• WHO-GMP, GLP & ISO Certified

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Complaint Box

Section 1: Basic Information

Section 2: Complaint Type (Select One)







Section 3: Product Details (if applicable)

Section 4: Please describe your issue or query in detail

Section 5: Attachments (Optional)

Section 6: Preferred Response Method


Adverse Drug Reaction (ADR) Reporting Form

At JPEE DRUGS, patient safety is our top priority. The Adverse Drug Reaction (ADR) Reporting Form has been created to collect information about any suspected side effects or reactions related to our pharmaceutical products. ADR reporting helps us continuously monitor the safety, quality, and effectiveness of our medicines. Information received through this form is carefully reviewed by our pharmacovigilance team and used to identify potential risks, improve product safety, and comply with regulatory requirements. We encourage healthcare professionals, patients, and caregivers to report any suspected ADRs, even if the reaction is mild or uncertain. All reports are kept strictly confidential and are used only for drug safety monitoring purposes.

(ADR) Reporting Form
jpeedrugs.com