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This document is used for capturing patient information and details related to the randomization and administration of study drugs in a clinical trial focusing on magnesium therapy in coronary patients.
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How to fill out MAGIC: Magnesium in Coronaries Form 01 – Randomization & Study Drug Administration Form

01
Obtain a copy of the MAGIC: Magnesium in Coronaries Form 01.
02
Fill in the patient's identification details at the top of the form.
03
Document the patient's demographic information, including age, sex, and medical history.
04
Specify the details of the randomization process, including the assigned group or treatment.
05
Record the date and time of administration of the study drug.
06
Include any relevant baseline measurements or assessments required for the study.
07
Ensure all sections of the form are complete and legible.
08
Sign and date the form to confirm accuracy and compliance.
09
Submit the completed form to the appropriate study coordinator or database.

Who needs MAGIC: Magnesium in Coronaries Form 01 – Randomization & Study Drug Administration Form?

01
Researchers conducting the MAGIC study.
02
Clinical trial coordinators overseeing the administration of the study drug.
03
Healthcare professionals involved in the treatment of patients participating in the study.
04
Regulatory oversight personnel requiring documentation for compliance.
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People Also Ask about

Magnesium sulfate 10 mmol (2.5 g = 5 mL from ONE vial) diluted with 100 mL of sodium chloride 0.9%, administer by IV infusion over 20-60 minutes. Total volume: 105 mL. Maximum rate of infusion: 315 mL/hr.
Peripherally, magnesium produces vasodilatation with flushing and sweating at moderate doses and lower blood pressure at higher doses. Onset of action after intravenous administration is virtually immediate and lasts for approximately 30 minutes.
Magnesium sulfate is used for short-term relief of constipation. It is also used as a soaking solution to relieve minor sprains, bruises, muscle aches or discomfort, joint stiffness or soreness, and tired feet. This medicine is a laxative and soaking solution.
Indications Constipation. Hypomagnesemia. Prevention of seizures in eclampsia/preeclampsia. Acute nephritis (pediatric patients) Cardiac arrhythmias secondary to hypomagnesemia. Soaking minor cuts or bruises.
Magnesium sulfate administration can be oral (PO), intramuscular (IM), intraosseous (IO), or intravenous (IV). For every 1 gram of magnesium sulfate, it contains 98.6 mg or 8.12 Eq of elemental magnesium. Magnesium sulfate can be combined with dextrose 5% in water to make intravenous solutions.
What is this medication? MAGNESIUM SULFATE (mag NEE zee um SUL fate) prevents and treats low levels of magnesium in your body. It may also be used to prevent and treat seizures during pregnancy in people with high blood pressure disorders, such as preeclampsia or eclampsia.
Magnesium is most commonly used for constipation, as an antacid for heartburn, for low magnesium levels, for pregnancy complications called pre-eclampsia and eclampsia, and for a certain type of irregular heartbeat (torsades de pointes).

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MAGIC: Magnesium in Coronaries Form 01 is a document used to record the randomization and administration of magnesium treatment in clinical study participants, aimed at evaluating its effects on coronary conditions.
Clinical trial investigators and designated research staff are required to file the MAGIC: Magnesium in Coronaries Form 01 as part of the protocol for managing and documenting the study drug administration.
To fill out the MAGIC form, follow the guidelines provided in the study protocol, ensuring that all mandatory fields such as participant ID, randomization allocation, dosage, and administration details are accurately completed and signed by authorized personnel.
The purpose of the form is to maintain accurate records of participants' randomization to treatment groups and the details of study drug administration, ensuring adherence to the study protocol and facilitating data analysis.
The form must report information such as participant identification number, randomization group, date and time of drug administration, dosage, and any adverse reactions observed during the administration of the study drug.
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