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What is the role of antineoplastic drug safety in reimbursement decision making?
Published 2018-11-01Subjects: “…drug safety…”
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Risk of Thrombocytopenia by SSRIs or SNRIs in Patients With Depression Based on MID‐NET: A Cohort Study in Japan
Published 2025-06-01Subjects: Get full text
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Zolpidem’s insidious potential of abuse: A word of caution
Published 2024-07-01Subjects: Get full text
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Levofloxacin: Analysis of Information on Adverse Reactions from Russian Spontaneous Report Database
Published 2020-05-01Subjects: Get full text
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Safety profiles of biosimilars vs. their EU reference products: INNs (adalimumab, bevacizumab, trastuzumab, rituximab, infliximab, etanercept)
Published 2025-07-01Subjects: Get full text
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Evaluating the Equity of Female Representation for Determining the Safety and Efficacy of Ibuprofen: An Analysis of the Supporting Evidence for Canadian Ibuprofen Product Monograph...
Published 2024-04-01Subjects: “…drug safety…”
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Review of the monograph by Kolbin A. S., Zyryanov S. K., Belousov D. Yu. "Pharmacovigilance" 2025
Published 2025-01-01Subjects: Get full text
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A narrative review of veterinary pharmacovigilance situations and prospects in East African countries
Published 2024-11-01Subjects: Get full text
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Nanoscale Therapeutic System: Safety Assessment Features
Published 2019-09-01Subjects: “…drug safety…”
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VARENICLINE IN PATIENTS WITH CARDIOVASCULAR DISEASES – FRIEND OR ENEMY?
Published 2015-09-01Subjects: Get full text
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Mining and analysis of dizziness adverse event signals in postoperative analgesia patients based on the FDA adverse event reporting system database
Published 2025-02-01Subjects: Get full text
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Methotrexate in Rheumatoid Arthritis: Effect on Blood, Liver and Renal Laboratory Parameters
Published 2015-12-01Subjects: “…Rheumatoid arthritis, Methotrexate, Laboratory parameters, Monitoring, Response, Drug safety…”
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High Dose Selection for General Toxicity Studies of New Medicines
Published 2023-06-01Subjects: Get full text
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Neurological adverse events associated with baclofen: a pharmacovigilance study based on FDA adverse event reporting system
Published 2025-05-01Subjects: Get full text
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