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Healthcare professional such as doctors, dentists, pharmacists and nurses are encouraged to report suspected adverse events encountered in their day to day practice.

Using the ADR google form given by the following link here, you can report Adverse Events.

Address
Director General / CEO
National Medicines Regulatory Authority,
No: 120, Norris Canal Road,
Colombo 10.
Telephone
+94 112 698 896, +94 112 698 897
Fax
+94 112 689 704

A copy of the form shall be forwarded to Adverse Drug Reaction Monitoring Unit of the Department of Pharmacology, Faculty of Medicine, University of Colombo, Kynsey Road, Colombo 08. (TP/ Fax: +94 112 697 483).

Importance of Reporting Adverse Events

When a new chemical entity (NCE) is first marketed, it would have been tested only in a limited number of patients/volunteers. Rare adverse drug reactions/events could be identified only after the drug is marketed and used by a much larger population. Safety information in use in special groups such as children, elderly, pregnant women etc. are not often available at the time of first marketing of a new drug.

120, Norris Canal Road, Colombo 10
 011-2687743
 info@nmra.gov.lk
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Last Update:
18 June 2024.