Adverse reactions to contrast media: An analysis from spontaneous reporting data

2007 ◽  
Vol 56 (1) ◽  
pp. 35-41 ◽  
Author(s):  
P CUTRONEO ◽  
G POLIMENI ◽  
R CURCURUTO ◽  
G CALAPAI ◽  
A CAPUTI
Author(s):  
Valeria Dipasquale ◽  
Giuseppe Cicala ◽  
Francesca Laganà ◽  
Paola Cutroneo ◽  
Patrizia Felicetti ◽  
...  

2019 ◽  
Vol 14 (2) ◽  
pp. 122-126
Author(s):  
Deepti Chopra ◽  
Abhinav Jain ◽  
Richa Garg ◽  
Shreya Dhingra

Background: Radiocontrast media are used extensively nowadays to visualize internal organs. Currently, non-ionic iodinated contrast media are used which are generally considered to be safe but some adverse reactions have been reported. Thus, the present study was carried out to analyze the nature and incidence of adverse drug reactions (ADRs) to radiographic contrast media in a teaching hospital. Methods:An observational study carried out for a period of six months in a teaching hospital. Contrast media induced adverse reactions were analyzed in terms of affected organs, rate, causality assessment, severity and preventability. The treatment and outcomes of adverse events were also recorded. Naranjo Probability Scale was used to evaluate the relationship between the contrast agent used and the suspected ADR. The severity of the suspected ADRs was determined using Hartwig Scale and preventability was assessed using modified Schumock and Thornton criterion. Results:A total of 15 suspected ADRs occurred in 11 patients with an incidence of 1.4%. It included 5 (45.4%) males and 6 (54.5%) females (p < 05). The highest percentage (72.7 %) of ADRs was seen in adult patients, the mean age being 40.8 years. Vomiting (33.3%) was the most common ADR noted followed by severe nausea and rashes. 64.7 % of ADRs were categorized as probable and 35.3 % were possible. Adverse reactions required treatment in 46.6% patients. There was no fatality reported. Conclusion:The reactions observed were mild to moderate in severity and occurred within 30 minutes of the administration of the contrast.


2021 ◽  
Vol 9 (5) ◽  
pp. e002521
Author(s):  
Sean Hammond ◽  
Anna Olsson-Brown ◽  
Joshua Gardner ◽  
Paul Thomson ◽  
Serat-E Ali ◽  
...  

Many adverse reactions associated with immune checkpoint inhibitor (ICI) treatments are immunologically driven and may necessitate discontinuation of the ICI. Herein, we present a patient who had been administered the radio contrast media amidotrizoate multiple times without issue but who then developed a Stevens-Johnson syndrome reaction after coadministration of atezolizumab. Causality was confirmed by a positive re-challenge with amidotrizoate and laboratory investigations that implicated T cells. Importantly, the introduction of atezolizumab appears to have altered the immunologic response to amidotrizoate in terms of the tolerance–elicitation continuum. Proof of concept studies demonstrated enhancement of recall responses to a surrogate antigen panel following in-vitro (healthy donors) and in-vivo (ICI patients) administrations of ICIs. Our findings highlight the importance of considering all concomitant medications in patients on ICIs who develop immune-mediated adverse reactions. In the event of some immune-related adverse reactions, it may be critical to identify the culprit antigen-forming entity that the ICIs have altered the perception of rather than simply attribute causality to the ICI itself in order to optimize both patient safety and treatment of malignancies.


2012 ◽  
Vol 24 (1) ◽  
pp. 22 ◽  
Author(s):  
Kyung Eun Jung ◽  
Jimin Chung ◽  
Byung Cheol Park ◽  
Keum Nahn Jee ◽  
Young Koo Jee ◽  
...  

2001 ◽  
Vol 176 (6) ◽  
pp. 1389-1392 ◽  
Author(s):  
Kelly S. Freed ◽  
Richard A. Leder ◽  
Cindy Alexander ◽  
David M. DeLong ◽  
Mark A. Kliewer

1992 ◽  
Vol 19 (5) ◽  
pp. 899-906 ◽  
Author(s):  
Edward W. Gertz ◽  
Judith A. Wisneski ◽  
Robert Miller ◽  
Merrill Knudtson ◽  
John Robb ◽  
...  

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