Generic drug of the therapeutic class: Anesthesia, resuscitation, analgesics
Active Ingredients: Ferrous Gluconate (E579), Copper Gluconate, Manganese Gluconate, Zinc Gluconate, Sodium Fluoride, Cobalt Gluconate, Sodium Iodide, Sodium Selenite, Ammonium Molybdate, Chromium Chloride
Solution for solution for IV infusion
Box of 25 bottles of 40 ml
DECAN is used as part of an intravenous nutritional protocol to cover basic needs or moderately increased trace elements during parenteral nutrition.
Dosage DECAN Concentrate for infusion IV Box of 25 vials of 40 ml
Reserved for adults.
The recommended daily dosage in patients with basic or moderately increased needs is one vial (40 ml).
In the event of significantly increased requirements for trace elements (for example in the case of extensive burns and in severely traumatized patients with significant hypercatabolism), the daily dosage may be of 2 bottles (80 ml) and a control of the blood level of oligo - Items is recommended.
DECAN is not intended to be administered as is.
DECAN can also be added as such in parenteral nutrition mixtures. In this case, carefully check the compatibility. Refer to the sections Incompatibilities and Special precautions for disposal and handling for incompatibilities and instructions for use.
Children or patients under 40 kg.
Pronounced cholestasis (blood level of bilirubin> 140 μmol / l)
Do not administer:
· Patients with known hypersensitivity to any of the active ingredients or the excipient.
· In case of Wilson's disease and haemochromatosis or if the blood level of any of the constituents of DECAN is high.
Decan side effects
The following side effect has been reported spontaneously after the product has been marketed. The frequency could not be estimated from the available data.
Organ System Class (SOC)
General disorders and conditions at the administration site
Pain at the administration site