Type of investigation code: the filler was injected into the patient and is not accessible for return.The syringe was not returned for evaluation.Allergan is unable to confirm with the healthcare professional; therefore, additional event, product, or patient details are not attainable.The event is a physiological complication and analysis of the device generally does not assist allergan in determining a probable cause for this event.This is a known potential adverse event addressed in the product labeling.
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Healthcare professional (hcp) reported that a patient experienced "edema, induration, signs of vascular compression on the skin, pain in the chin area" after injection nine months ago in the subdermal and lips with juvéderm® volbella¿ with lidocaine, in the chin with [unspecified] juvéderm® voluma¿ and seven months ago in the lips with juvéderm® ultra smile.Treatment and symptom information not provided.This is the same event and the same patient reported under mdr id# 3005113652-2022-00728 (allergan complaint #(b)(4).This mdr is being submitted for the suspect product, [unspecified] juvéderm® voluma¿.
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