Reporting by Healthcare Professional

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  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

 

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

 

 


 

 

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

 ONLINE REPORTING

 

User Guide for Online Reporting

Reminder! Please read this user guide before proceeding to complete the online reporting form.

 

OR

 DOWNLOAD ADR FORM [MANUAL - PDF]*

 * to submit by post, email or fax.

 


 

Product Complaints

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

 


 

National Pharmaceutical Regulatory Agency (NPRA)
Lot 36, Jalan Universiti, 46200 Petaling Jaya, Selangor, Malaysia.
  • Email: npra@npra.gov.my
  • Phone: +603-7883 5400
  • Fax: +603-7956 2924, +603-7956 7075

DISCLAIMER

The Government of Malaysia and the National Pharmaceutical Regulatory Agency are not responsible for any loss or damage caused by the usage of any information obtained from this website.

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  • Last Modified: Monday 17 December 2018, 11:54:20.
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