Rabeprazole belong to a group of medicines called Proton Pump Inhibitors (PPIs).Read More
Understand the benefits of using Rabeprazole and how Rabeloc will help you.Read More
Rabeloc is a prescription drug that should be used under your doctor’s guidance.Read More
Understand the Precautions and Warning Signs of Rabeprazole before using RabelocRead More
Understand the Side-effects of Rabeprazole before using RabelocRead More
ADVERSE EVENT REPORT
Understand how to report in case of possible side-effects from RabelocRead More
Rabeprazole belong to a group of medicines called Proton Pump Inhibitors (PPIs). Rabeprazole act by reducing the amount of acid made by the stomach.
Rabeloc is a prescription drug that should be used under your doctor’s guidance. Ensure you take the doctor’s advice before stopping to use the drug or changing its dosage.
Try not to skip the dose of Rabeprazole Sodium. However, if you missed the dose, take the medicine at the next dose, do not double the dose.
Do not overdose the drug for faster results. In case of overdose, seek medical attention immediately.
You must avoid using Rabeloc if you are:
It is advisable to talk to your doctor before taking Rabeloc or any Rabeprazole drug.
Doctors have prescribed Rabeloc to millions of patients to treat acid-related conditions safely over the years.
The safety of Rabeloc is already confirmed from many clinical trials with Rabeprazole in Tablet and injectable formulation. Since it is a Prescription drug, read package insert carefully before using. Inform your doctor/pharmacist of any side effects immediately &Keep away from children. For more information please contact your doctor.
As with any other drug, there can be side-effects of using Rabeloc. However, not many would experience the adverse effects of Rabeprazole.
The side effects experienced are usually mild but it may improve without stopping to take this medicine. Please consult your doctor and ask about possible side effects.
ADVERSE EVENT REPORT
Global Pharmacovigilance Department
The Global Pharmacovigilance department prioritize the patient safety by monitoring the safety of Cadila products. Pharmacovigilance is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other medicine/vaccine related problem. Global Pharmacovigilance takes an extensive approach to pharmacovigilance activities to establish, maintain, and communicate quality safety information throughout the life cycle of Cadila products.
In compliance with the applicable worldwide regulations, Cadila is committed to collect, review, and evaluate information regarding adverse events, product complaints, and other safety findings experienced by clinical trial subjects who receive our investigational drugs and by patients taking our approved products. This information helps us better understand, assess, and communicate the safety profile of Cadila products and allows us to deliver safer products to patients.
Adverse Event and Product Complaint Reporting
At Cadila Pharmaceuticals, we are committed to providing world-class medicines and understand the need for and importance of monitoring drug safety. It is Cadila's policy to comply with all regulations and laws worldwide relating to reporting adverse events, other safety finding and product complaints. Individuals are required to report adverse event, other safety finding and product complaint within one business day.
What information you need to report an Adverse Event
When reporting an adverse event, other safety finding or product complaint, you will need at to have the following information ready:
What to report:
Who can report:
Report even if:
How to report?
Contact patient safety at:
Sarkhej-Dholka Road, Bhat, Ahmedabad-382 210, INDIA.
Phone : +91-2718-251334
For detailed reporting click to download