- +963 99 596-3102
- Al Mansoura - Aleppo - Syria
- info@ibn-alhaytham.com
Pharmacovigilance: Our Commitment to Your Safety First
Ibn Al-Haytham Pharmaceutical Industries believes that the quality of medicine is incomplete without ensuring its safety. Therefore, we prioritize "Pharmacovigilance" as an integrated pharmaceutical system aimed at monitoring, assessing, understanding, and preventing all side effects related to medicines, in line with World Health Organization (WHO) standards.
What is Pharmacovigilance?
It is the science and activities relating to the detection, assessment, understanding, and prevention of adverse effects. Our role does not end when a drug is launched in the market; it extends to monitoring its performance under real-life clinical conditions and across a broad spectrum of patients to ensure the highest levels of clinical safety.
Our Objectives in Pharmacovigilance:
Our specialized team works toward the following goals:
- Early Detection: Monitoring any new or unexpected side effects as soon as they appear.
- Frequency Analysis: Monitoring the prevalence of side effects to assess the safety of continuous use.
- Risk Identification: Identifying predisposing factors for side effects to provide more accurate guidance.
Preventive Management: Implementing essential regulatory and medical procedures to minimize risks and promote a culture of safe use.
Understanding Side Effects
What is a Side Effect?
It is an unintended and harmful response resulting from the use of a medicinal product, whether at recommended doses, or due to misuse or overdose.
Why do symptoms appear that are not mentioned in the internal leaflet?
Medicines undergo extensive clinical studies before marketing, but these studies are conducted on limited numbers and for specific periods. Once a drug is released for general use, its effects appear on millions of patients over many years, which may reveal very rare symptoms that did not appear previously. This highlights the importance of "Post-Marketing Surveillance" as an additional safeguard for your health.
How do you contribute to enhancing drug safety?
Ibn Al-Haytham allows physicians, pharmacists, and consumers to report any side effects or product quality issues. Your report is more than just information; it is a vital step in enhancing drug safety and protecting other patients.
Direct Communication Channels:
You can send your reports through electronic form: Click here to fill out the reporting form.
Data Privacy and Information Security
Ibn Al-Haytham is committed to the highest levels of confidentiality and privacy. All information contained in reports, including the identity of the patient and the reporter, is treated as strictly protected data and will not be disclosed to any unauthorized party under any circumstances. It is used exclusively for evaluating pharmaceutical safety.
Note: Filling out the form may take a few minutes, but your contribution is the cornerstone of the journey to develop healthcare and ensure a safer future for all.
Frequently Asked Questions (FAQ) about Pharmacovigilance
We receive reports from everyone; whether you are a patient, a patient's relative, a doctor, or a pharmacist. Everyone's contribution is essential for building an accurate database regarding drug safety.
To ensure effective follow-up, it is preferable to provide four basic elements:
• A description of the side effect.
• The product name (preferably mentioning the Batch Number if available).
• Patient data (initials, age, or gender).
• Contact information of the reporter to follow up on the case.
The goal of the Pharmacovigilance department is to collect data to improve product safety in general. You must always consult your treating physician before making any decision to stop the medication or change its dose.
Our specialized team analyzes the data clinically, compares it with global studies, and takes preventive measures (such as updating the internal leaflet) to ensure the protection of other patients.
Absolutely not. Ibn Al-Haytham adheres to strict data protection protocols. Reports are processed for scientific and regulatory purposes only, without disclosing the personal identity of any individual.
| Taking 5 minutes to report a side effect could save another patient's life. Thank you for being our partner in drug safety. |