BioFIRE Respiratory Panel
The BioFIRE Respiratory Panel (BRP) uses PCR technology to accurately detect 19 of the most common pathogens associated with respiratory infections including RSV, Flu, and COVID. The results do not include strep.
With one nasopharyngeal swab, the BRP can help your doctor determine what is causing your child’s illness (or your illness) and determine if further testing or interventions like antibiotics are necessary.
We will email you a copy of your results the same day. We can also fax a copy of the results to your doctor. We collect the swabs curbside, you do not have to exit your vehicle.
Culver Pediatrics Center does not offer medical advice for non-members of the practice. Once you get the BRP results, you must contact your primary care physician for medical advice or treatment. Some results may require a prescription for treatment.
3 Steps to Get Your BRP:
1) Use this link to schedule: https://calendly.com/culvernurse/biofiore
2) Use this link to complete the consent form (one per person to be tested): https://forms.gle/WqPQ53RPzAGcgavS7
3) Pay for the test by clicking the “Add to Cart” Button.
Email nurse@culverpediatrics.com for more questions.
The BioFIRE Respiratory Panel (BRP) uses PCR technology to accurately detect 19 of the most common pathogens associated with respiratory infections including RSV, Flu, and COVID. The results do not include strep.
With one nasopharyngeal swab, the BRP can help your doctor determine what is causing your child’s illness (or your illness) and determine if further testing or interventions like antibiotics are necessary.
We will email you a copy of your results the same day. We can also fax a copy of the results to your doctor. We collect the swabs curbside, you do not have to exit your vehicle.
Culver Pediatrics Center does not offer medical advice for non-members of the practice. Once you get the BRP results, you must contact your primary care physician for medical advice or treatment. Some results may require a prescription for treatment.
3 Steps to Get Your BRP:
1) Use this link to schedule: https://calendly.com/culvernurse/biofiore
2) Use this link to complete the consent form (one per person to be tested): https://forms.gle/WqPQ53RPzAGcgavS7
3) Pay for the test by clicking the “Add to Cart” Button.
Email nurse@culverpediatrics.com for more questions.
The BioFIRE Respiratory Panel (BRP) uses PCR technology to accurately detect 19 of the most common pathogens associated with respiratory infections including RSV, Flu, and COVID. The results do not include strep.
With one nasopharyngeal swab, the BRP can help your doctor determine what is causing your child’s illness (or your illness) and determine if further testing or interventions like antibiotics are necessary.
We will email you a copy of your results the same day. We can also fax a copy of the results to your doctor. We collect the swabs curbside, you do not have to exit your vehicle.
Culver Pediatrics Center does not offer medical advice for non-members of the practice. Once you get the BRP results, you must contact your primary care physician for medical advice or treatment. Some results may require a prescription for treatment.
3 Steps to Get Your BRP:
1) Use this link to schedule: https://calendly.com/culvernurse/biofiore
2) Use this link to complete the consent form (one per person to be tested): https://forms.gle/WqPQ53RPzAGcgavS7
3) Pay for the test by clicking the “Add to Cart” Button.
Email nurse@culverpediatrics.com for more questions.
Viruses Detected: Adenovirus, 5 Coronaviruses including COVID19, Human Metapneumovirus, Rhinovirus/Enterovirus, 5 Influenza Types, 4 Parainfluenza Types, RSV
Bacteria Detected: Bordatella parapertussis, Bordatella pertussis (whooping cough), Chlamydia pneumoniae, Mycoplasma pneumoniae (“walking pneumonia”)
*This product has not been FDA cleared or approved, but has been authorized for emergency use by FDA under an Emergency Use Authorization (EUA) for use by authorized laboratories; This product has been authorized only for the detection and differentiation of nucleic acid of SARS-CoV-2 from multiple respiratory viral and bacterial organisms; and, The emergency use of this product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug, and Cosmetic Act, 21 U.S.C. § 360bbb-3(b)(1), unless the declaration is terminated or authorization is revoked sooner.