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





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.



User Guide for Online Reporting

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




 * 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 (Jalan Prof Diraja Ungku Aziz), 46200 Petaling Jaya, Selangor, Malaysia.

  • Phone: +603-7883 5400



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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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Site Last Modified

  • Last Modified: Khamis 20 Jun 2024, 10:17:13.
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