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Rotapharm

REPORT AN ADVERSE EVENT

We ask healthcare professionals and patients to report any adverse events associated with the prescription or use of our company’s medicinal products:

The development of adverse reactions;
Medical errors / [tooltips keyword=”medication errors” content=”Medication error: Any unintentional error by a healthcare professional, patient or consumer in prescribing, dispensing, dosing or administering/taking a medicinal product.”];
Detection/use of poor-quality and falsified medicinal products;
Use of medicinal products for unstudied and unauthorized indications ([tooltips keyword=”off-label use” content=”Off-label use: The intentional use of a medicinal product for a medical purpose that does not comply with the approved instructions for medical use.”]);
Acute and chronic poisonings;
Cases of death when using medicinal products;
[tooltips keyword=”abuse of medicinal products” content=”Abuse of a medicinal product: Persistent or single excessive use of a medicinal product that is accompanied by adverse physiological or psychological effects”];
Unfavourable interactions of medicinal products with chemicals, food products and other medicines;
Cases of lack of efficacy of a medicinal product.

“Notifications on pharmacovigilance and personal data protection”

“Pharmacovigilance notification”

Making Improvements in People’s Life Possible!​

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