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Table 5 Details required for reporting ADR events

From: Adverse drug reactions monitoring: prospects and impending challenges for pharmacovigilance

Elements in ADR reporting

Necessary information

Others

References

What should be reported

Adverse reactions of the drug, suspected drug’s details, patient’s information

Medications overdose, pharmaceutical defect, drug interactions

Goldman1998

Who can report

medical practitioners or health care professionals, doctors, nurses, pharmacists, assistants, pharmaceutical technicians, pharmaceutical assistants, clinical officers and other health care providers

Manufacturers, all government and private hospital’s health center

Palaian et al.2006

When it can be reported

Any adverse reactions if noticed should be reported as soon as possible.

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Ravi Shankar et al.2010

How to report

Through completely filled yellow card form

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Ravi Shankar et al.2010

Where it can be reported

Fully filled completely ADR form should be submitted to pharmacovigilance center

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Palaian et al.2006