PRESCRIBING INFORMATION OMNIPAQUE™ (iohexol)
Please refer to full national Summary of Product Characteristics (SPC) before prescribing. Indications and approvals may vary in different countries. Further information available on request.

PRESENTATION
Aqueous solution for injection containing iohexol, a non-ionic, monomeric, triiodinated X-ray contrast medium, and available in five strengths containing either 140 mg, 180 mg, 240 mg, 300 mg or 350 mg iodine per ml.

INDICATIONS
X-ray contrast medium for use in adults and children for urography, phlebography, i.v. DSA, CT, arteriography, cardioangiography and i.a. DSA. Myelography. For use in body cavities: Arthrography, ERP/ERCP, herniography, hysterosalpingography, sialography and use in the G-I tract.

DOSAGE AND ADMINISTRATIONS
Adults & children: Dosage varies depending on the type of examination, age, weight, cardiac output and general condition of patient and the technique used (see SPC and package leaflet).

CONTRAINDICATIONS Manifest thyrotoxicosis. History of serious reaction to OMNIPAQUE.

WARNINGS AND PRECAUTIONS
Allergy, asthma, or previous reactions to contrast media are risk factors for developing hypersensitivity reactions/anaphylactic reactions. Necessary drugs and equipment must be available for immediate treatment, should a serious reaction occur. It is advisable always to use an indwelling cannula or catheter for quick intravenous access throughout the entire X-ray procedure. After contrast medium administration the patient should be observed closely for at least 15 minutes, since the majority of serious side effects occur within this time. However, delayed reactions may occur. To prevent acute renal failure, special care should be exercised in patients with preexisting renal impairment, diabetes mellitus, paraproteinemias (myelomatosis and Waldenström's macroglobulinemia), dehydrated patients, or patients who receive concurrent treatment with nephrotoxic drugs. To prevent lactic acidosis in diabetic patients treated with metformin, administration of metformin should be discontinued at the time of administration of contrast medium and withheld for 48 hours and reinstituted only after renal function has been re-evaluated and found to be normal. (Refer to SPC). Patients with acute cerebral pathology, tumours or a history of epilepsy, alcoholics and drug addicts are predisposed to seizures. Adequate hydration should be assured. Young infants (age < 1 year) and especially neonates are susceptible to electrolyte disturbance and haemodynamic alterations. Patients with serious cardiac disease and pulmonary hypertension may develop haemodynamic changes or arrhythmias. Special care should be exercised in patients with hyperthyroidism. One should also be aware of the possibility of inducing transient hypothyroidism in premature infants receiving contrast media. Symptoms of myasthenia gravis may be aggravated. Extravasation of contrast media may on rare occasions give rise to local pain, and oedema, which usually recedes without sequelae. However, inflammation and even tissue necrosis have been seen. Elevating and cooling the affected site are recommended as routine measures. Surgical decompression may be necessary in cases of compartment syndrome. Following myelography the patient should rest with the head and thorax elevated by 20° for one hour. Thereafter he/she may ambulate carefully but bending down must be avoided. The head and thorax should be kept elevated for the first 6 hours if remaining in bed. Patients suspected of having a low seizure threshold should be observed during this period. Outpatients should not be completely alone for the first 24 hours. A few patients have experienced a temporary hearing loss or even deafness after myelography.

PREGNANCY AND LACTATION
The safety of OMNIPAQUE in human pregnancy has not been established (see SPC). Omnipaque should not be used in pregnancy unless considered essential. Breast feeding may continue normally.

UNDESIRABLE EFFECTS
All routes of administration: Hypersensitivity reactions with mild respiratory or cutaneous symptoms or anaphylactic reactions with more severe manifestations. Vagal reactions causing hypotension and bradycardia, headache. Abdominal discomfort/pain, nausea, vomiting or diarrhoea, transient metallic taste. Iodism or "iodide mumps" resulting in swelling and tenderness of the salivary glands. Feeling of warmth, fever, rigors, hypertension. Intravascular use (Intraarterial and Intravenous use) Neurological reactions, including seizures or transient motor or sensory disturbances. Cortical blindness. Serious cardiac complications, including cardiac arrest, arrhythmia, depressed cardiac function or signs of ischaemia. A transient increase in S-creatinine, followed by renal failure in rare occasions. Distal pain or heat sensation in peripheral angiography.Transient ischaemia after injection into coronary, cerebral or renal arteries. Post phlebographic thrombophlebitis or thrombosis. Arthralgia. Severe respiratory symptoms and signs (dyspnoea, bronchospasm, laryngospasm, non-cardiogenic pulmonary oedema), cough. Thyrotoxicosis, flushing, injection site reaction. Intrathecal use: Meningism or chemical meningitis. Photophobia. Transient blindness, motor or sensory dysfunction. Confusion. Paraesthesia. Seizures. EEG changes. Local pain, cramping and pain in the lower limbs, neck pain. Headache, nausea, vomiting or dizziness. Injection site reaction.

Use in Body Cavities Endoscopic Retrograde Cholangiopancreatography (ERCP): Elevation of amylase levels, pancreatitis.
Oral use: Gastrointestinal upset. Hysterosalpingography (HSG): Transient pain in the lower abdomen. Arthrography: Post procedural pain. Frank arthritis. Herniography: Mild postprocedural pain.

INSTRUCTIONS FOR USE AND HANDLING
Like all parenteral products, OMNIPAQUE should be inspected visually for particulate contamination, discolouration and the integrity of the container prior to use. The product should be drawn into the syringe immediately before use. Containers are intended for single use only, any unused portions must be discarded. OMNIPAQUE may be warmed to body temperature (37°C) before administration.

MARKETING AUTHORISATION HOLDER
GE Healthcare AS
Nycoveien 1-2
P.O. Box 4220 Nydalen
N-0401 Oslo
Norway

CLASSIFICATION FOR SUPPLY
Subject to medical prescription (POM).

MARKETING AUTHORISATION NUMBER
PL PL 00637/0034-0038.

DATE OF REVISION OF TEXT
15 February 2007.

PRICE: 350 mgI/ml, 10 x 50 ml: £208.01.

Information about adverse event reporting can be found at www.yellowcard.gov.uk. Adverse events should also be reported to GE Healthcare.

www.gehealthcare.com