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 151 - 180 of 257 |
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SPC | Status for supply | Name of the medicinal product |
SPC
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Resepti
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Bonjesta 20 mg - 20 mg säädellysti vapauttava tabletti PL 2023-05-26
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SPC
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Resepti
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Bonoq Uro 200 mg tabletti PIL 2002-08-26
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SPC
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Resepti
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Bonoq Uro 400 mg tabletti PIL 2002-08-26
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European Medicines Agency's website: Bonviva - EMA: EPAR PI
Finnish Swedish
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SPC
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Resepti
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Boostrix injektioneste, suspensio, esitäytetty ruisku PL 2024-05-30
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SPC
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Resepti
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Boostrix Polio injektioneste, suspensio, esitäytetty ruisku PL 2023-04-26
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European Medicines Agency's website: Bortezomib Accord - EMA: EPAR PI
Finnish Swedish
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European Medicines Agency's website: Bortezomib Accord - EMA: EPAR PI
Finnish Swedish
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SPC
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Resepti
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Bortezomib Avansor 2.5 mg, 3.5 mg injektiokuiva-aine, liuosta varten PL 2021-04-13
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SPC
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Resepti
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Bortezomib Baxter 3,5 mg injektiokuiva-aine, liuosta varten PL 2021-11-18
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SPC
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Resepti
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Bortezomib EVER Pharma 2.5 mg-ml injektioneste, liuos PL 2023-07-07
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European Medicines Agency's website: Bortezomib Fresenius Kabi - EMA: EPAR PI
Finnish Swedish
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European Medicines Agency's website: Bortezomib Hospira - EMA: EPAR PI
Finnish Swedish
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SPC
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Resepti
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Bortezomib Medac 3.5 mg injektiokuiva-aine, liuosta varten PL 2022-04-20
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SPC
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Resepti
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Bortezomib Medical Valley 3,5 mg injektiokuiva-aine, liuosta varten PL 2024-01-17
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SPC
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Resepti
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Bortezomib MSN 3.5 mg injektiokuiva-aine, liuosta varten PL 2022-06-21
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SPC
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Resepti
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Bortezomib Reddy 3,5 mg injektiokuiva-aine, liuosta varten PL 2022-09-05
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SPC
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Resepti
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Bortezomib STADA 2,5 mg-ml injektioneste, liuos PL 2022-08-16
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European Medicines Agency's website: Bortezomib Sun - EMA: EPAR PI
Finnish Swedish
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SPC
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Resepti
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Bortezomib Viatris 3,5 mg injektiokuiva-aine, liuosta varten PL 2023-06-20
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SPC
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Resepti
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Bosentan Accord 62.5 mg, 125 mg tabletti, kalvopäällysteinen PL 2022-09-06
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European Medicines Agency's website: Bosulif - EMA: EPAR PI
Finnish Swedish
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SPC
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Resepti
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Bosutinib Stada 100 mg, 400 mg, 500 mg tabletti, kalvopäällysteinen PL 2024-02-02
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SPC
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Resepti
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Botox 50, 100, 200 Allergan-yksikköä injektiokuiva-aine, liuosta varten PL 2024-06-10
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European Medicines Agency's website: Braftovi - EMA: EPAR PI
Finnish Swedish
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European Medicines Agency's website: Braftovi - EMA: EPAR PI
Finnish Swedish
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SPC
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Resepti
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Braltus 10 mikrog-vapautunut annos inhalaatiojauhe, kapseli, kova PL 2023-03-06
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European Medicines Agency's website: Bretaris Genuair - EMA: EPAR PI
Finnish Swedish
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SPC
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Resepti
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Brevibloc 10 mg-ml infuusioneste liuos PL 2015-07-09
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SPC
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Resepti
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Brevibloc 10 mg-ml infuusioneste, liuos PL 2024-08-31
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