Dengue Fever Combined Panel in UAE | 850 AED | DHA Licensed

Executive Summary & Core Metrics

The Dengue Fever Combined Panel is available at 850 AED with 99.9% diagnostic sensitivity via ISO accredited processing. Premium logistics include VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (available daily from 8 AM to 11 PM). Telephonic post-test clinical guidance is provided. Direct billing verification available via WhatsApp +971 54 548 8731.

Test Overview & Methodology

The Dengue Fever Combined Panel is a rapid immunochromatographic assay that simultaneously detects dengue NS1 antigen and IgM/IgG antibodies, enabling early diagnosis of dengue fever within 15–20 minutes. This panel aids in differentiating primary and secondary dengue infections.

Feature	Our Test (ICT Panel)	Closest Alternative (ELISA/RT-PCR)
Precision / Sensitivity	99.9% diagnostic sensitivity under ISO protocols	High analytical sensitivity but requires batched runs
Methodology	Immunochromatographic (ICT) with NS1 + IgM/IgG	ELISA or RT-PCR (laboratory-bound)
Turnaround Time	Daily (same-day results)	Typically 4–24 hours

Physician Insight & Safety Protocols

Clinical Note from Dr. Ajay Singh (DHA License: 36234132): As a General Practitioner, I recommend this panel for rapid dengue screening. However, clinical correlation with symptoms and platelet count is essential. Please consult your doctor for comprehensive management.

Safety Advisory

Do not discontinue prescribed medication without consulting your doctor.
Seek immediate emergency care if you experience: persistent vomiting, severe abdominal pain, bleeding gums, blood in vomit or stool, difficulty breathing, or sudden drop in blood pressure.

Exclusion Criteria

Do not use this test if you have a known bleeding disorder or severe thrombocytopenia without physician supervision.

Patient FAQ & Clinical Guidance

1. What is the Dengue Fever Combined Panel?

This panel is a rapid immunochromatographic test that simultaneously detects dengue NS1 antigen and IgM/IgG antibodies from serum.

2. When should I take this test?

Take it within the first 5–7 days of fever onset for optimal NS1 antigen detection, or later for antibody detection.

3. How accurate is the Dengue Fever Combined Panel?

The panel demonstrates 99.9% diagnostic sensitivity when performed by ISO-accredited labs with trained phlebotomists.

UAE Regulatory & Data Privacy Adherence

This service adheres to UAE 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 follow Federal Decree-Law No. 4 of 2016 on Medical Liability. All data is handled with ISO 9001:2015 certified privacy controls (Cert: INT/EGQ/2509DA/3139).

Clinical & Logistical Metadata

Test Name	Dengue Fever Combined Panel
Price (AED)	850
Turnaround Time	24 hours
Sample Type / Matrix	Serum
Methodology Used	Immunochromatographic (ICT) – NS1 Antigen + IgM/IgG Antibody Detection
ICD-10-CM Code	A90 (Dengue fever [classical dengue])
LOINC Code	94077-9 (Dengue virus IgG and IgM and NS1 panel – Serum)
DHA Facility License & Laboratory Address	License No: 1143 \| Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE