The Rapid ResponseTM Single Drug Test Strip is a rapid, qualitative test for the detection of a selected drug in human urine. It is intended for in vitro diagnostic use only. Interpretation of test results are: positive (one line), negative (two lines), invalid (no lines or no Control line). For the alcohol strip results can be interpreted by comparison to reaction pad colors.

Product Information
  • Product Code:
  • Sample: Urine
  • Format: Strip
  • Specificity: Please contact us for details
  • Accuracy: Please contact us for details
  • Time-to-Result: 5 minutes
  • Storage Condition: 36-86°F/2-30°C
  • Test Principle: Lateral Flow Immunoassay
Contents
  • 100 Test Strips
  • Alcohol Color Chart (when applicable)
  • Product Insert
DrugACRONYMProduct CodeCUT-OFF(ng/mL)FDAFDA + CLIA WaivedHealth CanadaCE MarkInt'l
6-Monoacetylmorphine6-MAM6MAM-1S5-10010
Acetaminophen ACEACE-1S143-1005000
AlcoholALCALC-1S1-1000.02% BAC
Amphetamines AMPAMP-1S2-1001000
AMP-1S9-100500
AMP-1S3-100300
Barbiturates BARBAR-1S3-100300
BAR-1S7-100200
Benzodiazepines BZOBZO-1S9-100500
BZO-1S3-100300
BZO-1S7-100200
BZO-1S27-100100
Buprenorphine BUPBUP-1S5-10010
BUP-1S144-1005
Cocaine COCCOC-1S3-100300
COC-1S7-100200
COC-1S134-100150
COC-1S27-100100
Cotinine COTCOT-1S145-100600
COT-1S3-100300
COT-1S7-100200
COT-1S27-100100
Ecstasy MDMAMDM-1S2-1001000
MDM-1S9-100500
EDDP EDDPEDDP-1S3-100300
EDDP-1S27-100100
Ethyl GlucuronideETGETG-1S9-100500
Fentanyl FYLFYL-1S7-100200
FYL-1S48-10020
FYL-1S5-10010
HydromorphoneHMOHMO-1S147-100250
Ketamine KETKET-1S2-1001000
KET-1S9-100500
KET-1S3-100300
KET-1S27-100100
Lysergic Acid Diethylamide LSDLSD-1S13-10050
Marijuana THCTHC-1S7-100200
THC-1S134-100150
THC-1S13-10050
THC-1S11-10025
THC-1S48-10020
Methadone MTDMTD-1S3-100300
MTD-1S7-100200
Methamphetamine METMET-1S2-1001000
MET-1S9-100500
MET-1S3-100300
Methaqualone MQLMQL-1S3-100300
MethylenedioxypyrovaleroneMDPVMDPV-1S2-1001000
MethylphenidateMPDMPD-1S3-100300
Methylphenidate MetaboliteMDPMMPDM-1S2-1001000
MorphineMOPMOP-1S3-100300
MOP-1S7-100200
MOP-1S27-100100
Opiate OPIOPI-1S26-1002000
OPI-1S2-1001000
OxycodoneOXYOXY-1S3-100300
OXY-1S27-100100
Phencyclidine PCPPCP-1S11-10025
Propoxyphene PPXPPX-1S3-100300
Synthetic Marujuana (K2)K2K2-1S13-10050
Tramadol TRATRA-1S3-100300
TRA-1S27-100100
Tricyclic Antidepressants TCATCA-1S2-1001000
ZolpidemZOLZOL-1S13-10050

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Frequently Asked Questions (FAQ)

Answer: Yes, Lochness Medical Inc. Rapid Response Fecal Immunochemical Test (FIT) Kit is (FDA) Cleared and waived by the Clinical Laboratory Improvement Amendments (CLIA).

Answer: Yes, The 2008 American College Of Gastroenterology Guidelines for Colorectal Cancer Screening states: “The preferred cancer detection test is annual FIT. This test has superior performance characteristics when compared with older guaiac-based Hemoccult II cards (15 – 17) 1

Answer: Yes, the Rapid Response Fecal Immunochemical Test (FIT) Kit has an accuracy of 98%. The Guaiac based test(s) / Hemoccult Cards has an accuracy of 86%. The Guaiac based test(s) /Hemoccult Cards requires 3 stool samples on 3 different days (300,000 ng/mL sensitivity). The Rapid Response Fecal Immunochemical Test (FIT) Kit requires only 1 stool sample (50 ng/mL sensitivity). Patients must avoid Aspirin, Red meat, Vitamin C, Fruit Juices before they take a test that’s Guaiac based/Hemoccult Cards. There aren’t any dietary restrictions for the Rapid Response Fecal Immunochemical Test (FIT) Kit. Patients who conduct the FIT Test at their residence returns only the FIT Buffer Tube. The Guaiac based test(s) / Hemoccult Cards causes patients to return a stool sample, which can be messy.

Answer: The Sample Collection for the ICT may be described as messy, protracted and associated with low compliance. The Sample Collection for the FIT Test may be described as simple, one-step, hygenic and high compliance. The FIT Test is more sensitive than ICT (50 ng/mL versus 75 ng/mL).The Positive and Negative agreement between the two test approaches 100%.

Answer: No, Lochness Medical Inc. Fecal Immunochemical Test (FIT) Kit does not have any dietary restrictions.

Answer: No, Lochness Medical Inc. Fecal Immunochemical Test (FIT) Kit does not have any medical restrictions.

Answer: Store test device at room temperature (15-28°C or 59-82.4°F). Refer to the expiration date printed on the foil pouch for stability. Sample collection tube after collecting sample should be stored refrigerated (2-8°C or 35.6-46.4°F) if not used immediately.

Answer: The kit contains 36 test devices, 36 sample collection tubes, and 1 package insert.

Answer: The Rapid Response Fecal Immunochemical Test (FIT) Test Kit is 98% accurate.

Answer: No, the Rapid Response Fecal Immunochemical Test (FIT) Test is specific to human hemoglobin.

Answer: The analytical sensitivity of the Rapid Response Fecal Immunochemical Test (FIT) Test is 50 ng hHb/ml buffer or 5 ug hHb/g feces.

Answer: The false positives for the Rapid Response Fecal Immunochemical Test (FIT) Test Kit are roughly 6%. However, it is looking for human hemoglobin (blood), not paroxadais activity. When a FIT Test has a positive test result, there’s the assurance that blood is in the stool. This could be indicative of diverticulitits, colitis, Chron’s disease, hemorrids, etc.

Answer: No, the Rapid Response Fecal Immunochemical Test (FIT) Test is specific to human hemoglobin.

Answer: Yes, you can take the FIT test regardless of menstruation.

Answer: The shelf life is 24 months from the date of manufacture.

Answer: The national average insurance reimbursement for the Rapid Response Fecal Immunochemical Test (FIT) Test Kit is $21.86.

Answer: No, the CPT Codes are 82274QW for insurance and G0328QW for Medicare.

Answer: Yes, Lochness Medical Inc. offers FIT Mailers separately. The kit contains 50 FIT Mailers. The product code is FOB-9V30.

Answer: Unscrew the cap with the spiral applicator from the sample collection tube. Use the spiral applicator to poke into the stool at 6 different sites. Collect the amount necessary to only cover the grooves of the spiral applicator. More information about collecting sample specimen can be found in the FIT Mailers’ Manual/Quick Card.2

Answer: Yes, the collection paper’s material allows the convenience to flush it down the toilet.

Answer: No, the Rapid Response Fecal Immunochemical Test (FIT) Test is specific to human hemoglobin.

Answer: Specimen can be left in the collection tube for 7 days at room temperature and 14 days refrigerated.

1. Rex,MD,FACG, Douglas K., David A. Johnson, MD, FACG, Johnson C. Anderson, MD, Phillip S. Schoenfeld,MD,MSEd, MSc,(Eqi), Carol A. Burke,MD,FACG, and John M. Inadomi, MD,FACG. "American College of Gastroenterology Guidelines for." 104. (2009): n. page. Web. 11 Feb. 2014.

3. Rapid Response® (FIT) Mailers Manual/Quick card, rev. 2013