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PubPharm (2.280)
91
Safety of daratumumab in the real-world : a pharmacovigilance study based on FAERS database
enthalten in:
Expert opinion on drug safety
| 2023
von
Wu, J.
|
Wu, H.
|
Chen, L.
| +6
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92
Long QT syndrome after using EGFR-TKIs in older patients with advanced non-small cell lung cancer
enthalten in:
Expert opinion on drug safety
| 2023
von
Byun, J.
|
Han, S.
|
Qdaisat, A.
| +1
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93
Model driven method for exploring individual and confounding effects in spontaneous adverse event reporting databases
enthalten in:
Expert opinion on drug safety
| 2023
von
Lv, B.
|
Li, Y.
|
Shi, A.
| +1
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94
Impact of preoperative pharmaceutical care consultation on medication errors in surgical patients : a comprehensive analysis
enthalten in:
Expert opinion on drug safety
| 2023
von
Gomez Costas, D.
|
Sánchez, A.
|
Manzorro, A.
| +6
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95
Potential side effects of currently available pharmacotherapies in male lower urinary tract symptoms suggestive of benign prostatic hyperplasia
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Expert opinion on drug safety
| 2023
von
Müderrisoglu, A.
|
de la Rosette, J.
|
Michel, M.
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96
A real-world analysis of safety profile of selexipag by using FDA adverse Event Reporting System (FAERS)
enthalten in:
Expert opinion on drug safety
| 2023
von
Zhao, J.
|
Wang, M.
|
Yu, Q.
| +3
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97
Urinary tract infections and genital mycotic infections associated with SGLT‑2 inhibitors : an analysis of the FDA Adverse Event Reporting System
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Expert opinion on drug safety
| 2023
von
Yang, T.
|
Zhou, Y.
|
Cui, Y.
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98
New exploration of signal detection of Regional Risks from the perspective of data mining : a pharmacovigilance analysis based on spontaneous reporting data in Zhenjiang, China
enthalten in:
Expert opinion on drug safety
| 2023
von
Liu, Y.
|
Xu, X.
|
Yang, J.
| +5
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99
Risk of pancreatitis and pancreatic carcinoma for anti-diabetic medications : findings from real-world safety data analysis and systematic review and meta-analysis of randomized controlled trials
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Expert opinion on drug safety
| 2023
von
Muhammed, A.
|
Thomas, C.
|
Kalaiselvan, V.
| +1
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100
Newly identified adverse events for gemcitabine using the Food and Drug Administration Adverse Event Reporting System
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Expert opinion on drug safety
| 2023
von
Zhang, W.
|
Wang, Y.
|
Jiang, X.
| +8
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Thema: Journal Article
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