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Factor VII Activity (1:5 dilution)

Coagulation

Factor VII activityFVIIProconvertin activity

Review status

Currently under review

Pending specialist review and validation.

What it shows

This test measures the activity of Factor VII, a clotting protein that helps start the clotting process when a blood vessel is injured. The result reflects how well your Factor VII works compared to normal clotting function. Laboratories perform the assay at a defined dilution to keep the measurement in an accurate range and to detect both decreases and increases in activity.

Factor VII is produced in the liver and depends on vitamin K. If Factor VII is too low or not working properly, you may bruise or bleed more easily. If it is higher than expected, it can be associated with a tendency to form clots in some situations.

Why it matters

Your clinician may order this test if you have unexplained bleeding, a prolonged prothrombin time, suspected inherited Factor VII deficiency, or conditions that affect vitamin K or the liver. It is also used to monitor the effects of vitamin K antagonists and to explore the cause of abnormal screening coagulation tests.

Understanding your Factor VII activity helps guide decisions about treatment, such as vitamin K replacement, adjusting anticoagulant medications, or further evaluation for liver or nutritional problems. In rare cases, it can help confirm a hereditary deficiency when bleeding symptoms or family history suggest it.

Understanding your results

A lower-than-expected activity can occur with inherited Factor VII deficiency, use of vitamin K antagonists, vitamin K deficiency from poor intake or malabsorption, severe liver disease, or widespread clotting activation. Certain antibiotics and other medicines can also reduce vitamin K–dependent clotting proteins. Your clinician will interpret the result alongside other tests, medications, diet, and medical history.

A higher-than-expected activity can be seen with acute inflammation, hormonal influences, or genetic variation. If your result is unexpected, your care team may repeat the test to rule out specimen issues, review medications and supplements, check related tests such as prothrombin time and liver function, or order specialized studies to confirm the cause. Most findings can be addressed with targeted steps, and urgent treatment is rarely needed unless you have active bleeding or clotting.

Reference ranges

0.51.5 U/mL
All sexes
0 days – 150 years

Reference intervals vary by laboratory, analyzer, methodology, population, and units. The ranges shown here are for education only. Always interpret your results against the reference interval printed on your own lab report.

Factors that could impact Factor VII Activity (1:5 dilution)

  • Citrate tube fill and handling

    Incorrect blood-to-anticoagulant ratio, high hematocrit, clots in the tube, or delayed processing can falsely lower or raise activity. Ensure the tube is filled to the mark and processed promptly.

  • Medications

    Vitamin K antagonists, some antibiotics, and high-dose salicylates can lower Factor VII activity. Tell your care team about all prescription drugs, over-the-counter products, and supplements.

  • Vitamin K and diet

    Poor intake, malabsorption, or recent changes in vitamin K consumption can reduce Factor VII activity. Consistent dietary patterns help stabilize vitamin K–dependent factors.

  • Liver function

    Factor VII is made in the liver. Hepatitis, cirrhosis, or acute liver injury can lower activity, often alongside changes in other clotting tests.

  • Physiologic states

    Acute illness, inflammation, pregnancy, and aging can influence Factor VII levels. Your clinician will consider these contexts when interpreting your result.

2026

References

  1. McGill University Health Centre. (2015, March 01). Factor VII 1:5 (Task CD 701493). Laboratory reference ranges.
  2. Clinical and Laboratory Standards Institute. (2004). Assays of coagulation factors; Approved guideline (CLSI document H51-A). Wayne, PA: CLSI.
  3. World Federation of Hemophilia. (2020). Diagnosis of hemophilia and other bleeding disorders: A laboratory manual (3rd ed.). Montreal, QC: WFH.