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Ultratard (insulin human) - A10AE01

Updated on site: 10-Oct-2017

Isem tal-MediċinaUltratard
Kodiċi ATCA10AE01
Sustanzainsulin human
ManifatturNovo Nordisk A/S

ULTRATARD

EPAR summary for the public

This document is a summary of the European Public Assessment Report (EPAR). It explains how the Committee for Medicinal products for Human Use (CHMP) assessed the studies performed, to reach their recommendations on how to use the medicine.

What is Ultratard?

Ultratard is an insulin suspension for injection. Ultratard is supplied as 40 or 100 IU strengths in vials. Ultratard contains the active ingredient insulin human (rDNA).

Ultratard is used in patients with diabetes mellitus. Ultratard can be used in type 1 diabetes, when the pancreas cannot produce insulin, and in type 2 diabetes, when the body is not able to use insulin

effectively.

Product

The medicine can only be obtained with a prescription.

How is Ultratard used?

Ultratard is given subcutaneously (under the skin) by injection, usually in the thigh. If convenient it may also be given in the abdominal wall (tummy), the buttocks or the deltoid region (shoulder). The patient's blood sugar should be tested regularly to find the lowest effective dose. In type 1 diabetes, the dosage varies between 0.5 and 1.0 IU/kg (0.7 and 1.0 IU/kg in children before puberty), in type 2 diabetes the dosage is 0.3 to 0.6 IU/kg. Ultratard is a long-acting insulin, it can be given as a once daily or twice daily injection, with or without a fast-acting insulin (at meal times), according to the doctor’s recommendation.

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