Eksempler på bruk av Limited data are available på Engelsk og deres oversettelse til Norsk
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Limited data are available in elderly.
No significant differences in safety and efficacy of Perjeta were observed between elderly patients aged 65 to 75 years and adult patients aged< 65 years.No dose adjustment is necessary in the elderly population≥ 65 years of age. Very limited data are available in patients> 75 years of age.
Limited data are available in diabetic patients.
As only limited data are available the clinical significance is not known.
Limited data are available in patients with hepatic impairment.
Very limited data are available in patients> 75 years of age.
Limited data are available on the use of the Breelib nebuliser.
Limited data are available related to overdose in humans.
Limited data are available for co- administration with indinavir.
Limited data are available in patients< 1 year of age(see section 5.1).
Limited data are available on the elimination of temoporfin in humans.
Limited data are available for Selincro in the 1-month run-out period.
Only limited data are available for the use of Zalviso in such patients.
Limited data are available but no recommendation on a posology can be made.
Only limited data are available for the use of sufentanil in such patients.
Limited data are available in elderly people treated with higher doses of lurasidone.
Limited data are available on the safety and efficacy of Perjeta in patients≥ 65 years of age.
Limited data are available on patients with moderate(CLCR: 30 to 50 mL/min) renal impairment.
Limited data are available on the development of resistance to atazanavir boosted with cobicistat.
Limited data are available on the pharmacokinetics of indinavir in association with low dose ritonavir.
Limited data are available on the use of Xolair in combination with specific immunotherapy hypo-sensitisation therapy.
Limited data are available on the effects of the highly potent alpha-2- agonists(medetomidine and romifidine) as premedication.
Limited data are available for reversal of pancuronium induced blockade, but it is advised not to use sugammadex in this situation.
Limited data are available from an ongoing follow-up study to assess durability of response up to 3 years after treatment with daclatasvir.
Since only limited data are available for patients with moderate hepatic impairment(Child Pugh B), no dose recommendation can be provided.
Only very limited data are available from repeat-dose toxicity studies with respect to the risk for adverse effects on the male reproductive system.
Limited data are available on the combined use of Ferriprox and deferasirox, and caution should be applied when considering the use of such combination.
Although only limited data are available, there is no obvious effect of race, height, weight, gender or age on CSF ziconotide exposure after IT administration.
Limited data are available in patients with severe renal insufficiency(creatinine clearance< 30 ml/min) and therefore rosiglitazone should be used with caution in these patients.
Only limited data are available for patients carrying the G551D-CFTR mutation with percent predicted FEV1(forced expiratory volume exhaled in the first second) of less than 40% 12 patients.