The Rapid ResponseTM Single Drug Saliva Test Cassette is a rapid, qualitative screening test for the detection of specific drugs and drug metabolites in human oral fluid.

Product Information
  • Product Code:
  • Sample: Saliva
  • Format: Cassette
  • Specificity: Please contact us for details
  • Storage Condition: 36-86°F/2-30°C
  • Test Principle: Lateral Flow Immunoassay
Contents
  • 25 Test Cassettes
  • Product Insert
DrugACRONYMProduct CodeCUT-OFF(ng/mL)FDAFDA + CLIA WaivedHealth CanadaCE MarkInt'l
6-Monoacetylmorphine6-MAMMAM-2C11-4025
Amphetamines AMPAMP-2C13-4050
AMP-2C142-4040
Barbiturates BARBAR-2C13-4050
Benzodiazepines BZOBZO-2C13-4050
BZO-2C141-4030
BZO-2C5-4010
Buprenorphine BUPBUP-2C144-405
BUP-2C5-4010
Cocaine COCCOC-2C141-4030
COC-2C13-4050
COC-2C48-4020
Cotinine COTCOT-2C13-4050
COT-2C141-4030
Ecstasy MDMAMDM-2C13-4050
EDDP EDDPEDDP-2C48-4020
Ketamine KETKET-2C27-40100
KET-2C213-4050
Marijuana THCTHC-2C13-4050
THC-2C146-4012
Methadone MTDMTD-2C13-4050
MTD-2C141-4030
Methamphetamine METMET-2C142-4040
MET-2C13-4050
Opiate OPIOPI-2C11-4025
OPI-2C13-4050
OPI-2C142-4040
OxycodoneOXYOXY-2C13-4050
OXY-2C142-4040
OXY-2C48-4020
Phencyclidine PCPPCP-2C5-4010
PCP-2C11-4025
PCP-2C13-4050
Propoxyphene PPXPPX-2C13-4050
Synthetic Marujuana (K2)K2K2-2C13-4050
K2-2C141-4030

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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