Adverse Drug Reaction (ADR) Reporting
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1.What is an adverse reaction?
An adverse drug reaction (ADR) refers to a noxious response to an approved drug that occurs at normal doses during proper use and is not related to the drug’s intended therapeutic purpose. An ADR is not equivalent to a quality issue with the drug.
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2.Why are adverse events being reported?
GenSci has established multiple channels to continuously monitor the safety of our products. By reporting adverse events/reactions related to GenSci products, you contribute to our ongoing effort to refine our product safety features and ensure patient medication safety.
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3.How to report an adverse event?
If you experience an adverse event, you should consult a doctor promptly. Please complete the adverse event/reaction reporting form and you may also report adverse events/reactions by calling the hotline provided in the package insert. Thank you for reporting the adverse events/reactions! We wish you and your family good health!
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4.Privacy Statement
GenSci will adhere to privacy laws and ensure the confidentiality of you and the information you provide. Please be rest assured when providing your information!

Name*
Gender*
Date of Birth*
Prescription Hospital*
Reason for Medication*
Suspected Drug*
Drug Marketing Authorization Holder*
Batch Number/Strength*
Reporter*
Reporter Contact Information*
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Doctor
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Pharmacist
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Patient/Patient’s Family
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Nurse
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Other
Verification Code*
I have read and agree to GenSci’s Privacy Policy
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