Results 51 to 60 of about 36,199 (325)

Quality of Clinical Information in Pregnancy Pharmacovigilance Data Sources-A Contribution of the ConcePTION Project. [PDF]

open access: yesPharmacoepidemiol Drug Saf
ABSTRACT Purpose Good documentation of adverse events related to medicines is essential for the assessment of safety signals. Information on the clinical quality of primary pregnancy safety data sources is lacking. The objective of this study was to assess the differences in clinical quality of various sources of primary pregnancy pharmacovigilance (PV)
van Rijt-Weetink YRJ   +7 more
europepmc   +2 more sources

Control yourself: ISPE‐endorsed guidance in the application of self‐controlled study designs in pharmacoepidemiology

open access: yesPharmacoepidemiology and Drug Safety, 2021
Consensus is needed on conceptual foundations, terminology and relationships among the various self‐controlled “trigger” study designs that control for time‐invariant confounding factors and target the association between transient exposures (potential ...
S. Cadarette   +9 more
semanticscholar   +1 more source

Interactive exploration of population scale pharmacoepidemiology datasets

open access: yes, 2020
Population-scale drug prescription data linked with adverse drug reaction (ADR) data supports the fitting of models large enough to detect drug use and ADR patterns that are not detectable using traditional methods on smaller datasets. However, detecting
Abadi M.   +4 more
core   +1 more source

Concepts of Designing and Implementing Pharmacoepidemiology Studies on the Safety of Systemic Treatments in Dermatology Practice

open access: yesJID Innovations, 2023
The U.S. Food and Drug Administration and clinical guidelines use evidence from pharmacoepidemiology studies to inform prescribing decisions and fill evidence gaps left by randomized controlled trials (RCTs).
Sebastian Schneeweiss   +1 more
doaj  

Time‐related biases in perinatal pharmacoepidemiology: A systematic review of observational studies

open access: yesPharmacoepidemiology and Drug Safety, 2022
Time‐related biases, such as immortal time and time‐window bias, frequently occur in pharmacoepidemiologic research. However, the prevalence of these biases in perinatal pharmacoepidemiology is not well understood.
U. Ukah   +5 more
semanticscholar   +1 more source

Trends and uptake of new formulations of controlled-release oxycodone in Canada [PDF]

open access: yes, 2018
Purpose: This study investigated the impact of changing availability of tamper‐deterrent and non‐tamper‐deterrent oxycodone on prescribing patterns of controlled‐release oxycodone across Canada.
Caetano, Patricia   +6 more
core   +2 more sources

Response to "Aromatase Inhibitors and Dementia Risk: Putting Safety Into Perspective". [PDF]

open access: yesPharmacol Res Perspect
Pharmacology Research &Perspectives, Volume 13, Issue 3, June 2025.
Yuste MT   +3 more
europepmc   +2 more sources

Pharmacoepidemiology in pregnancy

open access: yesTherapies, 2019
Taking a medication is usually a challenge for a pregnant woman as the beneficial drug effect on the mother has to be considered regarding its potential adverse effects, not only for her but also for her unborn child. As medication use is common in pregnant women, by chance or necessity, it gives the opportunity to evaluate the consequences of prenatal
Agnès Sommet   +6 more
openaire   +4 more sources

Immunosuppressants and risk of Parkinson disease [PDF]

open access: yes, 2018
We performed a population-based case-control study of United States Medicare beneficiaries age 60-90 in 2009 with prescription data (48,295 incident Parkinson disease cases and 52,324 controls) to examine the risk of Parkinson disease in relation to use ...
Camacho-Soto, Alejandra   +5 more
core   +2 more sources

Do case-only designs yield consistent results across design and different databases? A case study of hip fractures and benzodiazepines. [PDF]

open access: yes, 2015
BACKGROUND: The case-crossover (CXO) and self-controlled case series (SCCS) designs are increasingly used in pharmacoepidemiology. In both, relative risk estimates are obtained within persons, implicitly controlling for time-fixed confounding variables ...
Alvarez, Arturo   +16 more
core   +8 more sources

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