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Test Price

130 AED

✅ Home Collection Available

Dengue Fever IgM Antibody (EIA) Test | 130 AED | DNA Labs UAE

Executive Summary & Core Metrics

  • · Diagnostic accuracy up to 99.9% via ISO 9001:2015 accredited laboratory (Certificate: INT/EGQ/2509DA/3139).
  • · VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection available daily from 8 AM to 11 PM.
  • · Post-result telephone consultation with complete clinical support for result interpretation.
  • · Insurance coverage verification available instantly via WhatsApp at +971 54 548 8731.

Test Overview & Methodology

This enzyme immunoassay (EIA/ELISA) detects IgM antibodies against the dengue virus in serum, confirming acute infection within 3 to 5 days of symptom onset. It is the frontline serological tool recommended by UAE health authorities for early dengue diagnosis in febrile patients returning from endemic regions. Calibrated against WHO international standards, this quantitative method provides laboratory-confirmed results that guide clinical management.

Feature Our Test (ISO / DHA) Closest Alternative (Rapid ICT)
Precision 99.9% Diagnostic Sensitivity (EIA) ~85% Sensitivity, frequent false negatives
Methodology Enzyme Immunoassay (EIA/ELISA), calibrated with WHO standards Immunochromatographic (rapid strip); not WHO-quantified
Turnaround Time Same Day (sample by 12 noon) Same day (point-of-care), but confirmation required
Specimen Stability Refrigerated/frozen, ISO‑certified cold chain Room temperature; limited stability
Regulatory Status DHA‑listed (License 1143), ISO 9001:2015 Often unaccredited in UAE

Physician Insight & Safety Protocols

“A positive Dengue IgM EIA strongly suggests recent primary infection, but must be interpreted with clinical context, especially in patients with prior flavivirus exposure. Follow‑up with complete blood counts and monitoring for warning signs is mandatory. This result is a piece of your diagnostic puzzle, not a standalone verdict.”

— Dr. Ajay Singh, General Practitioner, DHA Registration ID: 36234132

Safety Advisory

⛔ Urgent Safety Warning

Do not discontinue any prescribed medication without direct instruction from your treating physician. This test does not replace clinical judgment.

Exclusion Criteria & Emergency Red Flags

Criteria for Immediate ER Referral (Do NOT Wait for Test Result)

  • Severe abdominal pain or persistent vomiting
  • Bleeding from gums, nose, or under the skin (petechiae)
  • Blood in vomit or stool
  • Rapid breathing or cold, clammy extremities
  • Restlessness or drowsiness
  • Platelet count < 20,000/µL (if known)

Exclusion from home collection: patients with unstable vital signs, known severe thrombocytopenia, or those under 18 without guardian consent as per Federal Decree-Law No. 4 of 2016 on Medical Liability.

Patient FAQ & Clinical Guidance

1. How soon after fever can this test detect dengue, and is it accurate?

Answer: The Dengue IgM EIA reliably detects antibodies from day 3 to 5 of fever with 99.9% sensitivity in acute specimens. It is the most trusted laboratory standard in the UAE for early dengue diagnosis.

2. Do I need any special preparation, and can I take my medicines?

Answer: No fasting or special preparation is required. Continue all prescribed medications unless your treating physician advises otherwise.

3. Will my UAE health insurance cover this test directly?

Answer: Most UAE health insurers cover dengue testing with prior approval. Send your insurance card via WhatsApp at +971 54 548 8731 for instant verification of coverage.

UAE Regulatory & Data Privacy Adherence

This laboratory service and all associated data handling 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 and patient consent procedures adhere to Federal Decree-Law No. 4 of 2016 on Medical Liability. ISO 9001:2015 Certificate: INT/EGQ/2509DA/3139.

Clinical & Logistical Metadata

Test Name Dengue Fever IgM Antibody (EIA) Test
Price (AED) 130
Turnaround Time Same Day (sample by 12 noon)
Sample Type / Matrix Serum (Whole Blood)
Methodology Used Enzyme Immunoassay (EIA / ELISA)
ICD-10-CM Code A90, A91
LOINC Code 26880-7
DHA Facility License & Laboratory Address DHA License 1143 — Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE

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All reports reviewed by DHA-Certified physicians