The most common treatment-emergent adverse events were headache, indigestion and back pain

Data also showed that no new safety signals were observed with repeat dosing and the types of adverse events were consistent with those reported in earlier studies

The drug was also well tolerated, with similar rates of occurrence of serious adverse events among drug and placebo groups...There were no product-related serious adverse events in either arm

In addition, statistically significant increases in non-fatal serious adverse events (SAE) were observed in patients on Tredaptive plus statin therapy compared to placebo plus statin therapy...Adverse events were consistent with those already known for eplerenone, primarily hyperkalemia

The rate of serious adverse events and the rate of discontinuations due to adverse events were similar between the two groups

Adverse events reported in the study were generally mild or moderate in nature and similar in both placebo and treatment groups

Adverse events were mild, predictable and manageable...VX-787 was generally well tolerated, with no adverse events leading to discontinuation

Adverse event (AE) profiles were similar between the two treatment groups and consistent with known AEs associated with progesterone

The committee reviewed the treatment effect at one year on the primary outcome measure of efficacy, change in motor function using the MFM scale, together with the latest safety report, including electrocardiogram traces, periodic laboratory findings, hemostatic parameters and serious adverse events listings for all participants

However, preliminary safety data analyses suggested the benefit/risk ratio might not favor the trabedersen treatment arm due to serious adverse events associated with the local mode of administration, so the company will focus on systemic intravenous administration of trabedersen in glioma...The trial reported no imbalance in serious adverse events, and there were a low number of major adverse cardiovascular events

The adverse event profile was consistent with that known for Lyrica, with the most common adverse events including headache, dizziness, insomnia, somnolence, nausea and fatigue

The primary objectives include the evaluation of adverse events and the evaluation of six-month clinical response...The drug was well tolerated, with no significant differences in adverse events between the trial arms

Results showed no confirmed VTEs, and the rate of adverse events was similar to those found in pregnant patients during and immediately after delivery...There were also no adverse events among neonates

The most commonly reported adverse events were anorexia and fatigue

No serious adverse events or safety concerns were identified

The most common adverse events reported in the double-blind, placebo-controlled IMPRESS trials were hematoma, pain and swelling at the treatment site

A similar incidence of grade 3 or higher adverse events was seen in both arms of the trial (28 percent placebo; 27 percent Neulasta

There were no significant differences in the adverse event profiles between the three groups

Preliminary results from the 249-patient study indicated no unexpected adverse events and a favorable tolerability profile...No significant adverse events related to the drug occurred, and Nymox said NX-1207 treatment for BPH was not associated with the sexual, cardiovascular or other side effects associated with approved BPH medications