Inaccurate Medication Label Leads to an FDA Recall of These ADHD Pills

Should you take prescribed pills for a long time, you most likely get accustomed to doing so with no second thought in mind. Accordingly, you might not feel the necessity to check your medications every time you buy a new tablet, especially if the pills change in terms of packaging and label. 

Nonetheless, you must be vigilant because mistakes can occur, which is the current case for some tablets of ADHD pills and narcolepsy medication. These meds have been the subject of a recent FDA recall due to a mistake in medication label which took place during the process of manufacture. 

Read below for more insights on the most recent FDA alert prompted by public safety concerns!

1. ADHD Meds Withdrawn from Pharmacy Retailers’ Shelves

According to a present-date FDA alert, a manufacturing brand of medications meant to treat ADHD and narcolepsy, a sleep disorder, has voluntarily recalled a batch of tablets with a dosage of 30mg. 

The company in question is located in Massachusetts, where a pharmacist inspected a tablet of the ADHD meds in question, only to find an antihistamine drug. This paved the way for an inspection on the product that was distributed in multiple pharmacy retailers across the country.

2. Adverse Events of Taking the Pills with the Mixed-Up Label

Individuals who mistakenly consume the antihistamine drug instead of their prescribed pills can experience mild to severe adverse events. These may include dizziness, sleep disorder, depression, elevated ocular pressure, and thyroid, to mention a few.

Besides, not taking your prescribed pills can aggravate your symptoms and increase your complaints, resulting in a deterioration of basic organ functions in addition to an elevated risk of accident. 

People who need ADHD treatment or suffer from the sleep disorder narcolepsy must take their prescribed medication; otherwise, they risk getting injured owing to the sedating consequences of the antihistamine drug they unknowingly consumed.

In acute cases, the adverse events could lead to a fatality risk, notably if the patient participates in activities that they would only be safe doing if they regularly take their ADHD pills or narcolepsy medication.    

3. Inspection of the Medication Label Is Crucial for Public Safety

If you follow an ADHD treatment and you were prescribed the recalled products, you must double-examine your tablets, particularly if they are yellow, have a dosage of 30mg, and are labeled Zenzedi.  

They are generally delivered in white containers with a yellow “30”mg” foregrounded in the center. They usually have “30” on one side and “MIA” on the other, as opposed to the other meds, which have “211” on one side of the container and “GL” in the other corner.

The manufacturer has raised a public health alert to distributors and pharmacy retailers and warned them against selling the recalled products. Nevertheless, inspect your medicine cabinet and check if you have already purchased the pills in question. If you have them at home, take them back to the point of purchase immediately.

4. No Reports on Severe Adverse Events So Far

Public health was fortunately not jeopardized as no reports have been delivered to the manufacturer on severe adverse effects as of now. However, should you feel any sudden, unexpected symptoms following the consumption of your regular prescribed medication, inform health authorities without delay and stop taking the pills in question. 

Never think twice if you want to call your healthcare provider or ask your pharmacist should you have any concerns whatsoever. The FDA insists that public health is extremely important and nothing should compromise it or put it in risk.