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US_FDA's Twitter statistics

Followers
556.1K
Following
145
Total Tweets
19.3K
Avg. Likes
146.9
Avg. Comments
72.8
Eng. Rate
0.59%
Est. Earning
$235.4
Fraud Score
39%

Best Time to Post

Weekly Stats

Total Tweets
0
Avg. Likes
0
Avg. Comments
0
Followers hike
556.1K

Profile Mentions

@WhiteHouse @DeptofDefense @realDonaldTrump @POTUS @USDAFoodSafety @WHO @CDCgov @Surgeon_General @NIOSH @elonmusk @NIST @POTUS @WhiteHouse @CDCMMWR

Daily Stats

Date Like Comment Post Videos Total
2023-04-22 25 16707
2023-04-21 120 70404
2023-04-20 9 48505
2023-04-19 1K 290808

Recent tweets

As of today, 445 tests and sample collection devices are authorized by the FDA under emergency use authorizations (EUAs). These include 299 molecular tests and sample collection devices, 83 antibody and other immune response tests, 62 antigen tests, and one diagnostic breath test
1 1
On Wednesday, @FDAFood released new “Feed Your Mind” educational materials to provide science-based information on genetically modified organisms (GMOs). https://t.co/UqoYNSDnDk
1 0
We also cleared the Selux AST System for use with the Selux Gram-Negative Comprehensive Panel through the 510(k) premarket notification pathway.
0 1
We also authorized for marketing the Bateman Bottle Breast Implant Removal System, a single-patient, single use suction device used to assist in the removal of one intracapsular ruptured silicone breast implant.
0 0
Yesterday, we announced we will reopen the comment period for the draft guidance entitled “Labeling of Plant-Based Milk Alternatives and Voluntary Nutrient Statements; Draft Guidance for Industry,” that appeared in the Federal Register on Feb. 23. https://t.co/a11q1W25OD
0 0
6 6
Today, we approved the MiniMed 780G System for modifications to the SmartGuard  Technology and for expanding the indications for use to include the Guardian 4 Sensor.
17 8
Read @FDAHealthEquity’s latest post for the FDA Voices Blog, authored by OMHHE Director, RDML Richardae Araojo. The blog highlights the 2023 theme for #NMHM and outlines the OMHHE Enhance Equity Initiative: https://t.co/kcbIMsHYTg #NMHM2023
4 3
13 7
All of the accounts across the agency are listed on our website here: https://t.co/eaVeRz40pF
11 6
92 54
RT @FDACBER: Our next OTP #virtual town hall is around the corner! This town hall will feature #FDA experts who can answer stakeholder ques…
0 6
RT @FDA_Drug_Info: Want to learn more about FDA regulation of cannabis and cannabis-derived products? Information for consumers, regulatory…
0 20
RT @FDAHealthEquity: Hispanics and Latinos are at a higher risk of asthma compared to other races or ethnicities. There are #ClinicalTrial…
0 9
9 6
RT @FDAanimalhealth: Hoppy #NationalFrogMonth! 🐸 Frogs and other amphibians can make good pets if you take steps to prevent Salmonella infe…
0 7
15 10
#CancerControlMonth https://t.co/owt9NYsCJB
12 4
42 23
@elonmusk Hi, Elon. Thanks for your question. It's probably worth clarifying that the monovalent vaccines are still approved (licensed). That hasn't changed. But they are no longer authorized for *emergency use* in the United States.
0.9K 242
RT @FDACosmetics: Working up a sweat on #NationalExerciseDay and refreshing yourself with wipes after your workout? Check out: https://t.co…
0 5
Yesterday, we granted marketing authorization to a system to reduce the symptoms of primary moderate-severe Restless Legs Syndrome (RLS) and improve sleep quality among drug-resistant RLS patients. It is a prescription-use only device. https://t.co/aHHdkZl7Cs
2 1
Also on Monday, @FDA_Drug_Info released a CDER Conversation about its Office of New Drugs’ Research Program, talking about the program’s important work in enhancing regulatory science research. https://t.co/IXK3ZZkxkq
4 2
As of today, 446 tests and sample collection devices are authorized by the FDA under EUAs. These include 300 molecular tests and sample collection devices, 84 antibody and other immune response tests, 61 antigen tests, and one diagnostic breath test.
8 3

Top tweets

You are not a horse. You are not a cow. Seriously, y'all. Stop it. https://t.co/TWb75xYEY4
117.3K 51.9K
Today, FDA approved the first COVID-19 vaccine for the prevention of #COVID19 disease in individuals 16 years of age and older. https://t.co/iOqsxXV1fj
91.2K 55.3K
Today FDA and @CDCgov issued a statement regarding the Johnson & Johnson #COVID19 vaccine. We are recommending a pause in the use of this vaccine out of an abundance of caution.
14.9K 14.5K
13.7K 5.7K
@JaneCoulter @dog_feelings Confirmed. I checked with @FDAanimalhealth.
11.9K 746
The vaccine also continues to be available under emergency use authorization (EUA), including for individuals 12 through 15 years of age and for the administration of a third dose in certain immunocompromised individuals.
9.4K 2.1K

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