
Abbott’s weight-loss drug Meridia increases the risk of stroke and heart attack in patients with heart disease, according a study …

From September all serious adverse events that occur during clinical trials in the UK will have to be reported electronically …
The US medicines regulator is to make safety reviews of recently approved prescription medicines more readily available to the public. …
Boehringer Ingelheim has given a robust rebuttal to a Lancet report implicating its hypertension drug Micardis (telmisartan) in scares about …
The US Food and Drug Administration has taken the advice of its advisors and given its backing to resume the …
FDA advisors have recommended two rotavirus vaccines licensed in the US should continue to be used, despite contamination with a …
Pharmaceutical and medical device recalls more than quadrupled in the UK between 2004 and 2008, with the majority caused by …
The pharmaceutical industry is ready to adapt to growing drug safety requirements, but understanding of how it can capture safety …
Adverse drug reaction in hyperactive children has been made a key research priority for next year by the European Medicines …
The new head of US regulator the FDA has set out a vision to support public health, through tighter laws …
Pfizer and GSK's smoking cessations drugs will have to carry strong warnings of depression and other mental health adverse events …
How did you find your way into your current role?From the age of 11 I wanted to be a farmer. …
This year is a bit of a jamboree of health-related anniversaries, with the NHS celebrating 60 years and the Medicines …
There is a tide of change in drug safety within the pharmaceutical industry. Internal and external forces are pushing drug …