Response to FDA Adverse Event Reporting System (FAERS) Essentials: A Reflection on Study Conception. [PDF]
Reyes M, Potter E, Dal Pan G.
europepmc +1 more source
FDA Adverse Event Reporting System (FAERS) Essentials: A Guide to Understanding, Applying, and Interpreting Adverse Event Data Reported to FAERS. [PDF]
Potter E, Reyes M, Naples J, Dal Pan G.
europepmc +1 more source
Monthly buprenorphine depot injection (SUBLOCADE®) for opioid use disorder during pregnancy. [PDF]
Ramage M +3 more
europepmc +1 more source
Postmarketing adverse events of efgartigimod alfa: a real-world pharmacovigilance study based on the FAERS database. [PDF]
Ju Y, Qin X.
europepmc +1 more source
Massive Submacular Hemorrhage Following Intravitreal Faricimab Injection for Neovascular Age-Related Macular Degeneration. [PDF]
Kaganovski A, Rostomian N, Shrier E.
europepmc +1 more source
Safety of Risdiplam in Japanese Patients with Spinal Muscular Atrophy: A 12‑Month Interim Analysis of a Postmarketing Surveillance Study. [PDF]
Saito K +10 more
europepmc +1 more source
Application of fungal communitiesfinger printings to determine the geographic origin of tropical timbers [PDF]
Barbier, Georges +4 more
core
Clinical Characteristics and Safety Profiles of Japanese Psoriasis Patients Who Continued Apremilast Treatment for 6 and 12 Months: A Post Hoc Analysis of an Apremilast Postmarketing Surveillance Study. [PDF]
Ohtsuki M +8 more
europepmc +1 more source
DeepADR: multimodal prediction of adverse drug reaction frequency by integrating early-stage drug discovery information via Kolmogorov-Arnold networks. [PDF]
Wan J +7 more
europepmc +1 more source
FDA Approval Summary: Lisocabtagene Maraleucel for Relapsed or Refractory Follicular Lymphoma. [PDF]
Britton K +6 more
europepmc +1 more source

