Showing posts with label IFTTT. Show all posts
Showing posts with label IFTTT. Show all posts

Wednesday, May 6, 2020

Coronavirus (COVID-19) Update: Daily Roundup May 6, 2020 - FDA Press Releases

Coronavirus (COVID-19) Update: Daily Roundup

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FDA Approves First Targeted Therapy to Treat Aggressive Form of Lung Cancer - FDA Press Releases

FDA approves Tabrecta (capmatinib) for the treatment of adult patients with non-small cell lung cancer (NSCLC) that has spread. Tabrecta is the first FDA-approved therapy to treat NSCLC with specific MET exon 14 skipping mutations.

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Tuesday, May 5, 2020

Monday, May 4, 2020

Friday, May 1, 2020

Coronavirus (COVID-19) Update: Daily Roundup May 1, 2020 - FDA Press Releases

Coronavirus (COVID-19) Update: Daily Roundup

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Coronavirus (COVID-19) Update: FDA Issues Emergency Use Authorization for Potential COVID-19 Treatment - FDA Press Releases

FDA has issued emergency use authorization for the investigational antiviral drug remdesivir for the treatment of suspected or laboratory-confirmed COVID-19 in adults and children hospitalized with severe disease.

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Thursday, April 30, 2020

Wednesday, April 29, 2020

Coronavirus (COVID-19) Update: Daily Roundup April 29, 2020 - FDA Press Releases

Coronavirus (COVID-19) Update: Daily Roundup

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FDA Grants Marketing of New Device for Continuous Dialysis Therapy for use in Pediatric Patients with Certain Kidney Conditions - FDA Press Releases

FDA grants marketing authorization for a new device indicated to provide continuous hemodialysis or hemofiltration therapy to critically ill pediatric patients weighing between 2.5 and 10 kilograms (or 5.5 to 22 pounds)

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Tuesday, April 28, 2020

Monday, April 27, 2020

Coronavirus (COVID-19) Update: Daily Roundup April 27, 2020 - FDA Press Releases

Coronavirus (COVID-19) Update: Daily Roundup

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FDA Warns Manufacturers and Retailers to Remove Certain E-cigarette Products Targeted to Youth from the Market - FDA Press Releases

FDA issued ten warning letters to retailers and manufacturers who sell, manufacture and/or import unauthorized electronic nicotine delivery system (ENDS) products targeted to youth or likely to promote use by youth.

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Coronavirus (COVID-19) Update: FDA Continues to Ensure Availability of Alcohol-Based Hand Sanitizer During the COVID-19 Pandemic, Addresses Safety Concerns - FDA Press Releases

FDA provides an update on its efforts to ensure the availability of alcohol-based sanitizer

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Friday, April 24, 2020

Coronavirus (COVID-19) Update: Daily Roundup April 24, 2020 - FDA Press Releases

Coronavirus (COVID-19) Update: Daily Roundup

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FDA Provides Updates on Adverse Event Reports and Postmarket Activities Associated with Essure - FDA Press Releases

FDA issued a letter to Bayer outlining conditions for submitting additional postmarket information to the agency about Essure. The letter applies to reportable adverse events Bayer is or becomes aware of from social media data received in relation to litigation.

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Coronavirus (COVID-19) Update: FDA Reiterates Importance of Close Patient Supervision for ‘Off-Label’ Use of Antimalarial Drugs to Mitigate Known Risks, Including Heart Rhythm Problems - FDA Press Releases

FDA is reiterating the importance of close patient supervision for ‘off-label’ use of antimalarial drugs to mitigate known risks, including heart rhythm problems.

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Thursday, April 23, 2020