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Safety Data Sheet according to Regulation (EC) No. 1907/2006 (REACH) according to Regulation (EU) No. 2020/878 Trade name :102712 Calcium Dgluconate monohydrate, USPRevision date : Print date :04/11/2022
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01
Wash hands before handling the medication.
02
Check the expiration date on the medication.
03
Follow the dosage instructions provided by your healthcare provider.
04
Dilute the calcium d-gluconate as directed before administration.
05
Administer the medication slowly through a vein, as instructed by a healthcare professional.
06
Monitor the patient for any signs of adverse reactions during and after administration.

Who needs 102712 - calcium d-gluconate?

01
Patients with hypocalcemia (low calcium levels in the blood)
02
Patients with conditions that require intravenous calcium supplementation, such as hypoparathyroidism or osteoporosis
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102712 - calcium d-gluconate refers to a specific regulatory filing related to the reporting of this pharmaceutical compound, which is used in various medical treatments.
Manufacturers, distributors, and healthcare providers who handle calcium d-gluconate are required to file the 102712 form to comply with regulatory requirements.
To fill out the 102712 form, you need to gather all necessary information regarding the product, including its composition, intended use, and distribution details, and then enter that information accurately into the provided fields on the form.
The purpose of 102712 - calcium d-gluconate is to ensure that regulatory authorities have accurate and timely information about the production and distribution of this compound, which is important for public health monitoring.
The information that must be reported includes the product name, manufacturer details, concentration, batch numbers, expiration dates, and the intended use of the product.
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