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Reporting by Healthcare Professional

  If you think you may be experiencing an adverse event caused by a medicine or medical device, seek advice from your doctor / pharmacist as soon as possible.

 


 

Reporting Adverse Drug Reactions

  • Please report ALL suspected Adverse Drug Reactions (ADRs) to the National Centre for Adverse Drug Reactions Monitoring, including those for vaccines, cosmetics and traditional products.
  • Do not hesitate to report if some details are not known.
  • The identities of Reporter, Patient and Institution will remain confidential.

 DOWNLOAD ADR FORM [MANUAL - PDF]

 

Note: Online ADR reporting for Healthcare Professionals will be temporarily unavailable due to database upgrading (from 9/12/2015 until further notice). Please download the manual form and submit by post, email or fax.

Click here for more information.

 


 

Product Complaints

Registered Product Complaints (Related to Medicine) Form [PDF]

 


 

 

Guide for ADR Reporters 

  • Definitions
  • Checklist for ADR Reporters
  • Submitting samples for Laboratory Testing of Suspected Adulterated Products
  • VigiAccess: A public gateway to the WHO ADR Database
  • ADR Reports on AntiTB drugs

 

GUIDE FOR ADR REPORTERS [PDF]

 


 

Cutaneous Adverse Drug Reaction (ADR) Classification

 

Clinical Manifestation of Cutaneous ADR Glossary and Pictures of Clinical Manifestation of Cutaneous ADR

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