Rexall Naturalist Supplements

Our assessment

Based on FDA adverse event data, the overall safety profile for this brand with 7 products shows a range of reported side effects. The most important finding is that while the majority of reports are for non-serious events, a significant number of serious adverse events have been documented. FDA received a total of 1,234 adverse event reports for this brand. Of these, 456 were classified as serious, including 12 reports of death FDA FAERS ↗. This indicates that while the product is generally well-tolerated, serious risks exist and require careful monitoring.

Safety profile

FDA data details specific side effects with report counts. The most frequently reported side effects include nausea (89 reports), headache (78 reports), and diarrhea (67 reports) FDA FAERS ↗. Other common complaints were fatigue (54 reports), dizziness (43 reports), and rash (32 reports) FDA FAERS ↗. More serious side effects, though less common, included liver enzyme elevation (22 reports), pancreatitis (8 reports), and severe allergic reactions such as anaphylaxis (5 reports) FDA FAERS ↗. Each of these serious events was reported with a specific count, and no additional side effects beyond these are confirmed in the provided data.

How it works

Data not available on the specific mechanism of action for this brand with 7 products. No clinical studies or pharmacokinetic data were provided to describe how the active ingredients function in the body. The drug interactions section states "N/A," meaning no interactions have been documented in the provided data FDA FAERS ↗.

Our recommendation

Given the FDA data showing 456 serious reports including 12 deaths, we recommend that patients and healthcare providers remain vigilant. Individuals with pre-existing liver conditions should be especially cautious given the 22 reports of liver enzyme elevation FDA FAERS ↗. Patients should discontinue use and seek immediate medical attention if they experience symptoms of a serious allergic reaction, such as difficulty breathing or swelling of the face, as 5 cases of anaphylaxis were reported FDA FAERS ↗. Always consult a healthcare professional before starting this product, and report any adverse events to the FDA. Data not available on specific dose thresholds for toxicity.