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Influenza A Viral Load Quantitative Test

DNA Labs India | ISO 9001:2015 Certified

Influenza A Viral Load Quantitative Test

Short Name: Influenza A Viral Load

Also known as: Influenza A PCR, Flu A Viral Load, Influenza A Quantitative PCR

Influenza A Viral Load Quantitative Test test available at DNA Labs India for ₹5,100. Uses Real Time PCR on Nasopharyngeal swab, throat swab, nasal swab, bronchial aspirate samples. Results in Reports are typically available by the 3rd working day after sample collection. Email reports are sent within 36 hours of result availability, and phone reporting is available within 24 hours.. Free home collection in 300+ cities across India.

Molecular🏠 Home Collection

🩺 Medically Reviewed By

Overview

The primary purpose of the Influenza A Viral Load Quantitative Test is to detect and measure the amount of Influenza A virus in a patient's respiratory sample. This test is used to confirm active infection, assess the severity of the disease, monitor the effectiveness of antiviral therapy, and guide clinical management. Unlike qualitative tests that only indicate presence or absence, the quantitative result helps clinicians determine the viral burden, which correlates with disease severity and infectivity. This is particularly important for patients who are critically ill, immunocompromised, or those who do not respond to initial treatment. Additionally, the test can be used for epidemiological surveillance and outbreak investigations. By providing a numerical viral load, the test enables healthcare providers to make informed decisions about hospitalization, isolation, and the use of antiviral medications such as oseltamivir. It also aids in differentiating Influenza A from other respiratory infections with similar symptoms, ensuring appropriate and timely treatment.

Test Code
6163
CPT Code
87502
ICD Code
J10.1
Price
₹5,100
Sample Type
Nasopharyngeal swab, throat swab, nasal swab, bronchial aspirate
Result Time
Reports are typically available by the 3rd working day after sample collection. Email reports are sent within 36 hours of result availability, and phone reporting is available within 24 hours.
Fasting Required
No
Method
Real Time PCR
Step 1

Sample Collection

No special preparation is required. Patients should inform their healthcare provider about any medications they are taking, especially antiviral drugs. A consent form must be signed before sample collection.

Method: Swab or aspirate

Step 2

Laboratory Analysis

The sample is collected by inserting a sterile swab into the nostril or throat, or by aspirating respiratory secretions. The procedure may cause mild discomfort but is generally well-tolerated.

Step 3

Report Delivery

No specific aftercare is required. Patients can resume normal activities immediately. The sample is sent to the laboratory for analysis.

Timeline: Reports are typically available by the 3rd working day after sample collection. Email reports are sent within 36 hours of result availability, and phone reporting is available within 24 hours.

Patient Instructions

1
Before the Test:No special preparation is required. Inform your doctor about any antiviral medications you are taking, as they may affect the viral load.
2
During the Test:The sample collection involves a swab from the nose or throat, which may cause mild discomfort but is quick and safe.
3
After the Test:You can resume normal activities immediately. The sample will be processed, and results will be available in 3 working days.

About This Test

Who Should Get This Test

The primary purpose of the Influenza A Viral Load Quantitative Test is to detect and measure the amount of Influenza A virus in a patient's respiratory sample. This test is used to confirm active infection, assess the severity of the disease, monitor the effectiveness of antiviral therapy, and guide clinical management. Unlike qualitative tests that only indicate presence or absence, the quantitative result helps clinicians determine the viral burden, which correlates with disease severity and infectivity. This is particularly important for patients who are critically ill, immunocompromised, or those who do not respond to initial treatment. Additionally, the test can be used for epidemiological surveillance and outbreak investigations. By providing a numerical viral load, the test enables healthcare providers to make informed decisions about hospitalization, isolation, and the use of antiviral medications such as oseltamivir. It also aids in differentiating Influenza A from other respiratory infections with similar symptoms, ensuring appropriate and timely treatment.

How to Prepare

  • Use a flocked swab for nasopharyngeal collection.
  • Insert the swab into the nostril parallel to the palate and leave in place for a few seconds to absorb secretions.
  • Place the swab into a viral transport medium tube and break the shaft at the scored line.
  • Label the tube with patient identification and collection date/time.
  • Transport the sample to the laboratory at 2-8°C or frozen if delayed.

Doctor's Notes

Reviewed by — MBBS, MD (Microbiology) · Reg. No. 27670

"Quantitative viral load testing is essential for monitoring severe influenza A infections, especially in immunocompromised patients, to guide antiviral therapy and assess treatment response."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeNasopharyngeal swab, throat swab, nasal swab, bronchial aspirate
Sample Volume1 swab or aspirate
ContainerViral transport medium (VTM) tube
Collection MethodSwab or aspirate

Sample Stability

Room temperature (20-25°C)Up to 48 hours
Refrigerated (2-8°C)Up to 72 hours
Frozen (-20°C or lower)Up to 7 days
Sample Rejection Criteria:
  • Sample not collected in appropriate viral transport medium.
  • Sample with insufficient quantity or poor quality (e.g., no epithelial cells).
  • Sample leaking or damaged during transport.
  • Sample not labeled correctly or missing patient information.
  • Sample received after prolonged delay without proper storage.

Understanding Your Results

The Influenza A Viral Load Quantitative Test provides a numerical value indicating the amount of viral RNA in the sample. Interpretation should be done by a qualified healthcare professional in the context of the patient's clinical presentation and medical history.
📊

Not detected

No Influenza A virus RNA was found. This suggests no active infection, but clinical correlation is needed as false negatives can occur.

📊

Detected (low viral load, e.g., <10,000 copies/mL)

Indicates active infection with low viral burden. May be seen in early or resolving infection. Antiviral therapy may still be considered based on symptoms.

📊

Detected (moderate viral load, e.g., 10,000-100,000 copies/mL)

Active infection with moderate viral load. Likely to be associated with significant symptoms. Antiviral treatment is recommended, especially in high-risk patients.

📊

Detected (high viral load, e.g., >100,000 copies/mL)

High viral burden indicates severe infection. Patients may require hospitalization and aggressive antiviral therapy. Close monitoring is essential.

⚠️ When to Consult a Doctor:

Consult a healthcare provider immediately if you experience severe symptoms such as difficulty breathing, chest pain, confusion, persistent high fever, or if symptoms worsen after initial improvement. Early medical consultation is crucial for high-risk individuals.

Limitations

  • A negative result does not completely rule out Influenza A infection, especially if the sample was collected late in the course of illness or if the viral load is below the detection limit.
  • The test detects Influenza A but does not differentiate subtypes (e.g., H1N1, H3N2) unless additional testing is performed.
  • Viral load may not directly correlate with disease severity in all patients, as host immune response also plays a role.
  • Results should be interpreted in conjunction with clinical findings and other laboratory tests.

Risks & Considerations

  • Mild discomfort during sample collection.
  • Slight risk of bleeding from the nasal passage if the swab is inserted too deeply (rare).
  • No significant systemic risks associated with the test.

Interfering Factors

  • Improper sample collection (e.g., inadequate swab) may lead to false negatives.
  • Sample degradation due to delayed transport or improper storage.
  • Presence of inhibitors in the sample (e.g., blood, mucus) that may affect PCR amplification.
  • Recent antiviral therapy may reduce viral load, leading to false low results.
  • Cross-contamination during sample processing.

Compare With Similar Tests

TestInfluenza A Viral Load Quantitative TestRapid Influenza Diagnostic Test (RIDT)Influenza A/B Qualitative PCRViral Culture
ComparisonInfluenza A Viral Load Quantitative Test

Frequently Asked Questions

What is the cost of the Influenza A Viral Load Quantitative Test?
The cost is INR 5100, which includes home sample collection and digital reports. The price may vary slightly based on location and any ongoing discounts.
How is the sample collected for this test?
A healthcare professional will collect a swab from your nasopharynx (back of the nose) or throat. In some cases, a bronchial aspirate may be collected for severe respiratory infections.
Do I need to fast before the test?
No, fasting is not required for this test. You can eat and drink normally before sample collection.
How long does it take to get the results?
Results are typically available by the 3rd working day after sample collection. You will receive an email within 36 hours of result availability, and phone reporting is available within 24 hours.
What does a 'detected' result mean?
A 'detected' result means that Influenza A virus RNA was found in your sample. The viral load value indicates the amount of virus, which helps assess severity and guide treatment.
Can this test differentiate between Influenza A subtypes like H1N1?
No, this test detects Influenza A generally. Subtyping requires additional tests, which may be ordered if clinically necessary.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection for this test in over 200 cities across India. You can book online and a trained phlebotomist will visit you.
What is the difference between this test and a rapid flu test?
Rapid flu tests provide results in 15 minutes but have lower accuracy and do not give a viral load. The quantitative PCR test is more sensitive and provides a numerical viral load, which is more informative for clinical management.
Who should get this test?
It is recommended for individuals with flu-like symptoms, especially those at high risk of complications (elderly, pregnant, immunocompromised), hospitalized patients, and for monitoring antiviral therapy.
Are there any risks associated with the test?
The test is safe. You may experience mild discomfort during the swab collection, but there are no significant risks.
Can I take antiviral medication before the test?
Yes, but inform your doctor, as antiviral drugs may reduce the viral load and affect the test results. The test can still be performed, but interpretation should consider this.
Is the test covered by insurance?
Insurance coverage varies. It is recommended to check with your insurance provider. DNA Labs India also offers affordable self-pay options.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

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Your Data Privacy

Your medical data is protected under Indian law.

Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.

DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.

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