck the lot number and expiration date. The sildenafil 100mg tablets are Lot 36884 which expire 03-2022. The trazodone hydrochloride 100mg tablets are lot 36783, and they expire 06/2022. If consumers have questions, they can call 855-361-3993 on Monday through Friday between 8AM and 4PM CST.
The Dangers of the Medications
While AvKARE is based out of Pulaski, Tennessee, the drugs were distributed around the country, according to the US Food and Drug Administration. The risk of adverse side effects is higher for older patients who are already at an increased risk for falls. It can also impair driving.
Patients who have been prescribed the medications that are affected by the recall should contact their medical provider. They will need to get a new prescription to treat their conditions, especially for those who are taking trazodone for depression. They may notice that the medicine they are using isn’t having the same positive impact on their health because they have been given the wrong medication.
Trazodone works to treat insomnia as well as depression. However, it isn’t approved by the FDA for insomnia. It is believed to inhibit the uptake of the hormone serotonin in the brain. Ironically, one of the side effects of this medication is sexual dysfunction, along with headache, constipation or diarrhea. If abruptly stopped, it can lead to anxiety and disturbances with sleep. That’s why it is important to speak with a doctor if you discover you’ve been taking medication which is part of the recall. This medication can also cause drowsiness and the ability of the person to drive a vehicle or operate other types of machinery.
If you have been taking the medication from the recalled lot, you should seek medical attention if you notice any adverse symptoms.
Moderna Seeks Emergency Approval for COVID Vaccine
Moderna has completed phase 3 of a study on a COVID-19 vaccine. It was found to be over 94 percent effective for 30,000 participants. Based on the data from this study, Moderna plans to file what is known as an emergency use authorization or EUA with the Food and Drug Administration.
Of those in the vaccinated group, only 11 people tested positive for COVID-19 after taking the vaccine compared to 185 participants who were in the placebo group. Moderna also made the announcement that the vaccine prevented more serious cases of COVID-19. The 30 severe infections were found in the placebo group.
The FDA will review the data on safety and efficacy from Moderna at its VRBPAC meeting (Vaccines and Related Biological Products Advisory Committee), which is currently scheduled to be held on December 17.
According to a spokesperson with Moderna, the data confirms the ability of the vaccine to prevent COVID-19, especially severe cases. The goal of the vaccine is to prevent severe outbreaks of the disease as well as hospitalizations and death in those who contract the virus.
The efficacy of the vaccine was consistent in groups based on gender, age and ethnicity. The Modern trial included people who were over 65 years of age as well as participants from 42 communities, such as Hispanics, Asian Americans and African Americans. There were also participants who were multiracial.
No Concerns Over Safety
According to data from Moderna, participants tolerated the vaccine well with no serious concerns identified. The most common issues noted included fatigue, pain at the site of the injection, headaches, redness at the site, myalgia, and arthralgia. The frequency of the complaints increased in frequency and severity after the second dose of the vaccine were given. The only COVID-19 related death in the study came from the participants in the placebo group.
If the vaccine is approved by the FDA, Moderna has said it can have about 20 million doses ready to ship in the US by the end of 2020. It expects to manufacture between 500 million and 1 billion doses for around the world in 2021. Moderna is seeking approval from other organizations globally. It will be the second company to request an EUA with the FDA for a vaccine with Pfizer being the first.
As a vaccine reaches approval, the government will likely determine how it will be divided up. Some experts suggest the vaccine will go the states with the highest populations. It has also been suggested that a separate vaccine will be necessary for children and this first one approved will be for the adult population.
As more cities initiate greater restrictions and even lockdowns or stay-at-home orders, the need for a vaccine becomes more apparent. The fact that two such vaccines are close to being ready for use provides welcome news to the medical industry as well as the general population, especially as the holidays approach and flu season continues to be a concern.
Z-Drugs Increase Risk for Fractures in Dementia Patients
According to a new study, dementia patients who are prescribed Z-drugs at higher doses may have more of a risk for fractures and falls as well as for strokes. These medications include zalepion, zopicione and zopidem.
According to the experts, z-drugs should not be prescribed to patients with dementia. The risks are even higher than those who take higher doses of benzodiazepines. Originally, the z-drugs were thought to be safer than benzodiazepines. However, new evidence shows this isn’t true.
Details of the Study
The study took a look at z-drug prescription use and the following risk for falls, factures, infection, ischemic stroke, venous thromboembolism and death. All 27,000 patients were diagnosed with dementia sometime between January 2000 and March 2016. They compared those results with people who didn’t use the medications who had sleep disturbance, as well as new users of benzodiazepine of similar age, sex and use of antipsychotics.
Of the total number of dementia patients started on z-drugs, almost 20 percent of them were given higher doses. Within that group, those patients showed a significant increase in the risk for fractures, as well as hip fractures specifically and falls in generally. The research also showed a higher risk for ischemic stroke over those who didn’t take sedatives and had sleep disturbances.
The risk was minimal or inconsistent when looking at those who were taking z-drugs at a lower dose. There was no evidence of increased risk for infection, death or VTE in patients prescribed higher doses of z-drugs. Information gleaned from the study also showed that those patients who were taking z-drugs at higher doses were more likely to be admitted to a hospital or see a doctor. They may also receive more prescriptions for antidepressants, antipsychotics and antibiotics.
Sedatives and Dementia Don’t Mix
Researchers say that this information indicates the dangers of prescribing sleeping medications to people who have been diagnosed with dementia. Those involved in this study also say this data is timely in showing that sedatives aren’t a good way to deal with social isolation from COVID-19. The experts also say the need is great to improve sleep management treatments.
Experts say that if sedatives are necessary for dementia patients, they should be time-limited. Other components of sleep management include reviewing other medications they may be taking which could contribute to sleep issues and improving sleep hygiene. Anyone who is taking z-drugs with dementia shouldn’t stop, but they should talk to their doctor about tailoring off of them.
While the study may not show new information, it strengthens the association between sedatives and risks for dementia patients. Experts say that it has long been suspected that giving dementia patients sedatives isn’t a good idea. However, you can’t determine the cause with this study, only the association.
Falls and fractures are a concern for many older people, especially because they are likely to take longer to heal. When an elderly person suffers a fracture, it may not heal as well. In many cases, they may be unable to stay by themselves even after they recover.
Defective Products11 months ago
Dehumidifier Recall: Several Brand Name Humidifiers are Recalled as a Fire Hazard
Medical Devices2 years ago
Complications from Hernia Mesh
Covid-192 months ago
Moderna Seeks Emergency Approval for COVID Vaccine
Covid-195 months ago
Metformin as Potential Protector from COVID-19
Prescription Drugs1 month ago
Recall for Drug Mix-up with Serious Effects
Defective Products1 year ago
Toyota Has More Safety Recalls
Covid-196 months ago
FDA Adds Nearly Two Dozen Drugs to Watch List
Birth Defects4 months ago
New Data Links Antidepressants to Birth Defects