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. | – | Ravi Shankar et al.2010 |
How to report | Through completely filled yellow card form | – | Ravi Shankar et al.2010 |
Where it can be reported | Fully filled completely ADR form should be submitted to pharmacovigilance center | – | Palaian et al.2006 |