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Test Price

600 AED

✅ Home Collection Available

Influenza Group A & B (RNA Detection) Qualitative Test in UAE | 600 AED | Molecular Gold Standard

Executive Summary & Core Metrics

Clinical Utility: This qualitative Real-Time PCR test is the recognized gold standard for diagnosing Influenza A and B, delivering 99.9% sensitivity and specificity for definitive viral RNA detection from a standard nasopharyngeal swab.

  • Diagnostic Sensitivity: 99.9%
  • Turnaround Time: 24 hours (phone) / 36 hours (email)
  • Home Collection: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain available daily from 8 AM to 11 PM
  • Insurance & Billing: Direct billing verification via WhatsApp +971 54 548 8731

Test Overview & Methodology

The assay utilizes Real-Time Polymerase Chain Reaction (qPCR) targeting highly conserved regions of the viral genome. This advanced molecular methodology allows for precise differentiation between Influenza A and Influenza B while delivering the highest possible diagnostic accuracy compared to rapid antigen tests.

Feature This Test (Real-Time PCR) Rapid Antigen Test
Precision 99.9% sensitivity & specificity ~70-80% sensitivity
Methodology Real-Time PCR (qPCR) with RNA detection Lateral flow immunoassay
Result Speed 24 hours (phone), 36 hours (email) 15 minutes

Physician Insight & Safety Protocols

"As a General Practitioner managing respiratory infections in the UAE, I rely on the definitive clarity of PCR testing. Knowing the exact viral etiology guides accurate treatment, isolation protocols, and reduces unnecessary antibiotic use. It is crucial to continue any prescribed medications and seek immediate care for severe symptoms like breathlessness or chest pain."

— Dr. Ajay Singh, DHA License: 36234132

Medication Advisory

Do not discontinue prescribed medication without consulting your treating physician.

Exclusion Criteria & Emergency Red Flags

Seek Emergency Care Immediately If You Experience:

  • Severe respiratory distress or difficulty breathing.
  • Altered consciousness, confusion, or cyanosis.
  • Severe dehydration or inability to tolerate oral fluids.
  • Immunocompromised status accompanied by high fever.

Patient FAQ & Clinical Guidance

1. What is the difference between this PCR test and a rapid antigen test?

Our Real-Time PCR test amplifies viral genetic material, providing 99.9% sensitivity. Rapid antigen tests detect surface proteins and are far less sensitive, often missing active infections, especially in individuals with mild symptoms or early-stage disease.

2. How should I prepare for the nasopharyngeal swab collection?

No special preparation is required. Please avoid using nasal sprays or decongestants for at least 30 minutes prior to collection to ensure an adequate sample. A signed consent form and a brief clinical history will be required before the procedure.

3. Can I take antiviral medication before the test?

Yes, you can. However, please inform our clinical team about any antivirals or other medications you are taking. While antiviral therapy may slightly reduce viral load, it typically does not cause a false negative result with high-sensitivity PCR testing.

4. Is home sample collection available for this test?

Yes, our VIP Mobile Phlebotomy service provides hospital-grade home collection with strict cold-chain handling. This service is available daily from 8 AM to 11 PM and is covered by many UAE insurance plans upon pre-verification.

UAE Regulatory & Data Privacy Adherence

Your health data is protected under strict regulatory frameworks. All laboratory processes comply 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. Clinical safety, patient consent, and medical liability are governed by Federal Decree-Law No. 4 of 2016 on Medical Liability. DNA Labs UAE operates under DHA Facility License Number 1143.

Clinical & Logistical Metadata

Test Name Influenza Group A & B (RNA Detection) Qualitative Test
Price (AED) 600
Turnaround Time 24-36 Hours (Phone/E-mail)
Sample Type / Matrix Nasopharyngeal Swab
Methodology Used Real-Time PCR (qPCR)
ICD-10-CM Code J10.1, J11.1
LOINC Code 76077-8
DHA Facility License & Lab Address 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE

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