Looking for information about specific medicines?
There are many valuable resources available to help you learn more about the benefits and risks of specific medicines or medical treatments.
To learn more about medicines prescribed in the United States, visit:
U.S. Federal Drug Administration (FDA) Web site
Go to FDA Drug Index
The Physicians' Desk Reference Web site
Go to www.pdrhealth.com
To learn more about a specific Pfizer medicine, visit:
The Pfizer.com Product page
Go to Pfizer Products
If you live outside the U.S., please consult your local regulatory agency's Web site for safety information about specific medicines prescribed in your country.
Reporting Side Effects
Important Note: Patients should always ask their doctors for medical advice about side effects.
How to report a side effect in the United States
The U.S. Food and Drug Administration (FDA) has established a reporting service known as Medwatch. Through this service, health care professionals and consumers can report serious problems they suspect may be associated with the drugs and medical devices they prescribe, dispense, or use.
You may also report side effects by phone to either of the following toll-free numbers (U.S. only):
- FDA: 1-800-FDA-1088 (for side effects related to any U.S. product)
- Pfizer Inc: 1-800-438-1985 (for side effects related to Pfizer products)
Outside the United States
To report a side effect, contact your local health authority or ask your health care provider for more information. Countries worldwide have unique processes in place to handle reports of side effects.
Medicine Safety Education
A resource for health care providers and patients
Part of our responsibility as a global pharmaceutical company is to help keep the patients who take our medicines safe. At Pfizer, our commitment to medicine safety begins in the research laboratory—and continues for as long as the medicine is prescribed to patients anywhere in the world.
As part of this commitment, we have developed this interactive educational section in pfizer.com to help health care providers, public health professionals, patients, and caregivers learn more about medicine safety. "Understanding Risk", "Medicine Safety Timeline", and "Partnering to Protect Patients" have been developed for professional audiences. "Medicine Safety for Patients" has helpful information developed especially for patients and caregivers.
Choose the section of the site you would like to visit by clicking on an image below.
Looking for information about specific medicines?
Medicine Safety Video Hosts
(select a section)
> Next: Click to Get Started
Understanding Risk
Like many aspects of life, taking medicine involves benefits and risks. But often, the benefits medicines provide to our health outweigh the potential risks. Learning more about risk—and how to put it in perspective—can help both patients and doctors make important decisions about health and treatment.
In this section, you will explore the fundamentals of risk:
- Perceiving risks: Learn more about factors that affect risk perception—and why perceptions about risk may not always reflect the actual risk involved.
- Viewing risks: Take an in-depth look into the statistics used to evaluate risk.
- Monitoring evolving risks: Find out how pharmaceutical companies and regulators weigh benefits and risks when making decisions about medicines.
> Next: Perceiving Risk
Medicine Safety Timeline
Medicine safety: An ongoing process
Patient safety is a paramount concern throughout the life of a medicine—and pharmaceutical companies have ethical and regulatory responsibilities to monitor the safety of the medicines they sell for as long as they are used by patients anywhere in the world.
Explore this section to view how safety is integrated into every phase of testing and development, and how efforts to manage potential safety issues in approved medicines continue for many years.
An important note for patients
Please note that all are welcome to explore the medicine safety timeline. However, this section is intended primarily for health care professionals.
Partnering to Protect Patients
All medicines have benefits and risks—and individual patients react to medicines differently. That is why patients must work with their doctors to carefully weigh the benefits of a medicine against its risks for their individual situation—and make the choice that's right for them.
To help protect patients, an extensive network is in place to identify and manage possible safety concerns associated with the medicines they take.
Click on the connection between any of the two images below to see how each partnership works as part of the larger network.
To view this interactive feature, you must have Flash 9 installed on your computer.
If you do not have Flash 9, you can download it from the Adobe web site.
An important note for patients
Please note that all are welcome to explore this section. However, some of the information provided here is intended primarily for health care professionals.
Next: > Regulatory Agencies & Industry
Your Role in Medicine Safety
When it comes to taking medicine, you play an important role in ensuring your safety—and the safety of those you care for. By partnering with your doctor and other health professionals involved in your care, you can help them determine which medicines are most appropriate for you or your dependents. Partnering also helps your health care professionals teach you how to take these medicines safely.
In this section, you'll learn how to reduce your risks of medication safety problems at key points in your care:
- At your doctor's visit
- When you fill your prescription
- When you take your medicine
- After you take your medicine
Who plays a role in medicine safety?
- Pharmaceutical companies that develop, test, and produce medicines
- Regulatory agencies that approve the use of medicines—like the U.S. Food and Drug Administration (FDA) or European Medicines Agency (EMEA)
- Doctors and other health care professionals who prescribe medicines
- Patients and caregivers who take medicines or give medicines to those they care for
What is involved in approving a medicine?
All medicines have benefits as well as risks. Before any new medicine is approved by regulatory agencies such as the EMEA or FDA, it undergoes extensive testing—usually in several thousand people. The goal of this testing is to determine how safe and effective the medicine is—and to show that its benefits outweigh the known risks. A medicine is approved for use by appropriate patients only when its benefits have been adequately shown to outweigh the risks for its intended use in those patients.
> Next: Partnering With Your Doctor
To view the video introduction on this page, you must have the latest version of the Flash Player installed on your computer. If you do not have the Flash Player, you can download it from the Adobe web site.
Welcome to our Medicine Safety Web site. This site is designed to help you learn more about the science, processes, and people involved in the work of understanding the risks and benefits of medicines.
As part of the global health care community, pharmaceutical companies work with regulatory agencies, health care professionals, and patients to understand, as precisely as possible, the risks and benefits of each medicine we develop. Information about medicine safety begins to emerge in the research laboratory—and continues to evolve for as long as the medicine is prescribed to patients anywhere in the world. That's why there are systems and processes in place at each step to help identify and communicate benefits and risks to everyone involved in making decisions about treatment.
Throughout this site, we will help you explore these processes as well as the science behind the research and development of prescription medicines. Look for the guide in each section of the site and press play for help in navigating through the information.
Resource Library
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The products discussed herein may have different product labeling in different countries.
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