Test Price
2,200 AED✅ Home Collection Available
Imipramine Serum Test in UAE | 2200 AED | Therapeutic Drug Monitoring
Executive Summary & Core Metrics
Clinical Executive Summary
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Accuracy Guarantee: 99.9% Diagnostic Sensitivity via LC-MS/MS methodology, processed in an ISO 9001:2015 accredited facility (Cert: INT/EGQ/2509DA/3139).
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Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection (Available daily from 8 AM to 11 PM).
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Clinical Guidance: Telephonic Post-Test Clinical Guidance is provided to support result interpretation with your referring physician.
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Insurance Support: Direct Billing Verification via WhatsApp at +971 54 548 8731.
Test Overview & Methodology
The Imipramine Serum Test precisely quantifies the level of imipramine, a tricyclic antidepressant (TCA), in your blood. This therapeutic drug monitoring (TDM) assay is critical for ensuring the drug concentration stays within the narrow therapeutic window—maximizing efficacy for major depressive disorder or nocturnal enuresis while vigilantly preventing potentially fatal cardiotoxicity, nephrotoxicity, or neurotoxicity associated with supratherapeutic levels.
| Feature | Our Test (DNA Labs UAE) | Closest Alternative (Regional Lab) |
|---|---|---|
| Precision Technology | LC-MS/MS | Immunoassay or HPLC-UV |
| Analytical Speed | Batch Processing; Results in 2-3 Weeks | Often 4-6 Weeks (Outsourced) |
| Clinical Specificity | Superior specificity; no cross-reactivity with metabolites | Potential cross-reactivity, overestimating levels |
Physician Insight & Safety Protocols
“As a general practitioner, I see therapeutic drug monitoring as a critical safety tool. An imipramine level is not just a number; it guides dose adjustments to prevent toxicity. I always review the patient’s clinical status, ECG, and side effect profile before making any changes. The goal is to achieve effective treatment without risking cardiac or neurological complications.”
— Dr. Ajay Singh | General Practitioner | DHA Registration ID: 36234132
Critical Medication Warning
Do not discontinue, modify, or supplement your prescribed imipramine dosage based on this or any lab result without explicit consultation with your prescribing doctor. Abrupt cessation of TCAs can precipitate a severe withdrawal syndrome, including cardiac arrhythmias and rebound depression.
Safety Exclusion Criteria & Emergency Red Flags
- Exclusion: Patients who have ingested the test dose less than 12 hours prior—wait to ensure accurate post-dose steady-state sampling.
- Exclusion: Use of SST (Serum Separator Tube) gel barriers; strictly Red Top (No Additive) tube only is mandated.
- Red Flag: If you experience new-onset, unexplained syncope, seizure, or severe palpitations before your collection, proceed directly to the nearest Emergency Department for an immediate ECG.
Patient FAQ & Clinical Guidance
1. Why is my psychiatrist ordering this test instead of just relying on my symptoms?
A therapeutic blood level monitoring ensures your dose achieves remission without toxicity, because Tricyclic Antidepressants like Imipramine have a dangerously narrow window.
2. What does the “>12 hours post oral dose” pre-test requirement mean for me?
This instruction means you must take your last dose exactly 12 to 14 hours before our phlebotomist draws your blood sample in the morning.
3. Why does my report take 2-3 weeks, and is it a valid wait?
The 2-3 week turnaround time is due to high-complexity batch analysis via LC-MS/MS, which is a highly sensitive, reference-level method ensuring 99.9% accuracy for your safety.
UAE Regulatory & Data Privacy Adherence
This service complies with:
- Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) for complete data privacy.
- 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 for clinical testing safety and patient consent.
Clinical & Logistical Metadata
| Test Name | Imipramine Serum Test |
| Price (AED) | 2,200 AED |
| Turnaround Time | 2-3 Weeks |
| Sample Type / Matrix | Serum |
| Methodology Used | LC-MS/MS |
| ICD-10-CM Code | Z51.81 |
| LOINC Code | 3538-7 |
| DHA Facility License & Laboratory Address Invariants | License: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE | DNA Labs UAE |
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All reports reviewed by DHA-Certified physicians