| Human medicinal products | | | SPC PL |  | Veterinary medicinal
products | | SPC PL | | | Herbal medicinal products | | | SPC PL | | Name of the medicinal
product |
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Package Leaflets (PL) for Human medicinal products
The package leaflet (PL) provides users with information about the medicinal product and its correct use. The package leaflets contain instructions in both Finnish and Swedish.
The package leaflets can be searched from alphabetical list, with the name, marketing authorisation number and the Anatomical Therapeutic Chemical, i.e. ATC Code of the Summary of Product Characteristics, SPC.
The package leaflets processed as part of the EU centralised marketing authorisation procedure are published by the European Medicines Agency, EMA.
Fimea's service contains links to the documents on medicinal products (EPAR PI) on the EMA website.
Drugs belonging to the centralised authorisation procedure can be searched in Fimea's service by using an alphabetical list or by entering the product name or ATC code.
The material being published is not necessarily complete or up-to-date due to the technical quality of files submitted to the Finnish Medicines Agency Fimea or earlier to the National Agency for Medicines and the delays in delivery. For this reason, Fimea cannot guarantee that the document on the Internet fully complies with the summary of product characteristics and package leaflet officially approved by a desicion for a marketing authorisation. Only the hard copies of the SPCs and the PLs, which are in accordance with the marketing authorisation, are conclusive.
| Product Information Leaflets 181 - 210 of 255 |
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| SPC | Status for
supply | Name of the medicinal product |
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SPC
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Resepti
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Rivaxa 15 mg ja 20 mg tabletti, kalvopäällysteinen pakkausseloste 2024-06-21
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SPC
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Resepti
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Rivaxa 2,5 mg tabletti, kalvopäällysteinen pakkausseloste 2024-03-15.docx
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European Medicines Agency's website:
Rixathon - EMA: EPAR PI
Finnish Swedish
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European Medicines Agency's website:
Riximyo - EMA: EPAR PI
Finnish Swedish
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European Medicines Agency's website:
Riximyo - EMA: EPAR PI
Finnish Swedish
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European Medicines Agency's website:
Rixubis - EMA: EPAR PI
Finnish Swedish
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SPC
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Resepti
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Rizastad 10 mg tabletti, suussa hajoava PL 2024-04-12
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SPC
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Resepti
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Rizatriptan Stada 10 mg tabletti PL 2024-04-11
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European Medicines Agency's website:
Rizmoic - EMA: EPAR PI
Finnish Swedish
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European Medicines Agency's website:
RoActemra - EMA: EPAR PI
Finnish Swedish
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SPC
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Resepti
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Robinul 0,2 mg-ml injektioneste, liuos PL 2021-10-01
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SPC
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Resepti
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Robinul-Neostigmin 0.5 mg-ml + 2.5 mg-ml injektioneste, liuos PL 2021-11-30
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SPC
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Resepti
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Rocephalin cum lidocain 1 g injektiokuiva-aine ja liuotin, liuosta varten PL 2024-08-21
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European Medicines Agency's website:
Roclanda - EMA: EPAR PI
Finnish Swedish
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European Medicines Agency's website:
Roctavian - EMA: EPAR PI
Finnish Swedish
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SPC
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Resepti
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Rocuronium B.Braun 10 mg-ml injektio-infuusioneste, liuos PL 2024-03-22
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SPC
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Resepti
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Rocuronium bromide Aguettant 10 mg-ml injektioneste, liuos, esitäytetty ruisku pakkausseloste 2023-07-28.docx
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SPC
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Resepti
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Rocuronium Fresenius Kabi 10 mg-ml injektio - infuusioneste, liuos PL 2024-01-26
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SPC
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Resepti
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Rocuronium hameln 10 mg - ml injektio - infuusioneste, liuos PL 2023-12-05
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SPC
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Itsehoito
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Rogaine 50 mg-ml liuos iholle PIL 2022-10-03
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European Medicines Agency's website:
Rolufta Ellipta - EMA: EPAR PI
Finnish Swedish
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SPC
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Itsehoito
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Rometor ratiopharm 2 mg-ml oraaliliuos PL 2022-10-04
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European Medicines Agency's website:
Ronapreve - EMA: EPAR PI
Finnish Swedish
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SPC
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Resepti
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Ropinirol krka 2 mg, 4 mg, 8 mg, depottabletti PL 2023-05-29
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SPC
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Resepti
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Ropinirol Orion 2 mg, 4 mg, 8 mg depottabletti PL 2023-12-27
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SPC
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Resepti
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Ropinostad 2 mg, 4 mg, 8 mg depottabletti PL 2023-05-30
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SPC
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Resepti
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Ropivacain Fresenius Kabi 2 mg-ml infuusioneste, liuos PL 2024-02-29
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SPC
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Resepti
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Ropivacain Fresenius Kabi 2 mg-ml, 7.5 mg-ml, 10 mg-ml injektioneste, liuos PL 2024-02-22
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SPC
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Resepti
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Ropivacain Fresenius Kabi 5 mg-ml injektioneste, liuos PL 2024-02-22
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SPC
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Resepti
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Ropivacaine BioQ 2 mg/ml infuusioneste, liuos, antovälineistö, PL 2024-01-29
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