Catalog Number UNK JUVEDERM-CONC/ADD |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Cytomegalovirus (CMV) Infection (2220)
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Event Type
Injury
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Manufacturer Narrative
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Further information from the reporter regarding event, product, or patient details has been requested.No additional information is available at this time.The events are physiological complications and analysis of the device generally does not assist allergan in determining a probable cause for these events.The filler was injected into the patient and is not accessible for return.The syringe was not returned for evaluation.This is a known potential adverse event addressed in the product labeling.
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Event Description
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Patient reported that they were injected with an unspecified juvéderm® and experienced a ¿cold sore.".
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Event Description
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Patient reported that they were injected with an unspecified juvéderm® and experienced a ¿cold sore.".
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Manufacturer Narrative
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Additional, changed, and/or corrected data: b.7.
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Manufacturer Narrative
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This medwatch is being submitted to correct g.3.For the initial medwatch submitted on 23/aug/2021.The aware date is 06/may/2021, not 29/jul/2021.
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Event Description
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Patient reported that they were injected with an unspecified juvéderm® and experienced a ¿cold sore.".
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Search Alerts/Recalls
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