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.
OR
DOWNLOAD ADR FORM [MANUAL - PDF]*
* to submit by post, email or fax.
Product Complaints
Registered Product Complaints (Related to Medicine) Form [PDF]
