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ULTRAVIST 300 INJECTION 300 mg Iodine/ml

Prescription Only
Drug type: Therapeutic
ATC code: V08AB05
Dosage form: INJECTION
Route of administration: INTRAVENOUS, INTRAVASCULAR, INTRACAVITARY, INTRA-ARTERIAL
Active ingredient: IOPROMIDE EQV IODINE; IOPROMIDE EQV IODINE

4.1 Indications

This medicinal product is for diagnostic use only.

Ultravist 300:

Contrast enhancement in computerized tomography (CT), digital subtraction angiography (DSA), intravenous urography, phlebography of the extremities, venography, arteriography, visualization of body cavities (e.g. arthrography, hysterosalpingography, fistulography) with the exception of myelography, ventriculography, cisternography.

Ultravist 370:

Contrast enhancement in computerized tomography (CT), digital subtraction angiography (DSA), intravenous urography, arteriography and especially angiocardiography, visualization of body cavities (e.g. arthrography, fistulography) with the exception of myelography, ventriculography, cisternography.

4.3 Contraindications

There are no absolute contraindications to the use of Ultravist.

4.2 Dosage and method of administration

4.2.1 General information

Contrast media which are warmed to body temperature before administration are better tolerated and can be injected more easily because of reduced viscosity.

For additional instructions, see section ‘Instructions for use/handling’ – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information.

4.2.2 Dosage regimen

Intravenous urography

Adults

The dose should not be less than 1 ml Ultravist 300 (0.8 ml Ultravist 370)/kg body weight if the clinical problem also requires adequate filling of the ureters. Increasing the dose is possible if this is considered necessary in special indications.

Children

The physiologically poor concentrating ability of the still immature nephron of infantile kidneys demands relatively high doses of contrast medium, e.g. with the use of Ultravist 300:

Neonates: 1.2 g l/kg body weight, corresponding to 4.0 ml/kg body weight

Babies: 1.0 g l/kg body weight, corresponding to about 3.0 ml/kg body weight

Small children: 0.5 g l/kg body weight, corresponding to about 1.5 ml/kg body weight

Filming times

When the above dosage guidelines are observed and Ultravist 300/370 is injected over 1 to 2 minutes, the renal parenchyma is usually highly opacified 3 to 5 minutes and the renal pelvis with the urinary tract 8 to 15 minutes after the start of administration. The earlier time should be chosen for younger patients and the later time for older patients.

In babies and young children it is advisable to take the first film as early as about 2 minutes after the administration of the contrast medium. Insufficient contrast can necessitate later films.

Computerized tomography (CT)

Whole-body CT

In whole-body computerized tomography, the necessary doses of contrast medium and the rates of administration depend on the organs under investigation, the diagnostic problem and, in particular, the different scan and image reconstruction times of the scanners in use. The infusion should be preferred for slow scanners and the injection as a bolus for fast scanners.

Cranial CT

The following dosages are recommended for cranial CT:

Ultravist 300: 1.0 – max. 2.0 ml/kg body weight

Ultravist 370: 1.0 – max. 1.5 ml/kg body weight

Conventional Angiography

Recommended doses for single injections:

Cerebral angiographyAortic arch angiography50 – 80ml Ultravist 300Retrograde carotid Angiography30 – 40ml Ultravist 300Selective angiography6 – 15 ml Ultravist 300

Thoracic aortography

50 – 80 ml Ultravist 300

Abdominal aortography

40 – 60 ml Ultravist 300

Angiography of the extremitiesUpper extremities:Arteriography8 – 12 ml Ultravist 300 Venography15 – 30 ml Ultravist 300

Lower extremities:Arteriography20 – 30 ml Ultravist 300Venography30 – 60 ml Ultravist 300

Angiocardiography

Selective, in the individual cardiac cavities: 40 – 60ml Ultravist 370

Coronary angiography 5 – 8ml Ultravist 370

Intravenous Digital subtraction angiography (DSA)

The i.v. injection of 30 – 60 ml Ultravist 300 or 370 as a bolus (flow rate: 8 – 12 ml/second into the cubital vein; 10 – 20 ml/second into the vena cava) is only recommended for contrast demonstrations of great vessels of the trunc. The amount of contrast medium remaining in the veins can be reduced and diagnostically used by flushing with isotonic sodium chloride solution as a bolus immediately afterwards.

Adults: 30 – 60 ml Ultravist 300/370

4.2.3 Additional information on special populations

4.2.3.1 Newborns (< 1 month) and infants (1 month – 2 years)

Young infants (age <1 years) and especially newborns are susceptible to electrolyte imbalance and hemodynamic alterations. Care should be taken regarding the dose of contrast medium to be given, the technical performance of the radiological procedure and the patient status.

4.2.3.2 Patients with renal impairment

Since iopromide is excreted almost exclusively in an unchanged form via the kidneys, the elimination of iopromide is prolonged in patients with renal impairment. In order to reduce the risk of additional contrast media-induced kidney injury in patients with pre-existing renal impairment, the minimum possible dose should be used in these patients (see also sections ‘Special warnings and precautions for use’ and ‘Pharmacokinetic properties’ – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information).

Registrant
BAYER (SOUTH EAST ASIA) PTE LTD
Approval Date
1991-05-14
Approval Number
SIN05841P
Manufacturer
Bayer AG (Berlin, Müllerstraße)
Licence Holder
BAYER (SOUTH EAST ASIA) PTE LTD