Results 261 to 270 of about 38,036 (299)

Assessing Adverse Drug Reactions Reported for New Respiratory Medications in the FDA Adverse Event Reporting System Database

Respiratory Care, 2021
BACKGROUND: Between 2012 and 2017, 25 new medications or combination products were approved by the Food and Drug Administration (FDA) for use in treatment of chronic lower respiratory diseases (CLRDs). With limited data on post-marketing patient exposure to these drugs, their safety profiles remain unknown. This
Hyunwoo, Kim, Colin M, Pfeiffer, Matthew P, Gray, Britney A, Stottlemyer, Richard D, Boyce, Sandra L, Kane-Gill   +5 more
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Patient satisfaction with a hospital adverse drug reaction reporting system

Journal of Pharmacy Practice and Research, 2020
AbstractAimTo evaluate patients' satisfaction with the adverse drug reactions (ADR) warning card model used within a metropolitan hospital network in Melbourne, Australia.Methods and ResultsA cross‐sectional survey, with interviewer‐administered questionnaire, of patients who experienced an ADR was conducted.
Matthew W. Scott, Michael McDonough, Grace O. Wong, Richard Summers, Marion Joy Spark   +4 more
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Adverse reactions to isotretinoin. A report from the Adverse Drug Reaction Reporting System.

Journal of the American Academy of Dermatology, 1988
Between October 1982 and June 1985 the Adverse Drug Reaction Reporting System received reports of 104 suspected adverse reactions occurring in 93 patients who took isotretinoin. Adverse reactions involving the skin and mucous membranes (29 reports), central nervous system (23), musculoskeletal system (12), pregnancy (11), and eyes (8) were most ...
M, Bigby, R S, Stern
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Adverse drug reaction reporting: a working system.

Hospital pharmacy, 1987
Adverse drug reactions (ADRs) are a severe problem. Up to 30% of hospitalized medical patients may have an ADR, and up to 5% of hospitalizations may be caused by an ADR. Reporting systems that track these reactions vary widely as to their capture rates. In a 12-month period, with the aid of the Medical Record Department at St.
P A, Michelson, K, Shields
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Systemic Barriers and Potential Concerns from Reporting Serious Adverse Drug Reactions

2022
About 1-10% of all serious adverse drug reactions (sADRs) are reported to the Food and Drug Administration (FDA) ( Moore T, Bennett C. Underreporting of Hemorrhagic and Thrombotic Complications of Pharmaceuticals to the U.S. Food and Drug Administration: Empirical Findings for Warfarin, Clopidogrel, Ticlopidine, and Thalidomide from the Southern ...
Matthew A, Taylor, Ashley C, Godwin, Shamia, Hoque, Charles L, Bennett   +3 more
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Evaluation of adverse drug reaction reporting systems

2013
In July 1979, in accordance with the Joint Commission on Accreditation of Hospitals (JCAH) standards, the Pharmacy and Therapeutics Committee approved a policy for reporting adverse drug reactions (ADRs) occurring within the 370-bed University of Utah Hospital. This policy was intended "to provide a mechanism to accurately and completely report adverse
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Multiple sclerosis as an adverse drug reaction: clues from the FDA Adverse Event Reporting System

Expert Opinion on Drug Safety, 2018
Possible relationship between drug exposure and multiple sclerosis (MS) development is insufficiently investigated, and further challenged by the incomplete understanding of MS etiopathogenesis. The study aims to investigate whether drug exposure could contribute to MS, by analyzing worldwide spontaneous reporting archives of adverse drug reaction ...
Antonazzo, Ippazio Cosimo, Raschi, Emanuel, Forcesi, Emanuele, Riise, Trond, Bjornevik, Kjetil, Baldin, Elisa, De Ponti, Fabrizio, Poluzzi, Elisabetta   +7 more
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Physicians' knowledge and attitudes regarding the spontaneous reporting system for adverse drug reactions

Journal of Clinical Epidemiology, 2002
The spontaneous reporting system (srs) is the most important early warning system of adverse drug reactions. As there is serious under-reporting we studied the respective knowledge and attitudes of two samples of physicians in Germany. Five hundred randomly sampled physicians and 815 physicians who had actually reported an ADR were included; the ...
J, Hasford, M, Goettler, K-H, Munter, B, Müller-Oerlinghausen   +3 more
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Efficacy of reporting systems of adverse reactions to drugs and care.

Scandinavian journal of social medicine, 1984
Only 13% of adverse drug reactions that should have been reported to the Committee on Side Effects in Sweden according to the criteria published by the National Board of Health and Welfare, were actually reported by the responsible doctors. This was found in a prospective study of all adverse reactions established in 1 271 patients at a department of ...
C, Jorup-Rönström, S, Britton
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Adverse Reactions to Anticoagulants and to Antiplatelet Drugs Recorded by the German Spontaneous Reporting System

Seminars in Thrombosis and Hemostasis, 2005
According to their code of professional conduct, German physicians are obliged to report suspected cases of adverse drug reactions (ADRs) to the Drug Commission of the German Medical Association (AkdA). On the basis of an agreement between the German Medical Association and the Federal Institute for Drugs and Medical Devices (BfArM) a common ...
Jörg David, Tiaden, Ernst, Wenzel, Heiner K, Berthold, Bruno, Müller-Oerlinghausen   +3 more
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