Regulatory manufacturer report number: 1627487-2020-01787.It was reported the patient experienced bruising of the spinal cord due to a dural puncture.In turn, the patient reported symptoms of a spinal headache and left leg weakness.Ct scan confirmed bruising but no hematoma.As a result, the spinal headache was addressed in related manufacturer reference number: 1627487-2020-02059 and related manufacturer reference number: 1627487-2020-02058.Reportedly, the physician advised the left leg weakness is normal and expected to last sometime after a dural puncture has taken place.
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