Ventricular Tachycardia Clinical Trial
Official title:
Post-marketing Registration Study of Nifekalant Hydrochloride (NIF) Injection
Retrospective and Prospective single arm, observational study to evaluate efficacy and safety of NIF in the treatment of ventricular tachycardia and ventricular fibrillation. The information registration of the target population will be collected with the hospital HIS system or LIS system.
Subjects enrolled in the retrospective study may be enrolled in a prospective study if the
study drug is re-used, but in the end only the most-registered case of the subject would be
collected.
The recommended treatment plan for this study is from the usage and dosage of NIF. The
clinician can make appropriate adjustments to the specific usage and dosage according to the
patient's condition.
Load dose: Adults usually use 0.3mg/kg each time, under continuous ECG monitoring, the
injection should be completed within 5 minutes, and the maximum dose should not exceed 0.5
mg/kg.
Maintenance dose: After load injection, the adult routine dose is 0.4 mg/kg/h under
continuous ECG monitoring. The dosage could be appropriately increased or decreased according
to the patient's reaction, but the maximum dose should not exceed 0.8 mg/kg/h.
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