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Study Subject ID Mothers date of birth year month day Discontinuation of Study Medication Upon receipt of a written notice of discontinuation from the CC or a patients written request to discontinue
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How to fill out discontinuation of study medication:

01
Obtain the discontinuation form from the appropriate authority or department responsible for managing the study medication.
02
Fill out the required personal information such as name, age, contact details, and any other identifying information.
03
Indicate the reason for discontinuation of the study medication. This could be due to adverse effects, non-compliance, or any other valid reason.
04
Provide details about the specific study medication being discontinued, including the name, dosage, and frequency of administration.
05
If possible, include the date of initiation and duration of the study medication to provide context.
06
Sign and date the form to confirm your understanding and agreement with the discontinuation.
07
Submit the filled-out form to the appropriate authority or department as instructed.

Who needs discontinuation of study medication:

01
Participants in clinical trials who experience adverse effects or intolerable reactions to the study medication may require discontinuation.
02
Individuals who are non-compliant with the study medication regimen may also need to discontinue their participation.
03
In some cases, the study protocol may require discontinuation of certain medications or treatment due to changes in the study design or safety concerns.
04
Participants who experience significant improvement in their conditions or achieve the desired outcomes may no longer require the study medication and therefore need to discontinue it.
05
It is important to consult with the research team or medical professionals responsible for the study to determine if discontinuation is necessary and appropriate.
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Discontinuation of study medication is the process of stopping the administration of medication to participants in a research study.
The principal investigator or study coordinator is usually responsible for filing discontinuation of study medication.
Discontinuation of study medication is typically filled out by documenting the reason for discontinuation, participant information, and any relevant details.
The purpose is to ensure accurate tracking of medication administration and to report any issues or changes in the study.
Information such as the reason for discontinuation, participant ID, date of discontinuation, and any adverse events must be reported.
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