Примери за използване на Reported serious на Английски и техните преводи на Български
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There were no reported serious.
None of the reported serious events in Study 204 were considered to be possibly related to Fexeric.
Few patients with ADA reported serious/severe AEs.
Reported serious infections were similar to those seen in RA patients with the addition of varicella and otitis media.
Cerebral haemorrhage and gastrointestinal haemorrhage were the most commonly reported serious bleeding events.
The most commonly reported serious adverse reaction was cellulitis(1.1%).
An in depth assessment is needed to firmly establish factors that may have caused the reported serious hepatic injuries.
The most commonly reported serious adverse reaction was pneumonia(11.5%).
The most commonly reported infections were upper respiratory tract infection and pharyngitis, andthe most commonly reported serious infection was abscess.
Studies have not reported serious side effects related to CoQ10 use.
According to the new CDC paper, 8.7 percent of people with incomes below the poverty line, or$20,090 for a family of three, reported serious psychological distress from 2009 to 2013.
The most commonly reported serious infection in the rituximab group was mild or moderate bronchitis.
Vasovagal syncope represents a transient, self-limited loss of consciousness, from which subsequent recovery is spontaneous, complete, andusually prompt, without reported serious associated injury.
The most frequently reported serious adverse reaction was immune reconstitution syndrome and rash.
According to the Center for Disease Control and Prevention, 8.7 percent of people with incomes below the poverty line,which approximately rounds up to $20,000 for a family of three, reported serious psychological distress from 2009 to 2013.
The most frequently reported serious adverse reactions were immune reconstitution syndrome and rash.
Reported serious infections included pneumonia, cellulitis, herpes zoster, gastroenteritis, diverticulitis, sepsis and bacterial arthritis.
In the monotherapy studies, the most frequently reported serious adverse reactions(≥2%) were pneumonia and febrile neutropenia.
Reported serious infections, some with fatal outcome, included pneumonia, cellulitis, herpes zoster, gastroenteritis, diverticulitis, sepsis, bacterial arthritis.
It has been shown to be safe for patients with no reported serious side effects and it is considered to lack acute or chronic toxicity.
Reported serious infections, some with fatal outcome, included active tuberculosis, which may present with intrapulmonary or extrapulmonary disease, invasive pulmonary infections, including candidiasis, aspergillosis, coccidioidomycosis and pneumocystis jirovecii, pneumonia, cellulitis, herpes zoster, gastroenteritis, diverticulitis, sepsis and bacterial arthritis.
In clinical studies to date with alpha lipoic acid, there have been no reported serious adverse side effects, even at the high doses used to treat diabetics and patients suffering from neurodegenerative diseases.
Less frequently reported serious ocular adverse reactions included endophthalmitis, retinal haemorrhage, vitreous haemorrhage and retinal detachment.
In 2011, a French national pharmacovigilance review reported serious cases of valvulopathy, pulmonary, pleural and retroperitoneal fibrosis associated with methysergide containing medicinal products.
(54) The assessment of reported serious incidents and field safety corrective actions should be conducted at national level but where similar incidents have occurred or field safety corrective actions have to be carried out in more than one Member State coordination, with the objective of sharing resources and ensuring consistency regarding the corrective action, and transparency of procedures should be ensured.
The most frequently reported serious infection in the rituximab group was pneumonia at a frequency of 4%.
The most frequently reported serious adverse reactions were pneumonia, pyrexia, infusion related reaction and cellulitis.
The most frequently reported serious ADRs were decreased ejection fraction and congestive cardiac failure.
The most frequently reported serious related adverse events included nausea, vomiting, diarrhoea, pyrexia, and increased bilirubin.
More patients reported serious adverse events in the zoledronic acid group than in the placebo group(5[27.8%] patients versus 1[6.3%] patient).