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MEDICINE SIDE EFFECT REPORTING FORM FOR CONSUMER INITIALREPORT:2nd EDITION 22/07/2020FOLLOWUPREPORT COMPLETION DD/MM/YYY. PATIENT DETAILS WHO EXPERIENCED THE SUSPECTED SIDE EFFECT(S)? YOU PATIENT
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How to fill out side effect reporting form

01
Start by downloading the side effect reporting form from the official website of the regulatory authority or pharmaceutical company.
02
Fill in your personal information accurately, including your name, contact details, and any relevant identification numbers.
03
Provide details about the medication or medical product that you experienced the side effects from, such as the brand name, batch number, and dosage.
04
Describe the specific side effect(s) you have experienced in as much detail as possible, including the onset, duration, and severity.
05
Indicate any other medications or medical conditions you have, as they may be relevant to the side effects experienced.
06
If you sought medical attention for the side effects, provide the name and contact information of the healthcare professional or facility.
07
Attach any supporting documentation, such as medical reports or test results, if available.
08
Review the completed form for accuracy and completeness.
09
Submit the side effect reporting form according to the instructions provided, either online or through mail.

Who needs side effect reporting form?

01
Anyone who has experienced side effects from a medication or medical product needs to fill out the side effect reporting form. This includes patients, healthcare professionals, and caregivers.
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Side effect reporting form is a document used to report any adverse reactions or unexpected side effects of a medication or medical device.
Healthcare professionals, patients, and manufacturers are required to file side effect reporting form.
Side effect reporting form can be filled out by providing detailed information about the adverse reaction, including when it occurred, the severity, and any actions taken.
The purpose of side effect reporting form is to collect data on adverse reactions to medications and medical devices in order to improve patient safety.
Information such as the patient's demographics, the medication or device involved, the reported side effect, and any relevant medical history must be reported on side effect reporting form.
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