Recall due to mismarked dosage cup in 4-oz bottles of Children’s Advil Suspension Bubble Gum Flavored.
The independent data monitoring committee (IDMC) concluded that the 2 trials (AMARANTH and DAYBREAK-ALZ) investigating the treatment in mild Alzheimer’s disease dementia, were not likely to meet their primary endpoints of change from baseline on the 13-item Alzheimer’s Disease Assessment Scale – Cognitive Subscale.
A physician report indicates that 4 placebo (non-hormonal) capsules were placed in the first 4 days of therapy instead of active capsules.
A number of kratom-containing dietary supplements are being recalled and destroyed by the manufacturer stated the US Food and Drug Administration.
After public opposition, the DEA has withdrawn its plan to classify the kratom plant as a schedule 1 substance.
Action taken after pharmacist found a heart drug among Effexor XR, FDA says.