At AQUA VITOE LABORATORIES, the safety of our patients and healthcare professionals (HCPs) is of the utmost importance. We are committed to ensuring that our products meet the highest standards of quality, efficacy, and safety. To maintain transparency and safeguard public health, we have developed a robust Pharmacovigilance system to monitor, assess, and respond to adverse events associated with our products.
What is Pharmacovigilance?
Pharmacovigilance (PV) refers to the science and activities related to detecting, assessing, understanding, and preventing adverse effects or any other drug-related problems. It plays a crucial role in ensuring that AQUA VITOE LABORATORIES products are safe for use by continuously monitoring and evaluating any reported issues.
Reporting Adverse Events
We encourage all healthcare professionals and patients to report any adverse events or side effects they may experience while using AQUA VITOE LABORATORIES products. Your reports contribute to improving the safety of medications and help us take immediate action to prevent further risks.
Who Can Report?
- Healthcare Professionals (Doctors, Nurses, Pharmacists, etc.)
- Patients and Caregivers
- Hospital Authorities
What to Report?
Please report any of the following related to AQUA VITOE LABORATORIES products:
- Side effects or unexpected adverse reactions
- Lack of expected drug efficacy
- Medication errors
- Drug interactions
- Any other unusual effects related to product use
How to Report an Adverse Event?
You can report any adverse events related to AQUA VITOE LABORATORIES products through the following methods:
1. Email
Send your report directly to our Pharmacovigilance department at pv@aquavitoelab.com Kindly include:
- Product name
- Batch number (if available)
- Description of the event
- Patient details (age, gender, etc.)
- Contact details (for follow-up if needed)
2. Contact Number
For immediate reporting or to speak to our Pharmacovigilance experts, call our toll-free number: 9216506354 and 6230162305.
3. Postal Mail
You can also mail us your adverse event report. Please send the details to the address below:
AQUA VITOE LABORATORIES
Pharmacovigilance Department
Plot No: 04, Village Kunjhal,Nr. Jharmajri,Baddi , Distt : Solan (H.P) 173205.
Why Your Report Matters
Your contribution is vital for improving drug safety and ensuring better outcomes for all patients. Every report helps us enhance our understanding of product safety profiles and take the necessary actions to protect public health.
For more detailed information about adverse drug reactions (ADRs) and to report ADRs using official forms, you can also visit the Pharmacovigilance Programme of India (PvPI) website. The PvPI provides access to downloadable ADR reporting forms for both healthcare professionals and patients.
Visit: https://www.ipc.gov.in/PvPI/adr.html
Together, let’s ensure patient safety and the continuous monitoring of medication effects for a safer healthcare system.