Reporting Rates of Yellow Fever Vaccine 17D or 17DD-Associated Serious Adverse Events in Pharmacovigilance Data Bases: Systematic Review

2011 ◽  
Vol 6 (3) ◽  
pp. 145-154 ◽  
Author(s):  
Roger E. Thomas ◽  
Diane L. Lorenzetti ◽  
Wendy Spragins ◽  
Dave Jackson ◽  
Tyler Williamson
Vaccine ◽  
2011 ◽  
Vol 29 (28) ◽  
pp. 4544-4555 ◽  
Author(s):  
Roger E. Thomas ◽  
Diane L. Lorenzetti ◽  
Wendy Spragins ◽  
Dave Jackson ◽  
Tyler Williamson

Vaccine ◽  
2005 ◽  
Vol 23 (25) ◽  
pp. 3256-3263 ◽  
Author(s):  
Alena Y. Khromava ◽  
Rachel Barwick Eidex ◽  
Leisa H. Weld ◽  
Katrin S. Kohl ◽  
Robert D. Bradshaw ◽  
...  

Vaccines ◽  
2020 ◽  
Vol 8 (2) ◽  
pp. 249 ◽  
Author(s):  
Cristina Domingo ◽  
Judith Lamerz ◽  
Daniel Cadar ◽  
Marija Stojkovic ◽  
Philip Eisermann ◽  
...  

Background: The yellow fever (YF) vaccination is recommended by the WHO for people traveling or living in endemic areas at risk for yellow fever infections in Africa and South America. Although the live attenuated yellow fever vaccine is a safe and efficient vaccine, rare serious adverse events after vaccination have been reported. Case presentation: We present the case of a 74-year-old male with multiorgan failure after yellow fever vaccination for a trip to Brazil. The patient required admission to the intensive care unit with a prolonged stay due to severe organ dysfunction. Five days after the YF vaccination, the patient experienced nausea, vomiting, diarrhea, and general illness. Three days later he sought medical attention and was transferred to the University Hospital Heidelberg with beginning multiorgan failure and severe septic shock, including hypotonia, tachypnea, thrombopenia, and acute renal failure the same day. Within one week after vaccination, antibodies against YF virus were already detectable and progressively increased over the next two weeks. Viral RNA was detected in serum on the day of admission, with a viral load of 1.0 × 105 copies/mL. The YF virus (YFV) RNA was also present in tracheal secretions for several weeks and could be detected in urine samples up to 20 weeks after vaccination, with a peak viral load of 1.3 × 106 copies/mL. After 20 weeks in the ICU with nine weeks of mechanical ventilation, the patient was transferred to another hospital for further recovery. Conclusions: The risk for severe adverse events due to the YF vaccination should be balanced against the risk of acquiring a severe YF infection, especially in elderly travelers.


2015 ◽  
Vol 11 (9) ◽  
pp. 2183-2187 ◽  
Author(s):  
Reinaldo de Menezes Martins ◽  
Maria da Luz Fernandes Leal ◽  
Akira Homma

2021 ◽  
Vol 10 (1) ◽  
Author(s):  
Sophie Juul ◽  
Faiza Siddiqui ◽  
Marija Barbateskovic ◽  
Caroline Kamp Jørgensen ◽  
Michael Pascal Hengartner ◽  
...  

Abstract Background Major depressive disorder is one of the most common, burdensome, and costly psychiatric disorders worldwide. Antidepressants are frequently used to treat major depressive disorder. It has been shown repeatedly that antidepressants seem to reduce depressive symptoms with a statistically significant effect, but the clinical importance of the effect sizes seems questionable. Both beneficial and harmful effects of antidepressants have not previously been sufficiently assessed. The main objective of this review will be to evaluate the beneficial and harmful effects of antidepressants versus placebo, ‘active placebo’, or no intervention for adults with major depressive disorder. Methods/design A systematic review with meta-analysis will be reported as recommended by Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA), bias will be assessed with the Cochrane Risk of Bias tool-version 2 (ROB2), our eight-step procedure will be used to assess if the thresholds for clinical significance are crossed, Trial Sequential Analysis will be conducted to control for random errors, and the certainty of the evidence will be assessed with the Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach. To identify relevant trials, we will search both for published and unpublished trials in major medical databases from their inception to the present. Clinical study reports will be obtained from regulatory authorities and pharmaceutical companies. Two review authors will independently screen the results of the literature searches, extract data, and perform risk of bias assessment. We will include any published or unpublished randomised clinical trial comparing one or more antidepressants with placebo, ‘active placebo’, or no intervention for adults with major depressive disorder. The following active agents will be included: agomelatine, amineptine, amitriptyline, bupropion, butriptyline, cianopramine, citalopram, clomipramine, dapoxetine, demexiptiline, desipramine, desvenlafaxine, dibenzepin, dosulepin, dothiepin, doxepin, duloxetine, escitalopram, fluoxetine, fluvoxamine, imipramine, iprindole, levomilnacipran, lofepramine, maprotiline, melitracen, metapramine, milnacipran, mirtazapine, nefazodone, nortriptyline, noxiptiline, opipramol, paroxetine, protriptyline, quinupramine, reboxetine, sertraline, trazodone, tianeptine, trimipramine, venlafaxine, vilazodone, and vortioxetine. Primary outcomes will be depressive symptoms, serious adverse events, and quality of life. Secondary outcomes will be suicide or suicide attempt, suicidal ideation, and non-serious adverse events. Discussion As antidepressants are commonly used to treat major depressive disorder in adults, a systematic review evaluating their beneficial and harmful effects is urgently needed. This review will inform best practice in treatment and clinical research of this highly prevalent and burdensome disorder. Systematic review registration PROSPERO CRD42020220279


Author(s):  
Laura Ramos de Almeida ◽  
Roberta Fachini Criado ◽  
Paulo Ricardo Criado ◽  
Luis Felipe Ensina ◽  
Beatrice Martinez Zugaib Abdalla ◽  
...  

Vaccine ◽  
2008 ◽  
Vol 26 (43) ◽  
pp. 5441-5442 ◽  
Author(s):  
Alan D.T. Barrett ◽  
Matthias Niedrig ◽  
Dirk E. Teuwen

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