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Drug Safety Data Underscores Need for Pharmacovigilance

May 16, 2017

One in every three new drugs triggers side effects discovered only after Food and Drug Administration approval, new data reveals.  And that statistic begs a crucial question: How can we really ensure patients’ safety in an age of sophisticated medications and accelerated approval processes?

Access Issues Loom Large at Munich Workshop on Biologics and Biosimilars

May 10, 2017

When should patients switch from one medicine to another for non-medical reasons?  How can pharmacovigilance processes successfully monitor patients’ reactions to a medicine? And, perhaps most importantly, how do we ensure that patients are informed participants in decisions about their medication?

Tubing Mix-ups Pose New Dangers for Infants

April 25, 2017

Robin Rogers was 35 weeks pregnant when she began to suffer from significant vomiting and dehydration. She was admitted to the hospital near her home in Kansas. To correct her fluid and nutrition levels, Robin had two tubes placed: one, a feeding tube; the other a PICC line, often used to draw blood or deliver antibiotics.

Summit on Biologics and Biosimilars Tackles Choice, Switching & Patient Access

April 10, 2017

Physicians and patients are no longer asking if a biological medicine is the best choice, but – more likely – which biological medicine is the best choice.  This opening thought from Alliance for Patient Access Chairman David Charles, MD, set the tone for the organization’s second annual National Policy and Advocacy Summit on Biologics and Biosimilars, held Thursday in Washington, DC.