792 results match your criteria: "Centre Regional de Pharmacovigilance[Affiliation]"
Therapie
January 2025
Centre régional de pharmacovigilance, hôpital Nord, CHU de Saint-Étienne, 42055 Saint-Étienne cedex, France.
Aim: During coronavirus disease 2019 (COVID-19), the incidence rate of adverse drug reactions (ADRs) in hospitalized patients seemed higher than before the pandemic. Severe inflammation triggered by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was cited as an explanation. We aimed to determine whether COVID-19 infection was associated with a higher risk of ADRs compared to other infectious diseases.
View Article and Find Full Text PDFCephalalgia
January 2025
Service de Pharmacologie Clinique, Centre Régional de Pharmacovigilance, CHU Poitiers, Poitiers, France.
J Antimicrob Chemother
January 2025
Department of Infectious Diseases, CHU de Saint-Etienne, Saint-Etienne 42055, France.
Background: Antibiomania is the manifestation of manic symptoms secondary to taking an antibiotic, which is a rare side effect. In these cases, the antibiotics most often incriminated are macrolides and quinolones, but to our knowledge, there are no published cases of antibiomania secondary to cotrimoxazole. Furthermore, we also provide an update of pharmacovigilance data concerning antibiomania through a search of the World Health Organization (WHO) database.
View Article and Find Full Text PDFTherapie
December 2024
Équipe AHeaD, CHU de Bordeaux, service de pharmacologie clinique, BPH, université de Bordeaux, Inserm U1219, 33000 Bordeaux, France.
The drug authorization process is shifting towards a policy aimed at shortening time-to-market. While this policy facilitates early access to new treatments, it can also result in potentially insufficient knowledge of both efficacy and safety at the time of marketing. The latter is particularly true for long-term outcomes or in specific populations (e.
View Article and Find Full Text PDFTher Drug Monit
December 2024
Université Jean Monnet, Médecine Intensive Réanimation G, CHU Saint-Etienne, INSERM, Mines Saint Etienne, Saint-Étienne, France.
Low-dose methotrexate has been proposed as therapy for patients with severely disabling psoriasis and psoriatic arthritis. However, it can be associated with severe toxicity, such as pancytopenia, characterized by anemia (hemoglobin level <13 g/dL in men), thrombocytopenia (platelet count <150 × 109/L), and neutropenia or agranulocytosis (neutrophil count <1.5 × 109/L and 0.
View Article and Find Full Text PDFTherapie
November 2024
Service de psychiatrie 'A', CHU Hedi Chaker, 3029 Sfax, Tunisie.
Drug Saf
December 2024
Centre Régional de Pharmacovigilance, Service de Pharmacologie périnatale, pédiatrique et adulte, Hopital Cochin, Assistance Publique-Hopitaux de Paris (AP-HP), 27, rue du Faubourg Saint Jacques, 75014, Paris, France.
Introduction And Objective: Proton pump inhibitor (PPI) use in children increases the risk of infections, prompting inquiry into the impact of prenatal PPIs exposure on serious infections in offspring. As a research gap in this area exists, this study aimed to address it by assessing the association between prenatal PPIs exposure and serious infections in infants during their first year of life.
Methods: Using the French health insurance data warehouse (SNDS) (2013-2018), we conducted a retrospective cohort study on singleton, full-term liveborn non-immunocompromised infants, stratified by PPI use during the first three months of life (early-life use).
J Am Acad Dermatol
November 2024
Université de Reims Champagne-Ardenne, VIEFRA, CHU de Reims, Centre Régional de Pharmacovigilance de Reims, Reims, France.
Bull Cancer
December 2024
Département des soins de support, institut du cancer de Montpellier (ICM), Montpellier, France.
Therapie
October 2023
Service de dermatologie, hôpital Claude-Huriez, CHU de Lille, 59000 Lille, France; Service de dermatologie, groupe hospitalier Seclin-Carvin, 59113 Seclin, France.
Bull Cancer
December 2024
Pôle pharmacie, Inserm, EFS-BFC, UMR 1098, CHU de Besançon, université de Franche-Comté, 25030 Besançon, France. Electronic address:
Br J Clin Pharmacol
February 2025
CHU Besançon, INSERM, EFS-BFC, UMR 1098, Pôle Pharmacie, Université de Franche-Comté, Besançon, France.
Aims: Hospitalizations for adverse drug reactions (ADR-HA) have increased over the last decade, but the impact of ADR-HA has rarely been evaluated. The aim of this study was to estimate the economic burden of ADR-HA in France.
Methods: A partial economic evaluation from the viewpoint of French public health insurance was performed, based on a previous pharmacovigilance study (IATROSTAT) performed in 2018 in public hospital medical units.
JAMA Dermatol
December 2024
Service de Dermatologie, Hôpital Henri Mondor, Assistance Publique-Hôpitaux de Paris (AP-HP), Créteil, France.
J Investig Allergol Clin Immunol
December 2024
Service de Dermatologie, Centre Hospitalier du Mans, Le Mans, France.
Leukemia
December 2024
Caen-Normandy University Hospital, Centre Régional de PharmacoVigilance, Department of Pharmacology, Biology-Research Building, Avenue de la Côte de Nacre, F-14000, Caen, France.
Br J Haematol
September 2024
Nephrology, Dialysis and Transplantation Department, EFS, INSERM, UMR RIGHT, CHU Besançon, Université de Franche-Comté, Besançon, France.
BMC Pulm Med
September 2024
Thoracic Oncology Department, Université Paris Cité, CIC INSERM 1425, Institut du Cancer AP-HP.Nord, Hôpital Bichat-Claude Bernard, 46 Rue Henri Huchard, Paris, 75108, France.
Background: PARP inhibitors (PARPi) are used in the treatment of ovarian, breast, pancreatic, and prostate cancers. Pneumonitis has been identified as a potential side effect, with a higher meta-analysis-assessed risk for olaparib versus other PARPi. Olaparib-induced interstitial lung disease (O-ILD) was first described within the Japanese population, with few information available for Caucasian patients.
View Article and Find Full Text PDFBull Cancer
October 2024
Médecine interne et maladies-multi-organiques, centre de compétences des maladies auto-immunes, CHU de Montpellier, Montpellier, France. Electronic address:
Orthop Traumatol Surg Res
December 2024
Univ Jean Monnet, INSERM, Mines Saint-Étienne, U1059 SAINBIOSE, 42270 Saint-Étienne, France; Mines Saint-Etienne, INSERM, U1059 SAINBIOSE, Univ Jean Monnet, 42270 Saint Etienne, France.
Background: Y-TZP zirconia heads were recalled by the Food and Drug Administration (FDA) in 2001 and zirconia alone was no longer used in orthopedics. Tunnel furnace sintering was suspected of producing defects responsible for early material failure. As Zirconia Toughened Alumina (ZTA) matrices are widely used as bearing material and contain zirconia grains, there remains a need to better understand the in vivo ageing process of zirconia and its clinical implications when the material is produced by batch furnace sintering, the validated sintering process.
View Article and Find Full Text PDFJ Sleep Res
September 2024
Service Pharmacie, AP-HP, GHU Paris Nord, DMU PRISME, Hôpital Bichat-Claude Bernard, Paris, France.
J Oncol Pharm Pract
September 2024
Service de pharmacie, Pôle produits de santé, Centre Oscar Lambret, Lille, France.
Therapie
July 2024
Centre régional de pharmacovigilance, centre hospitalier universitaire de Rennes, 35000 Rennes, France.
Introduction: Cystic fibrosis transmembrane regulator (CFTR) channel modulators (ivacaftor, lumacaftor, tezacaftor and elexacaftor) represent a major advance in the management of cystic fibrosis. However, few data are available on the real-life safety profile of these medications, in particular on adverse events that may lead to their discontinuation. The aim of this study is to describe the characteristics and evolution of adverse reactions to the tezacaftor/ivacaftor/elexacaftor combination that led to discontinuation and were reported to the Centre régional de pharmacovigilance (CRPV) in Rennes (France).
View Article and Find Full Text PDFClin Chem Lab Med
November 2024
French Clinical Oncopharmacology Group (GPCO)-UNICANCER, Paris, France.