Examples of using Package leaflets in English and their translations into Romanian
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Programming
Information on the label and package leaflets;
Read the package leaflets for these medicines for their dosage and directions on‘how to take' them.
Furthermore, it is important that you carefully read the package leaflets that are provided with these medicines.
Ask your doctor if you are unsure about any contraindications mentioned in the package leaflets.
It is therefore very important that you read the package leaflets that are provided with these medicines.
Read the package leaflets for these other medicines for information regarding driving and using machines.
If you are unsure of any information in the package leaflets, please contact your doctor or pharmacist.
Please read the package leaflets for the other medicines that are part of your treatment, to see if they are suitable for you.
For more information on the side effects of atazanavir ordarunavir see the package leaflets for these medicines.
It is very important that you also read the package leaflets for the other antiviral medicines that you take with Exviera.
Pharmacovigilance was a first success,with the adoption of drug safety portals that included the package leaflets and information on the medicines.
Read the package leaflets for the other medicines used for treating your hepatitis C infection for side effects reported with these medicines.
As Ongentys will be used with other levodopa medicines,please also read the package leaflets of these medicines carefully.
The documents approved by the consent authorities(package leaflets and summary of product characteristics) contain important information about the product.
Information on restrictions that apply specifically to medicines radiolabelled with Lumark will be found in the package leaflets of those medicines.
In addition, drug licensing authorities have allowed the inclusion in package leaflets of codes(QR codes) that link to package leaflets on the company website.
Information on restrictions that apply specifically to medicines radiolabelled with EndolucinBeta can be found in the package leaflets of those medicines.
In Italy, pharmacies are required by law to print out updated package leaflets that the pharmaceutical industry has put on a database.
When Daklinza is used together with peginterferon alfa andribavirin the reported side effects are the same as those listed in the package leaflets for these medicines.
You must read the package leaflets of all medicinal products to be taken in combination with Neofordex for information related to these medicines before starting treatment with Neofordex.
In order to cover themselves, pharmaceutical companies often include every minor side effect in package leaflets, which, of course, complicates matters greatly.
The general public shall have access to information in the product database as regards the list of the authorised veterinary medicinal products,their summaries of product characteristics and package leaflets.
It is also important for information tobe accessible via other channels, in addition to package leaflets, and I therefore welcome publication on the Internet.
The EESC proposed that the package leaflets of the pharmaceutical products contain information in a simple and direct visual form based on three colours: benefits(green band), contraindications(yellow band), and possible risks(red band).
The CHMP, in the light of the data submitted and the scientific discussion within the Committee,was of the opinion that the SPCs, labelling and package leaflets should be harmonised across the EU.
Scientific conclusions andgrounds for amendment of the summaries of product characteristics and package leaflets presented by the emea overall summary of the scientific evaluation of piroxicam containing medicinal products(see annex i).
Since Daklinza must always be used in combination with other medicines against hepatitis C infection,please make sure that you read the"Do not take" section of the package leaflets for these medicines.
Does Article 69 of Directive 2001/83/EC 1 make exhaustive provision with respect to the permissible content of package leaflets for the medicinal products referred to in Article 14(1) or may other information within the meaning of Article 62 of Directive 2001/83/EC be included?
(a) veterinary medicinal products authorised within the Union by the Commission and by the competent authorities,together with their summaries of product characteristics, package leaflets and lists of sites where each product is manufactured;
The competent authorities may exempt labels and package leaflets for specific medicinal products from the obligation that certain particulars shall appear and that the leaflet must be in the official language or languages of the Member State where the product is placed on the market, when the product is not intended to be delivered to the patient for self-administration.