FDA records indicate that there are no current recalls for this drug.
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In-111 Dtpa Solution Recall
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Questions & Answers
Side Effects & Adverse Reactions
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Legal Issues
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Manufacturer Warnings
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FDA Labeling Changes
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Uses
In-111 DTPA is indicated for use in radionuclide cisternography
History
There is currently no drug history available for this drug.
Other Information
In-111 DTPA is supplied as a sterile, pyrogen-free, isotonic, aqueous solution that is buffered to pH 7 to 8. At calibration time, each milliliter contains 2.5 mCi of Pentetate Indium Disodium In-111 (no carrier-added) and sodium bicarbonate for pH adjustment.
Sources
In-111 Dtpa Solution Manufacturers
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Anazaohealth Corporation
In-111 Dtpa Solution | Anazaohealth Corporation
Extreme care must be exercised to assure aseptic conditions in intrathecal injections. The maximum recommended intrathecal dose in the average patient (70kg) is 18.5 megabecquerels (500 microcuries). The patient dose should be measured by a suitable radioactivity calibration system immediately prior to administration. Parenteral drug preparations should be inspected visually for particulate matter and discoloration prior to administration whenever solution and container permit.
Storage and HandlingStore vial in its lead shield at a temperature of 5-30º C. Do not freeze
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