Примери за използване на Restricted indication на Английски и техните преводи на Български
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The benefits and risks of Xofigo in the restricted indication should also be further characterised.
After re-examination, the CHMP granted a positive opinion for a restricted indication i.e.
This proposal for a restricted indication is in line with the current EU treatment guidelines to not overall recommend fluoroquinolones as first line treatment option.
The CHMP also discussed whether a conditional Marketing Authorisation for the claimed restricted indication could be considered.
In the 19 clinical studies that are argued to be supportive of this restricted indication, and which included heterogeneous populations, some did not show significant effects of dihydroergotoxine.
The CHMP reviewed all available data in support of the benefit andsafety on dihydroergotoxine and considered the above restricted indication proposed by the MAH.
Instead, the more restricted indication in complicated UTI and pyelonephritis was proposed, in line with other recently harmonised products as well as in compliance with clinical practice.
In view of the unpredictability of this type of adverse reactions, a restricted indication would not be an effective risk minimisation measure.
The CHMP concluded that the benefit/ risk balance of systemic formulations of piroxicam containing medicinal products in the agreed restricted indications is favourable.
Although most studies were outdated and/or of poor quality,the CHMP was of the opinion that a restricted indication would be justified and in conclusion, adopted the following harmonised indication: .
Restricted indication in the intermittent treatment of moderate to severe symptoms of uterine fibroids in adult women of reproductive age: Esmya should only be used in women who are not eligible for surgical treatment.
The CHMP concluded that the benefit/ risk balance of bicalutamide 150 mg containing medicinal products in the agreed restricted indication is favourable.
One of the proposed further risk minimisation measures by the MAH was a restricted indication in patients with PaO2 between 55 mmHg and 65 mmHg or as adjuvant treatment to Long Term Oxygen Therapy(LTOT).
The PRAC considered that the risk minimisations measuresdiscussed during the assessment, including reduction of duration of treatment and restricted indication, were not sufficient to reduce the risk.
The experts were asked to discuss any restricted indication where the benefit/risk could be regarded as positive in the current armamentarium, and particularly the restricted indication proposed by the MAH.
The CHMP also noted that no comparative, placebo-controlled ordouble-blinded studies were available in the restricted indication severe ear, nose and throat-infections.
In the opinion of the CHMP, the proposed restricted indication clearly describes a fairly small patient population who cannot profit from the superior recently introduced regimens MPT(melphalan, prednisone and thalidomide) or MTV(melphalan, topotecan and VP-16 phosphate), including thalidomide or bortezomib.
The PRAC considered risk minimisations measures,including reduction of duration of treatment to 6 days and a restricted indication, to mitigate the risk of serious cutaneous adverse reactions.
The CHMP considered that none of the provided pooled analyses could be considered as supportive to demonstrate the efficacy of tolperisone in the“treatment of muscular hypertonicity and muscle spasms associated with locomotor diseases” indication, nor in the proposed restricted indication.
The PRAC considered that the risk minimisations measures discussed during the assessment,including reduction of duration of treatment and restricted indication, were not sufficient to reduce the risk of serious cutaneous reactions.
In view of the restricted indication and contraindication in patients with pre-existing hepatic disease or hepatic impairment, the PRAC recommended that physicians should re-evaluate promptly whether daclizumab continues to be an appropriate treatment option for each of their patients currently treated with this medicinal product, taking into account the provisional measures recommended by the PRAC.
The scope of the re-examination focused on the re-evaluation of the benefit-risk balance of dihydroergotoxine in the restricted indication proposed by the MAH which is“symptomatic treatment of cognitive impairment in elderly, excluding Alzheimer's disease and dementia”.
Based on the totality of the data made available on the safety and the efficacy of tolperisone, the CHMP considered that the risk of hypersensitivity is more significant than previously identified, andthat as a consequence the demonstrated clinical benefits only outweigh the risks in the restricted indication symptomatic treatment of post-stroke spasticity in adults.
The PRAC endorsed a Direct Healthcare Professional Communication(DHPC), to communicate the outcome of the present review to the healthcare professionals,in particular, the restricted indication and maximum duration of use and to highlight the risk of hepatotoxicity and the necessary measures needed to minimise this risk.
Study to address all important, potential andidentified risks, particularly Parkinsonism and a drug utilization study to verify the compliance of prescribers regarding the restricted indication after marketing authorisation changes was also agreed.
Overall, based on the assessment of the detailed grounds for re-examination submitted by the applicant, including the revised risk management proposals for monitoring of liver lipids andliver toxicity, and the revised restricted indication, as applied for by the applicant, the CHMP concluded that the benefit/risk of Kynamro remains unfavourable.
A drug utilisation study(DUS) in order to verify the comprehension of the indication, the awareness of the safety concern, the minimisation measures in the SmPC in term of restriction of indication, the new caution related use of the product at different time(e.g. when the restricted indication is implemented/ 6 months after the implementation/ 18 months after the implementation).
The absence of reliable effects data for plants and microorganisms means that reducing exposure,i.e. lowering the PECsoil by restricting indications and species does not alter the potential for an unacceptable risk.
The CHMP restricted the indication for a number of medicines for efficacy or safety reasons, including.
The indication is restricted to enteric infections caused by non-invasive E. coli susceptible to colistin.