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Report an Adverse Drug Reaction (ADR)


At IntraHub Africa, patient safety is our highest priority. We are committed to supporting NAFDAC’s mission to strengthen pharmacovigilance and promote medicine safety across Nigeria. Through our dedicated ADR reporting system, we actively contribute to national safety monitoring efforts by collecting, assessing, and submitting adverse drug reaction (ADR) reports directly to NAFDAC in a timely and compliant manner.

Submit a Report

Please complete the form below to report an adverse drug reaction.  

Why Your Report Matters

Every report helps build safer healthcare systems by:

  • Identifying previously unrecognized side effects
  • Strengthening the safety profile of medicines in real-world use
  • Supporting NAFDAC’s regulatory decisions and risk minimization measures
  • Preventing harm to future patients

Who Can Report?

This form is open to:

  • Healthcare professionals (doctors, pharmacists, nurses, etc.)
  • ​Patients and caregivers
  • General public

What Information Should You Provide?

To ensure your report is processed efficiently, please include:

  • A description of the reaction (what happened, when, how severe)
  • The name of the suspected medicine (including strength and dose)
  • Basic patient details (age, gender, and initials only — no full names)
  • Any known medical history or allergies
  • Your contact information (optional, but helps us if follow-up is needed)

Confidentiality and Data Use

Your information is treated with the strictest confidentiality. We only use this data for regulatory reporting to NAFDAC and internal pharmacovigilance review, in accordance with ethical and legal standards