Inclusion Criteria:

1. Patients with a tumorous lesion in the liver observed in diagnostic imaging such as
ultrasonography, etc., conducted between 1 and 35 days before administration of the
investigational agent, who are scheduled to undergo a dynamic CT examination.

2. Patients between 20 and 80 years old at the time informed consent is obtained.

3. Patients weighing >= 55.6 and < 105.0 kg at the time consent is obtained and when the
investigational agent is administered.

Exclusion Criteria:Issues affecting the safety evaluation of the investigational agent:

1. Patients who will have undergone or are scheduled to undergo an examination using
another contrast agent from 7 days before administration of the investigational agent
up to the time follow-up examinations are performed on day 8 after administration.

2. Patients for whom there is a strong possibility that a follow-up period, which
extends up until examinations are performed on day 8 after administration, would not
be possible, (i.e., when it will not be possible to evaluate delayed adverse drug
reactions).

3. Patients who have undergone or are scheduled to undergo surgical treatment or a
therapy such as percutaneous ethanol injection therapy, percutaneous microwave
coagulation therapy, radiofrequency ablation, or transcatheter arterial embolization,
etc., from the time diagnostic imaging such as abdominal ultrasonography is performed
up until follow-up examinations are conducted on day 8 after administration.

4. Patients who are unable to discontinue taking analgesics during the period from the
morning when the investigational agent is administered until CT examinations are
completed.

5. Patients who cannot stop taking biguanide antidiabetic drugs, such as metformin
hydrochloride and buformin hydrochloride, for three days after study agent
administration (including administration day).

6. Patients who are currently participating in another clinical study.

7. Patients who participated in another clinical study within the 6 months prior to
providing informed consent to participate in this study.

General concerns relating to the safety of the subject:

1. Patients in the acute stage of illness with unstable symptoms, or patients in a
life-threatening condition (when it is expected that emergency treatment may be
required between the time of registration and the conclusion of the follow-up period,
or when the patient is not expected to survive for 3 months following administration
of the investigational agent, etc.)

2. Patients with a history of hypersensitivity to iodine or iodinated contrast agents.

3. Patients with serious thyroid disease (goiter, hyperthyroidism, etc.)

4. Patients with serious cardiopathy (New York Heart Association [NYHA] functional class
IV heart failure, shock, cyanosis, peripheral circulatory insufficiency, ventricular
tachycardia, ventricular fibrillation, or complete atrioventricular block)

5. Patients with serious hepatopathy [symptoms of liver failure (fulminant hepatitis)
such as a disturbance of consciousness corresponding to grade 3 in the Criteria for
Grading Adverse Drug Reactions of Medicinal Products.]

6. Patients with moderate serious nephropathy (acute kidney failure, chronic kidney
failure, hydronephrosis, nephrotic syndrome, or uremia with serum creatinine levels
of 2.0 mg/dL or more, corresponding to grade 2 or above in the Criteria for Grading
Adverse Drug Reactions of Medicinal Products.)

7. Patients with bronchial asthma

8. Patients with acute pancreatitis

9. Patients with macroglobulinemia

10. Patients with multiple myeloma

11. Patients with tetany

12. Patients with pheochromocytoma or who are suspected of having pheochromocytoma

13. Pregnant and potentially pregnant women, and nursing mothers

14. Patients with a history of medicine hypersensitivity

15. Patients with serious myasthenia gravis

16. Patients judged by an investigator for any other reason to be ineligible for
participation as a subject in this study.