Flowflex Covid-19 Ag Home Test coupons
Covid-19 At Home Antigen Test

Flowflex Covid-19 Ag Home Test Coupons & Savings Card – Discount Prices from $157.44

Brand for: Covid-19 at home antigen test

A home antigen test for COVID-19 that provides quick results, suitable for initial screening of the virus.
Our Flowflex Covid-19 Ag Home Test coupons are free to use. You can print the coupon, email it to yourself, or receive the Flowflex Covid-19 Ag Home Test coupon via text message. To get your free discount, show the pharmacist your Flowflex Covid-19 Ag Home Test savings card which has the discounted coupon price. Use our filters below to edit the prescription box to match your needs. The Flowflex Covid-19 Ag Home Test prices will update based on your prescription needs. Above our Flowflex Covid-19 Ag Home Test coupons, you can change the location to see pharmacy prices in other areas. Our prescription discount card will update online with the specific pharmacy costs associated with your edits. Be sure to text, email, or print the Flowflex Covid-19 Ag Home Test savings card code that you need after editing the prescription box and location field. Show the discount card to your pharmacist before paying.

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1, Covid-19 At Home Antigen Test (30 Kits)

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Walgreens

$157.44

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Flowflex Covid-19 Ag Home Test savings card

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Walgreens

$157.44

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019876

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Flowflex Covid-19 Ag Home Test dosage forms

Use our Flowflex Covid-19 Ag Home Test 1 coupon with prices from $157.44 for 30 Kits.
DosageQuantityPrice fromPer unit
130 Kits$157.44$5.25

Our price history data is based on aggregated prescription data collected from participating pharmacies in America. Our prescription data updates daily to reflect the latest price changes. If you notice a missing data point, it means there wasn't sufficient data available to generate a monetary value for that date.

Flowflex Covid-19 Ag Home Test FAQs
Is flowflex COVID-19 antigen home test accurate?

The Flowflex COVID-19 Antigen Home Test is considered to be a reliable option for detecting the presence of the virus. It has been authorized for emergency use by the FDA and has demonstrated a high level of accuracy in identifying positive cases, particularly when the viral load is high. However, like all antigen tests, it may have a lower sensitivity compared to PCR tests, which means there is a possibility of false negatives. It is important to follow the instructions carefully and consider confirmatory testing if symptoms persist or if there is a high suspicion of COVID-19 despite a negative result.

Flowflex COVID-19 Antigen Home Tests were recalled due to concerns about the potential for false positive results. The recall was initiated to ensure the accuracy and reliability of the test results, as false positives could lead to unnecessary quarantine or treatment. It is important for users to check the lot numbers of their tests to determine if they are affected by the recall and to follow any guidance provided by the manufacturer or health authorities.

The Flowflex COVID-19 test is designed to detect the presence of the SARS-CoV-2 virus, including the Omicron variant. While no test is 100% accurate, the Flowflex test has been shown to be effective in identifying COVID-19 infections, including those caused by the Omicron variant. It is important to follow the test instructions carefully and consider confirmatory testing if symptoms persist or if there is a high suspicion of infection despite a negative result.

Flowflex, like any diagnostic test, has the potential to give false negative results. This means that the test may indicate a person does not have the condition when they actually do. Factors that can contribute to false negatives include testing too early in the course of an infection, improper sample collection, or low viral load at the time of testing. It is important to follow the test instructions carefully and consider retesting if symptoms persist or if there is a high suspicion of infection.

Yes, the Flowflex COVID-19 Antigen Home Test has received Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA).