reporting side effects

the .gov means it’s official.federal government websites often end in .gov or .mil. the https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. if you think you or someone in your family has experienced a serious reaction to a medical product, you are encouraged to take the reporting form to your doctor.




however, we understand that for a variety of reasons, you may not wish to have the form filled out by your health care provider, or your health care provider may choose not to complete the form. your health care provider is not required to report to the fda. you will receive an acknowledgement from fda when your report is received. clinically important and timely information about the drugs and devices you use, prescribe, or dispense every day, delivered to your email from the fda.

information and tools for investors including share and dividend information, share price analysis, latest news and corporate reporting science can improve health and well-being in so many ways, from the development of everyday healthcare products to medicines and vaccines. we want to help change this, using our scientific expertise, our partnerships and our global reach. the subsequent websites and web pages are intended for non-uk audiences. at gsk we take the safety of our patients and consumers very seriously.

for this reason, it is vital for us to continuously monitor the safety of our products. at a minimum you will need to provide the following: our privacy notice outlines how gsk handles the processing of personal information when dealing with your enquiry, complaint or adverse event report. information and tools for investors including share and dividend information, share price analysis, latest news and corporate reporting this is our global website, intended for visitors seeking information on gsk’s worldwide business. trade marks are owned by or licensed to the gsk group of companies. registered in england and wales no.

important: if you are experiencing a medical emergency, seek immediate assistance from a healthcare provider or call 9-1-1. cdc and fda do not provide report serious adverse events for human medical products, including potential or actual product use errors, product quality problems, vaers is the national vaccine safety monitoring system that accepts reports of adverse events after vaccination. the system can quickly detect potential, .

vaers is an early warning system used to monitor adverse events that happen after vaccination. learn how vaers reports are submitted and reviewed. if you experience an adverse event (not a side effect) from one of our drugs, tell your doctor and then report it to us. this helps us track the safety of this includes review of safety data from clinical studies and review of side effects and technical complaints. by monitoring quality and safety information, .

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