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Test Price

550 AED

✅ Home Collection Available

Influenza B RNA Detection (Qualitative) Test in UAE | 550 AED | DNA Labs UAE

Executive Summary & Core Metrics

Accuracy Guarantee: 99.9% diagnostic sensitivity via Real-Time PCR on nasopharyngeal swabs, processed under ISO 9001:2015 certified laboratory (Cert: INT/EGQ/2509DA/3139) with whole genome sequencing confirmation for equivocal results.
Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection available daily from 8 AM to 11 PM, ensuring sample stability and rapid turnaround.
Clinical Guidance: Complimentary telephonic post-test clinical interpretation by our medical team, facilitating immediate specialist referral when required.
Insurance: Direct billing verification via WhatsApp at +971 54 548 8731. Please provide your Emirates ID and policy card.

Test Overview & Methodology

This molecular assay detects Influenza B viral RNA with unparalleled precision, distinguishing acute infection from bacterial or Influenza A mimics. The test is mandatory for high-risk patients and aligns with UAE DHA respiratory panels. Using Real-Time PCR with locked nucleic acid probes, the assay can detect as few as 10 viral copies per reaction, delivering a 99.9% analytical sensitivity.

Feature Our Test (RT-qPCR) Rapid Antigen Test
Diagnostic Sensitivity 99.9% – detects as few as 10 viral copies/reaction 50–70%; may miss early or low viral load infections
Methodology Real-Time PCR with locked nucleic acid probes; supplementary WGS for typing Lateral flow immunoassay
Turnaround Time 24 hours (phone) / 36 hours (email) from lab receipt 15–30 minutes, but with high false negatives
Clinical Utility Confirms influenza B RNA; guides antivirals (oseltamivir) and isolation protocols Presumptive screening only; negative results require PCR confirmation

Physician Insight & Safety Protocols

“In my practice, accurate respiratory diagnostics are essential. This PCR test removes uncertainty; a positive result enables prompt antiviral therapy and infection control measures, while a negative result directs us to other treatable causes with equal urgency. Please share any recent travel, vaccination, or immune-suppressing conditions with your phlebotomist.”

— Dr. Ajay Singh, General Practitioner, DHA License No. 36234132.

Advisory: Medication Caution

⚠️ Do not discontinue any prescribed medication, including antivirals or inhalers, without consulting your attending physician. This test is for diagnosis only; treatment decisions require clinical correlation.

Exclusion Criteria & Emergency Red Flags

  • Exclusion: Inability to tolerate nasopharyngeal swab due to recent nasal surgery, craniofacial trauma, or severe coagulopathy; alternative throat swab may be considered.
  • Exclusion: Lack of signed informed consent or documented clinical history; testing cannot proceed without a guardian for minors as per UAE regulations.
  • Red Flag – Seek Emergency Care Immediately: Bluish lips or face (cyanosis), severe difficulty breathing, confusion, or unresponsiveness, regardless of test result.
  • Red Flag: Fever >39.5°C persisting >72 hours despite antipyretics, or chest pain with each breath; do not wait for home collection results.

Patient FAQ & Clinical Guidance

1. How accurate is the Influenza B RNA detection test compared to a rapid kit?

This RT-qPCR delivers 99.9% analytical sensitivity, making it the gold standard for confirming active influenza B infection. Unlike antigen tests, it amplifies viral RNA, eliminating false negatives even when symptoms are mild or viral load is low.

2. When will I receive my results, and how are they communicated?

We provide a phone notification within 24 hours of sample receipt and a detailed email report by the 3rd working day, including your viral load interpretation. You will also receive a secure PDF highlighting your LOINC code 34487-9 for insurance claims.

3. Do I need to fast or stop medications before the nasal swab?

No fasting is required; the nasopharyngeal swab collection is unaffected by food or drink. Continue all prescribed medications, but inform your phlebotomist about any anticoagulant use or recent nasal sprays.

UAE Regulatory & Data Privacy Adherence

Data Protection: DNA Labs UAE operates in full compliance with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. All patient data is encrypted in transit and at rest, with access strictly limited to authorized clinical personnel.

Clinical Safety: The laboratory follows safety and consent guidelines under Federal Decree-Law No. 4 of 2016 on Medical Liability, ensuring every test is performed with informed consent and adherence to the highest standards of care.

Clinical & Logistical Metadata

Test Name Influenza B RNA Detection (Qualitative) by Real-Time PCR
Price (AED) 550
Turnaround Time 24 hours (phone notification) / 36 hours (email report)
Sample Type / Matrix Nasopharyngeal swab (or throat swab if contraindicated)
Methodology Used Real-Time PCR (RT-qPCR) with locked nucleic acid probes; supplementary whole genome sequencing for equivocal results
ICD-10-CM Code J10.1 (Influenza due to other identified influenza virus with other respiratory manifestations)
LOINC Code 34487-9 (Influenza virus B RNA [Presence] in Specimen by NAA with probe detection)
DHA Facility License & Laboratory Address DNA Labs UAE – DHA License No. 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE

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