Skip to main content

Table 5 Knowledge of pharmacovigilance and ADR reporting among the participants (n = 450)

From: Assessment of pharmacovigilance activities among pharmacist interns in Nigeria: a cross-sectional study

Question

Yes

N (%)

No

N (%)

I don't Know

N (%)

Definition of pharmacovigilance

475 (99.4)

3 (0.6)

 

Definition of ADR

475 (99.4)

 

3 (0.6)

ADR and ADE are different

382 (79.9)

51 (10.7)

45 (9.4)

Yellow form is a tool for reporting ADR in Nigeria

365 (76.4)

5 (1.0)

108 (22.6)

Pharmacovigilance center, through NAFDAC, regulates ADR reporting in Nigeria

416 (87.0)

10 (2.1)

52 (10.9)

Classes of ADRs include (i) dose-related, (ii) allergic, and (iii) idiosyncratic

435 (91.0)

21 (4.4)

22 (4.6)

Most important purpose of PV is to ensure safety of drugs

456 (95.4)

8 (1.7)

14 (2.9)

All severe ADRs of drugs are known before a drug is marketed

238 (49.8)

227 (47.5)

13 (2.7)

ADRs previously documented by manufacturers need not be reported again

216 (45.2)

207 (43.3)

55 (11.5)

  1. ADR Adverse drug reaction, PV pharmacovigilance, NAFDAC National Agency for Food and Drug Administration Control