The phrase "adverse harm" is somewhat redundant but can be used in written English.
It is typically used in contexts discussing negative effects or consequences, particularly in legal, medical, or environmental discussions.
Example: "The study aimed to assess the potential for adverse harm resulting from the new chemical exposure."
Alternatives: "negative impact" or "detrimental effect".
An environmental impact study performed by NASA in 2007 similarly concluded that 30 years of astronomy had caused "significant, substantial and adverse" harm to Mauna Kea.
It said: "Insufficient evidence has been submitted or exists to prove that the proposal will directly impact and result in significant adverse harm to the economic well being of the local tourism sector.
The coordinated functions of these stress/defense-related proteins could protect grain development from adverse harm, and benefit wheat yield and quality.
PubMed© was searched using the keywords trigger tool, adverse event, harm, medical record, record review, reporting systems, pediatric, children, adult, safety management, inpatient and/or outpatient.
(diabetic macular edema or diabetic macular oedema or diabetic retinopathy or diabetic maculopathy).m_titl. 1 and 2 (risk or safety or adverse or harm or pharmacovigilance).tw.tw
Reasons for discontinuation of RCTs include unanticipated adverse effects (harm) [ 1], larger than expected benefit of an intervention (early superiority) [ 2], or a very low probability of detecting a designated treatment effect with continued patient recruitment or follow-up (futility) [ 3].
We define a 'discontinued RCT' as any RCT that was stopped before reaching at least 90% of the planned sample size due to any reason, including futility, adverse events (harm), early evidence of superiority of one intervention (benefit) and insufficient recruitment (a cut-off at 80% of the planned sample size will be considered in a sensitivity analysis).
Other measures of adherence, adverse events, harms, use of health services/co-interventions, and process measures including appropriateness and satisfaction of the intervention, will be collected at 3, 6 and 9 months.
No adverse events, harms, or unintended events were reported.
Other measures of adherence, adverse events, harms, use of health services/co-interventions, and process measures including appropriateness and satisfaction of the intervention, will be collected at 3, 6 and 9 months.
5 7 The standard CONSORT statement 8 is primarily aimed at reporting the intended, usually beneficial effects of intervention(s) with only one item (item 19) devoted to unintended adverse events (harms) in the original 2001 checklist.
