Sentences with phrase «adverse events study»

The authors of the 2004 Canadian Adverse Events Study, which examined the incidence of adverse events among hospital patients coast to coast, estimated that between 3,561 and 9,143 patients in Ontario died as a result of nearly 72,000 adverse medical events.

[1] G. Ross Baker et al, The Canadian Adverse Events Study: the incidence of adverse events among hospital patients in Canada, CMAJ May 25, 2004 vol.

Not exact matches

Through week 48, Biktarvy was found to be statistically non-inferior to ABC / DTG / 3TC with a numerically lower incidence of mild or moderate study drug - related adverse events and no treatment - emergent resistance;

Tough summarizes key research, such as the Adverse Childhood Experience Study, a project of the Centers for Disease Control and Kaiser Permanente, which revealed a stunning correlation between traumatic childhood events and negative adult outcomes.

Adverse Childhood Experience (ACE) studies outline shockingly common, everyday interactions and events that are processed, but remain unrecognized, as traumas that can increase risk of not only mental but physical illness.

In a letter to Martek FDA said: «some studies have reported adverse events and other morbidities including diarrhea, flatulence, jaundice and apnea in infants fed long - chain polyunsaturated fatty acids.»

The study, published 13 June 2013, focused on two serious adverse events: postpartum hemorrhage and manual removal of the placenta, both of which are life - threatening, and also included admission to intensive care, eclampsia, and more than four packed cells in a blood transfusion.

Breastfeeding was more effective in reducing crying duration or pain scores during vaccination compared to: 25 % dextrose and topical anaesthetic cream (EMLA), vapocoolant, maternal cuddling, and massage.No included studies reported adverse events.

One important point for me is that there were no adverse events (scientific - speak for bad side effects) reported in either the 2010 study or the 2014 study.

A 10 - year study finds that people who experienced adverse childhood events also lose years off their lives

In the study, patients who underwent conscious sedation had a similar rate of adverse events to those who underwent anesthesia, but those who were given conscious sedation had shorter stays in the intensive care unit (30 versus 96 hours for those with general anesthesia) and shorter hospital stays (4.9 days versus 10.4 days).

During the study period, the incidence of serious adverse events was no higher among those receiving inosine than among the placebo group.

The study shows those apparently healthy individuals identified with increased carotid plaque burden and coronary artery calcium were two to three times more likely to have an adverse event such as an artery blockage, or a piece of plaque becoming loose causing a heart attack or stroke.

In fact, after follow - up (2.5 to 3.1 years), there were a total of 216 adverse events reported among study participants including 108 deaths, of which 27 were cardiovascular, plus 34 heart attacks, 30 strokes, 18 experienced unstable angina and hospitalized, and 79 needed revascularization procedures.

Eight adverse events were reported during the study, most were due to pain at the injection site.

For lutein, studies showed efficacy and that the only adverse event that's been shown is non-life threatening yellowing of skin.

The results of this study highlight the importance of the guidelines to avoid adverse events associated with benzodiazepine and related drug use.

Nearly a quarter (24.1 %) of all adverse events were judged to be unrelated to the study drug, and the vast majority (84.6 %) of adverse events were classified as mild, 14.4 % as moderate, and 1 % as severe.

Overall, there were three serious adverse events for every 1,000 participants, with several occurring in subjects receiving placebos and others judged unrelated to the study drug or a study procedure.

Nearly 20 % of the adverse events occurred on the first day of the study.

Nine patients experienced serious adverse events three of which were considered related to treatment, the study states.

The study results show that with a median (midpoint) follow - up of 20 months, 232 patients (75 percent) remained on therapy, 31 (10 percent) discontinued because of disease progression and 45 discontinued for other reasons (including 28 because of infection, eight for other adverse events and nine due to other medical events).

Third, it is not in the interest of the pharmaceutical company to minimize recording of adverse events since determinations must be made about whether to conduct additional expensive clinical studies.

Patients with multiple health issues and who are at higher risk of adverse events are less likely to receive follow - up care from a physician after visiting an emergency department for chest pain, reports a study published in CMAJ (Canadian Medical Association Journal)

With a total of 143 (36 %) studies involving placebo, 10.3 % of all adverse events (2,528) occurred in participants receiving placebo.

In the largest study of its kind, researchers found only 34 (0.31 %) healthy volunteers with serious adverse events, which are defined by the FDA as those that result in death; are life - threatening; require or prolong in - patient hospitalization; or cause a disability, congenital anomaly or birth defect.

Less than 1 % of patients in the studies discontinued treatment due to treatment - emergent adverse events.

In the RBV - containing arms of the ION studies, the most common adverse events were fatigue, headache, nausea and insomnia.

Another study on this device will be presented on Monday and will review the initial results of a 30 subject study, adverse events post-implant, system reliability and visual function results.

Fewer adverse events were observed in the RBV - free, fixed - dose combination arms compared to the RBV - containing arms in all the ION studies.

There was no significant increase in adverse events with any of the treatments over the control group, nor was there any difference in malaria incidence between groups during the one year period after the study treatment was stopped, suggesting that monthly administration of DP is a safe and effective treatment for reducing malaria among infants in regions with year - round transmission and high resistance to antifolates.

A new study published by the scientific journal Addiction found that take - home naloxone programs reduce overdose mortality and have a low rate of adverse events.

This study should inform those who restrict their view of causes for adverse effects to only postnatal environments and events.

Over the 19 years of the study, 1800 adverse cardiac events occurred, including heart attack, stroke or death due to heart disease or stroke.

Adverse events potentially related to the study included kidney stones (16 participants in the treatment group and 10 in the placebo group) and elevated serum calcium levels (six in the treatment group and two in the placebo group).

The type and duration of sun exposure, number and severity of phototoxic reactions, and adverse events were recorded over the study periods.

In a retrospective, multicenter, longitudinal observational study, the response rates to fecal microbiota transplantation as a treatment for recurrent C. difficile infection were determined a 30 and 90 days, and adverse events were registered.

The study, presented at The International Liver Congress ™ 2017 in Amsterdam, The Netherlands, also showed that the fixed - dose combination of LDV / SOF was well - tolerated, and no patients experienced a serious adverse event considered related to the study drug.

All adverse events were either mild or moderate in severity; there were no serious adverse events in the study.

The study authors conclude that physicians must weigh risks of adverse events «against the uncertain benefits» of combing mitral - valve repair during CABG.

The study team found a significantly higher risk of adverse events for broad - spectrum antibiotics compared to narrow - spectrum antibiotics (3.7 percent vs. 2.7 percent as documented by clinicians, and 35.6 percent vs. 25.1 percent, as reported by patients and families).

No children discontinued the study due to side effects or had a severe or life - threatening adverse event related to the study drug.

«Although previous studies of non-surgical weight loss interventions failed to show consistent results regarding asthma risks, our result strongly suggests that the kind of significant weight loss that often results from bariatric surgery can reduce adverse asthma events.»

A two - drug antihypertensive treatment that included a beta - blocker was associated with increased risk for major adverse cardiovascular events (MACEs) and death in a study of Danish patients who underwent noncardiac surgery, according to an article published online by JAMA Internal Medicine.

Limitations of the study include that causality of adverse events can not be determined from the data, health outcomes are self - reported and reports from consumers vs. health care professionals can not be distinguished.

But the work ground to a halt in 2000 after a volunteer in one of Hayden's studies experienced what FDA calls an «adverse event.»

As part of the approval, the manufacturer must conduct a five year post approval study that will follow at least 100 patients and collect additional safety and effectiveness data including weight loss, adverse events, surgical revisions and explants and changes in obesity - related conditions.

The 28 recorded adverse events that led to an interruption in PrEP included nausea and headache, but there were no serious adverse events deemed related to study drug.

Patients with uncontrolled high blood pressure treated with renal denervation had low rates of adverse events and significant lowering of blood pressure at six months, according to a registry - based study presented at the American College of Cardiology's 63rd Annual Scientific Session.

Serious adverse events reported in the clinical study included nausea, pain at the neuroregulator site, vomiting, as well as surgical complications.