Pharmacovigilance
Pharmacovigilance
Adverse Drug Reactions (ADRs)
Pharmacovigilance plays a vital role in ensuring the safe and effective use of medicines. According to the World Health Organization (WHO), pharmacovigilance is the science and activities concerned with the detection, assessment, understanding, and prevention of adverse effects or any other medicine-related problems.
As healthcare systems evolve, maintaining patient safety and public confidence in medicines has become increasingly important. Pharmaceutical and biotechnology companies are responsible not only for monitoring the safety of their products but also for continuously evaluating and managing potential risks throughout the product lifecycle—from research and development to post-marketing surveillance.
Drug Safety
Adverse Event Reporting
At Emmwell, patient safety is our highest priority. If you experience or become aware of an adverse event associated with any of our products, please report it by completing the Adverse Event Reporting Form and sending it to: info@emmwellpharma.com
Adverse Event
What is an Adverse Event?
An adverse event is any unintended or undesirable medical occurrence experienced by a patient following the use of a medicinal product. Such events may or may not be directly related to the medicine and are commonly referred to as side effects.
Why Report an Adverse Event?
Reporting adverse events helps us continuously monitor the safety of our medicines and improve patient care. Your report can contribute to the identification of:
- Rare or previously unknown adverse reactions
- Unexpected side effects
- Drug-drug or drug-food interactions
- Potential risk factors associated with medicine use
- Long-term safety information
This information supports the ongoing evaluation of medicine safety and helps protect public health through timely identification, assessment, and management of safety concerns.
What Should Be Reported?
Please report any adverse event or side effect experienced after the use of an Emmwell product, regardless of its severity or whether you believe it is related to the medicine.
Where to Report?
Confidentiality
The privacy and confidentiality of all patients and reporters are strictly maintained. Personal information provided in adverse event reports is protected in accordance with applicable privacy regulations and company policies. Emmwell will not disclose the identity of the patient or reporter to the public.