Catalog Number CHLORAPREP UNKNOWN |
Device Problems
Adverse Event Without Identified Device or Use Problem (2993); Insufficient Information (3190)
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Patient Problems
Unspecified Infection (1930); Reaction (2414)
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Event Date 10/05/2020 |
Event Type
Injury
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Manufacturer Narrative
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(b)(6) initial emdr submission.A follow up emdr will be submitted if additional information becomes available.(b)(4).
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Event Description
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It was stated the patient experienced a lower respiratory infection and various adverse reactions while using chloraprep.
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Manufacturer Narrative
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No additional information was provided by the canada vigilance.Propharma did reach out to obtain with no success.Should additional information be available in the future, the complaint will be re-opened and investigated.All complaints are reviewed during monthly quality/safety meetings.In addition, complaints are trended at monthly quality data analyst meetings and quarterly plant management review meetings.
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Event Description
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It was stated the patient experienced a lower respiratory infection and various adverse reactions while using chloraprep.
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Search Alerts/Recalls
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