1 of 7

Pharmacogenomics Kit - Personalized Medicine DNA Test Kit

Pharmacogenomics Kit - Personalized Medicine DNA Test Kit

Personalized DNA check with insights into drug response and treatment optimization

The Pharmacogenomics Kit is a simple, non-invasive buccal swab DNA test, that helps uncover how your genes influence your response to medications. By analyzing key genetic variants, this kit empowers your doctor to personalize your treatment plan, choosing the right medicine, at the right dose, with fewer side effects. Pharmacogenomics testing can make your healthcare smarter, safer, and more effective.

Includes Test Kit Delivery and pickup / Extensive Pharmacogenomics analysis report / Free Expert Consultation

Benefits

  • Personalized Medicine – Identify which drugs are likely to work best for you.
  • Safety First – Reduce risk of adverse drug reactions and side effects.
  • Optimized Dosage – Helps doctors prescribe the right drug at the right dose.
  • Faster Relief – Avoid the trial-and-error method of prescribing.
  • Comprehensive Insights – Covers genetic response to ~150 – 200 FDA-approved drugs for various diseases.
  • Non-Invasive & Easy – Simple buccal swab, no blood needed.
Regular price ₹8,499.00
Regular price MRP ₹9,999.00 Sale price ₹8,499.00
Sale Sold out
Inclusive of all taxes. Shipping calculated at checkout.
Select A Pack - Buy More Save More
View full details
  • Icon
    100% Privacy Guaranteed
  • Icon
    We use
    plain boxes
  • Icon
    Product name is not displayed
  • Payment_options_to_buy_Moderate_tablets 100% Quality Guarantee
  • Payment_options_to_buy_Moderate_tablets COD Available
  • Payment_options_to_buy_Moderate_tablets Free Delivery
  • Payment_options_to_buy_Moderate_tablets Expert consultation with Dietician
Payment_options_to_buy_Moderate_tablets

Manufactured by: STIRITI AYUR THERAPIES PVT. LTD. H No. 3-20 Sy no. 179 & 180, Cheekatimamidi (V), Bommalarammaram (M), Yadadri (D), Telangana-508116. AYUSH Mfg. Lic. No. : T-2340/Ayurv.

Marketed By: INU ENERGY PRIVATE LIMITED, 5th Floor, Unit 2a/1 (octave Block), Salarpuria Sattva Knowledge City, Madhapur, Hyderabad, Telangana, India, 500081.

Manufactured by: Virchow Biotech Private Limited Unit-IV, Sy.No.10/LU,10/LU2, Gaddapotharam(V), Jinnaram(M), Sangareddy, Telangana-502319.
Fssai 10021047000252

Marketed By: INU ENERGY PRIVATE LIMITED, 1st Floor, Plot No. 36, House No. 5-9-287/36, Rajiv Gandhi Nagar, Moosapet, Kukatpally Circle No 24, Hyderabad, Telangana, India, 500072
Fssai 13624999000079

  • Order your Test

    Step 01

    Order you test

  • Receive the kit at your house address

    Step 02

    Receive the kit at your house address

  • Collect your Buccal / mouth swab within 2 days of receiving the kit

    Step 03

    Collect your Buccal / mouth swab within 2 days of receiving the kit

  • Connect with Moderate Team to schedule the reverse pick up of sample

    Step 04

    Connect with us so that we can schedule the reverse pick up of sample

What to Expect

About 3–4 weeks after we receive your cheek swab sample, you’ll get an email and WhatsApp notification that your personalized "Pharmacogenomics Report" is ready. Here’s what happens behind the scenes:

  • WEEK
    1

    Sample Collection & DNA Extraction

    • We receive your buccal swab sample.
    • Our lab team extracts DNA from your buccal sample with the highest quality standards.
    • Your sample is assigned a unique ID to ensure secure and confidential processing.
  • WEEK
    2

    Genotyping & Sequencing

    • Your DNA is analyzed using advanced Next-Generation Sequencing (NGS) / high-resolution genotyping platforms.
    • We scan key gene variants (such as CYP2D6, CYP2C19, SLCO1B1, TPMT, etc.) known to affect drug response.
    • Rigorous quality control ensures accuracy and reliability of results.
  • WEEK
    3

    Pharmacogenomic Analysis

    • Our bioinformatics team matches your genetic profile with ACMG/AMP GATK, CPIC approved guidelines.
    • We identify how your genes influence your response to cardiac drugs, antidepressants, painkillers, cholesterol-lowering agents, cancer therapies, and more.
    • Each result is reviewed by genetic experts for clinical accuracy.
  • WEEK
    4

    Personalized Report & Counseling

    • You receive a comprehensive, easy-to-understand Pharmacogenomics Report.
    • The report highlights:
      • Which medicines are most effective for you
      • Which medicines may cause side effects
      • Recommended dose adjustments (if applicable)
    • Our certified genetic counselor connects with you to explain results and guide you (and your doctor) on next steps for personalized treatment decisions.

✨ This ensures you move from a “one-size-fits-all” prescription to a tailored medicine plan for a safer and effective treatment goals.

Frequently Asked Questions (FAQs)

What is pharmacogenomics testing?

Pharmacogenomics (also called pharmacogenetics) is the study of how your genes affect your response to medicines. By analyzing specific genetic variants, this test helps doctors choose the right drug, in the right dose, while reducing side effects.

How is the test performed?

The test is done using a simple buccal swab (cheek swab). No needles or blood draw are required. Your DNA is extracted from cheek cells and analyzed using Next-Generation Sequencing (NGS) or high-resolution genotyping platforms.

How is this different from a regular health check-up?

Routine check-ups measure your current health status (cholesterol, sugar, liver function, etc.). Pharmacogenomics looks at your genetic blueprint, which does not change with time, and predicts how your body will respond to medicines now and in the future.

Which medicines are covered in this test?

The test evaluates genes that influence responses to drugs in multiple therapeutic areas:

  • Cardiovascular – Blood thinners (warfarin, clopidogrel), anticoagulants (apixaban, dabigatran, rivaroxaban), anti-arrhythmics (flecainide, propafenone), antihypertensives (beta-blockers, ACE inhibitors, ARBs, diuretics, calcium-channel blockers), and statins (atorvastatin, rosuvastatin, simvastatin, pravastatin, lovastatin).
  • Psychiatric – Antidepressants (sertraline, fluoxetine, venlafaxine, paroxetine, amitriptyline, escitalopram, citalopram, duloxetine, etc.) and antipsychotics (risperidone, olanzapine, clozapine, quetiapine, aripiprazole, lithium).
  • Pain management – Analgesics/NSAIDs (acetaminophen, naproxen, sulindac) and opioids (tramadol, oxycodone, methadone, fentanyl, tapentadol, buprenorphine).
  • Diabetes – Metformin, sulfonylureas (glimepiride, gliclazide, glibenclamide, glipizide), DPP-4 inhibitors (sitagliptin, vildagliptin, linagliptin), SGLT2 inhibitors (empagliflozin, dapagliflozin, canagliflozin), GLP-1 agonists (liraglutide, semaglutide), and thiazolidinediones (pioglitazone, rosiglitazone).
  • Oncology (cancer therapy) – Chemotherapy agents such as mercaptopurine (TPMT variants), irinotecan (UGT1A1 variants), and targeted therapies like trastuzumab (HER2 status), with side-effect and toxicity risk prediction.
  • Immunology & Transplant – Immunosuppressants including azathioprine, tacrolimus, cyclosporine, mycophenolate, and biologics (adalimumab, infliximab, etanercept) used in autoimmune conditions and post-transplant care.
  • Other conditions – Gastrointestinal (PPIs such as omeprazole, esomeprazole, lansoprazole, pantoprazole), antiemetics (granisetron, palonosetron), asthma (tiotropium, glucocorticoids), and anti-inflammatory/arthritis drugs (methotrexate, allopurinol, TNF-inhibitors).

How accurate is the test?

Our test follows internationally recognized guidelines (ACMG/AMP GATK, CPIC). The sequencing is performed at >95% coverage and high depth to ensure robust and clinically relevant results. However, genetic testing is one piece of information and should always be interpreted along with your medical history and doctor’s advice.

Is pharmacogenomic testing useful for everyone?

Yes. Even healthy individuals can benefit by knowing how their body may react to common medicines in the future. For patients already on multiple medications, it helps avoid trial-and-error prescribing and prevents adverse drug reactions.

How long does it take to get results?

From the time we receive your swab sample, it takes 3–4 weeks to process, analyze, and deliver your comprehensive pharmacogenomics report. You will also get a counseling session to explain the findings.

Is this test approved and recognized in India and the USA?

  • Pharmacogenomic interpretations are based on ACMG/AMP GATK, CPIC Guidelines.
  • This test can be used for clinical screening and research purposes only. The test is registered in CDSCO, India, as Uppalu-Hyder-TE/M/IVD/008407, Class C of Medical Devices, 2022.

Will this test tell me which disease I will get in the future?

No. This test does not predict diseases. Instead, it predicts how your body responds to medicines for various conditions. Some comprehensive panels may also combine disease-risk insights, but pharmacogenomics is focused on drug response and safety.

Who should consider this test?

  • People starting long-term medicines (cholesterol, diabetes, depression, hypertension etc.)
  • Patients with a history of drug side effects.
  • Individuals who take multiple medicines.
  • Cancer patients considering chemotherapy.
  • Anyone interested in personalized medicine and preventive healthcare.

Customer Reviews

Based on 12 reviews
100%
(12)
0%
(0)
0%
(0)
0%
(0)
0%
(0)
P
Pratap Reddy
Amazing Test

I was amazed when i saw the results of the test. So much information about so many medicines. My doctor was also very happy to see the report and prescribed medicine for my diabetes from the list of medicines that will work for me. Thank you.

S
Sanjana
So Affordable

I cant beleive that such a fantastic test with so many importat repors costs so less. Really great.

N
Naina
No more acidity

No antacid seemed to work, and I kept switching brands. Thanks to the DNA test, we found out I metabolize those drugs unusually fast. My doctor gave me a different medicine and my acidity is finally gone.

S
Surendra
Geat Help

The process was easy and the report was clear. It helped my family avoid medicines with a high risk of allergy and side effects. A game-changer for us

D
Dinesh
Was scared

I was scared to use blood thinners because of my family’s history of side effects. This test helped my doctor pick the safest option for me, so I’m protected without any unnecessary risks.”