Source: Medicines & Healthcare Products Regulatory Agency (GB) Revision Year: 2018 Publisher: Piramal Critical Care Limited, Suite 4, Ground Floor, Heathrow Boulevard East Wing, 280 Bath Road, West Drayton, UB7 0DQ, United Kingdom, Tel: 00441670562400
Hypnomidate is an intravenous induction agent of anaesthesia.
For intravenous administration.
Hypnomidate should be injected slowly by the intravenous route.
The product must only be used by physicians trained in endotracheal intubation. Equipment for artificial respiration must be available.
It is recommended to wear gloves while opening the ampoule. In the case of any accidental dermal exposure, rinse the affected area with water. Avoid use of soap, alcohol and other cleaning materials that may cause chemical or physical abrasions to the skin.
A dose of 0.3 mg/kg bodyweight given intravenously at induction of anaesthesia, gives sleep lasting from 4 to 5 minutes.
Dosage should be adjusted to the individual patient response and to clinical effects.
In children under 15 years the dosage may need to be increased: a supplementary dose of up to 30% of the normal dose for adults is sometimes necessary to obtain the same depth and duration of sleep as obtained in adults.
A dose of 0.15-0.2 mg/kg bodyweight should be given and the dose should be further adjusted according to the individual patient response and to clinical effects (see Section 4.4 Special Warnings and Precautions for Use).
Since Hypnomidate has no analgesic action, appropriate analgesics should be used in procedures involving painful stimuli.
Hypnosis can be prolonged by additional injections of Hypnomidate.
Do not exceed a total dose of 30 ml (3 ampoules).
Hypnomidate may be diluted with sodium chloride infusion BP or dextrose infusion BP but it is not compatible with compound sodium lactate infusion BP (Hartmann’s solution). Combinations with pancuronium bromide may show a very slight opalescence; for this reason the two should not be mixed together.
Overdosing is likely to result in prolonged anaesthesia with the possibility of respiratory depression and even arrest, in which case adequate respiratory support is mandatory. Hypotension has also been observed. Overdosage may depress cortical secretion. This may be associated with disorientation and delayed awakening.
General supportive measures and close observation are recommended. In addition, administration of 50-100 mg hydrocortisone (not ACTH) may be required for depression of cortisol secretion.
Shelf life: 2 years.
Do not store above 25°C.
Colourless glass ampoule, Ph.Eur. Type I, containing 10 ml Hypnomidate, in packs of 5 and 10 ampoules.
Not all pack sizes may be marketed.
None stated.
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