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Test Price

130 AED

✅ Home Collection Available

Dengue Fever IgG Antibody (EIA) Test in UAE | 130 AED | DHA Licensed

Executive Summary & Core Metrics

Executive Summary

This test provides 99.9% diagnostic sensitivity for detecting past dengue virus exposure via ISO 9001:2015 accredited processing. Premium home collection is available through DHA‑licensed VIP mobile phlebotomy with temperature‑controlled cold‑chain transport, daily from 8 AM to 11 PM. Complimentary post‑test clinical guidance is provided by a DHA‑licensed physician. Direct insurance billing verification is available via WhatsApp at +971 54 548 8731.

Price: 130 AED | Turnaround Time: Same day (if sample received by noon) | Sample Type: Serum or Plasma

Test Overview & Methodology

The Dengue Fever IgG Antibody (EIA) Test uses enzyme‑linked immunosorbent assay (ELISA) to detect IgG antibodies specific to dengue virus. It is designed for seroprevalence studies and confirmation of past infection, offering high sensitivity and specificity for remote exposure assessment. This test is not intended for acute diagnosis; for current or recent infection, Dengue NS1 antigen or RT‑PCR is recommended.

Parameter Our EIA Test Rapid NS1/IgG Cassette Dengue RT‑PCR
Methodology Enzyme‑Linked Immunosorbent Assay (ELISA) Immunochromatographic lateral flow Real‑time Polymerase Chain Reaction
Diagnostic Sensitivity 99.9% ~85% >98%
Turnaround Time Same day (sample by noon) 15–20 minutes 4–8 hours
Primary Use Past/prior dengue infection, seroprevalence Acute screening (NS1 + IgG/IgM) Acute viremia, serotyping
Price (AED) 130 90–120 450–650

Physician Insight & Safety Protocols

“A positive IgG result reflects past dengue exposure and does not confirm active infection. Clinical correlation with symptoms, travel history, and acute‑phase markers like NS1 or IgM is essential. Follow‑up is recommended for patients with suspected post‑dengue fatigue syndrome.”

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

Medication Advisory

Do not discontinue prescribed medication without consulting your doctor. This test does not replace acute dengue management. Do not stop antipyretics or fluid management based on serology alone. Always follow your physician’s treatment plan.

Exclusion Criteria & Emergency Red Flags

  • Testing not indicated for patients with clear acute dengue symptoms (high fever ≤7 days) – request Dengue NS1/PCR instead.
  • Home collection deferred for individuals with severe bleeding, uncontrolled vomiting, or altered mental status.
  • Seek emergency care immediately if you experience: severe abdominal pain, persistent vomiting, bleeding gums or nose, blood in stools, extreme fatigue, or difficulty breathing.
  • This test is not validated for paediatric patients under 1 year; consult paediatrician for alternative collection.

Patient FAQ & Clinical Guidance

1. When should I take the Dengue IgG test?

The optimal window is 7–10 days after symptom onset for reliable detection of past infection. If performed earlier, repeat testing may be needed. For acute diagnosis during the first week of fever, Dengue NS1 antigen or RT‑PCR is more appropriate.

2. Does a positive IgG mean I have active dengue?

No. A positive IgG alone indicates previous exposure or past infection, not active disease. Clinical correlation and additional acute markers (IgM, NS1) are required for current illness. Your doctor will interpret the result alongside your symptoms and other lab tests.

3. Is home collection safe and DHA‑compliant?

Yes. Our VIP mobile phlebotomy is fully DHA‑licensed, cold‑chain compliant, and meets UAE health regulations. Phlebotomists follow sterile protocols and maintain ISO‑certified transport. Contact us on WhatsApp to verify your insurance coverage before booking.

4. What should I do if I have symptoms of severe dengue?

Seek emergency medical attention immediately if you experience severe abdominal pain, persistent vomiting, bleeding, or difficulty breathing. This test is not for acute management; do not rely on serology results in an emergency.

UAE Regulatory & Data Privacy Adherence

Regulatory Compliance: This test is performed in strict adherence to:

  • Federal Decree‑Law No. 45 of 2021 on Personal Data Protection (PDPL)
  • Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields
  • Federal Decree‑Law No. 4 of 2016 on Medical Liability
  • Dubai Health Authority (DHA) regulatory standards for laboratory testing and home phlebotomy services

All patient data is encrypted and processed under UAE data protection laws. Samples are handled through ISO‑certified cold‑chain logistics.

Clinical & Logistical Metadata

Test Name Dengue Fever IgG Antibody (EIA) Test
Price (AED) 130
Turnaround Time Same day by 6 PM (if sample received before noon)
Sample Type / Matrix Serum or Plasma (venous blood) – VIP Mobile Phlebotomy & Temperature‑Controlled Cold‑Chain Home Collection available daily 8 AM–11 PM
Methodology Used Enzyme‑Linked Immunosorbent Assay (ELISA)
ICD‑10‑CM Code A90 (Dengue fever), Z86.19 (Personal history of dengue)
LOINC Code 3030‑5 (Dengue virus IgG Ab [Units/volume] in Serum)
DHA Facility License & Address DHA License No: 1143
Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE
Corporate Lab: DNA Labs UAE

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