article thumbnail

Rite Aid Addresses Cyberattack: 2.2 Million Customers’ Data Breached

Drug Topics

The retail pharmacy chain issued an alert to its customers that purchasing data from 2017 to 2018 may have been breached by a third party.

524
524
article thumbnail

FDA: Fasenra Approved As Add-On Maintenance Therapy for Severe Pediatric Asthma

Drug Topics

Fasenra was initially approved in 2017 as an add on maintenance therapy in patients aged 12 years and older.

FDA 387
Insiders

Sign Up for our Newsletter

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.

article thumbnail

STAT+: Life sciences deals on track to hit lowest point since 2017

STAT

If dealmaking remains consistent for the rest of the year, it would put this year on par with the number of deals made in 2017. For comparison, there were roughly 2,122 financing deals made last year. Continue to STAT+ to read the full story…

132
132
article thumbnail

Preserving Patient Access to Compounded Medications Act of 2017

Pharmacy Times

The act would have permitted health care facilities to stock up on compounded medications without forcing the supplying 503A pharmacies to register as outsourcing facilities.

article thumbnail

Adderall Shortage Led to More Alternative Stimulant Prescriptions for US Children

Drug Topics

Researchers analyzed overall prescription stimulant dispensing trends among US children from 2017 to 2023.

247
247
article thumbnail

STAT+: FTC slams PBMs for boosting specialty drug prices at the expense of the U.S. health care system

STAT

billion in revenue by dispensing medicines to treat cancer, HIV, heart disease and other serious illnesses at prices that exceeded their estimated acquisition costs between 2017 and 2022. Specifically, the companies were able to generate more than $7.3 Continue to STAT+ to read the full story…

Insurance 140
article thumbnail

STAT+: Two of FDA’s top cancer regulators to depart, heightening worries about drug reviews

STAT

The FDA’s Oncology Center of Evidence was created in 2017 by Congress as a way to speed the development of cancer treatments. Theoret, who joined as a medical reviewer in 2009, have told colleagues of plans to leave the FDA, multiple sources familiar with the matter told STAT.

FDA 105