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Summaries of Product Characteristics (SPC) for Human medicinal products
The summaries of product characteristics (SPC) contain the information relevant to the use of the medicinal products and of importance to health care professionals. The SPCs are published in Finnish; the use of Finnish key words in the search fields is therefore recommended.
Some of the medicinal products contain a condition relevant to the prescribing of the product and not always found in the SPC. The conditions for prescribing and the products covered by this condition are found in the FimeaWeb search.
The SPCs 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.
Summaries of Product Characteristics 91 - 120 of 257 |
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Package leaflet | Status for supply | Name of the medicinal product |
PL
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Resepti
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Bicain Spinal 5 mg-ml injektioneste, liuos SPC 2020-11-08
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PL
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Resepti
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Bicalutamid Orion 150 mg tabletti, kalvopäällysteinen SPC 2023-10-26
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PL
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Resepti
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Bicalutamid Orion 50 mg tabletti, kalvopäällysteinen SPC 2023-05-19
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PL
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Resepti
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Bicalutamide Accord 150 mg kalvopäällysteiset tabletit SPC 2022-11-09
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PL
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Resepti
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Bicavan 150 mg tabletti, kalvopäällysteinen SPC 2021-01-18
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PL
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Resepti
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Bicavan 50 mg tabletti, kalvopäällysteinen SPC 2021-01-18
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PL
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Resepti
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bicaVera 1.5 % glukoosi, 1,25 mmol-l kalsium, peritoneaalidialyysineste SPC 2023-06-21
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PL
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Resepti
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BicaVera 1.5 % glukoosi, 1,75 mmol-l kalsium, peritoneaalidialyysineste SPC 2023-09-29
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PL
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Resepti
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bicaVera 2.3 % glukoosi, 1,25 mmol-l kalsium, peritoneaalidialyysineste SPC 2023-06-21
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PL
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Resepti
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BicaVera 2.3 % glukoosi, 1,75 mmol-l kalsium, peritoneaalidialyysineste SPC 2023-09-29
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PL
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Resepti
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bicaVera 4.25 % glukoosi, 1,25 mmol-l kalsium, peritoneaalidialyysineste SPC 2023-06-21
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PL
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Resepti
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BicaVera 4.25 % glukoosi, 1,75 mmol-l kalsium, peritoneaalidialyysineste SPC 2023-09-29
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PL
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Resepti
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Bifril Comp 30 mg/12.5 mg tabletti SPC 2011-07-22
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European Medicines Agency's website: Biktarvy - EMA: EPAR PI
Finnish Swedish
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PL
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Resepti
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Bimatoprost Sandoz 0.3 mg-ml silmätipat, liuos SPC 2021-12-23
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PL
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Resepti
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Bimatoprost STADA 0,3 mg-ml silmätipat, liuos, kerta-annospakkaus SPC 2022-02-14
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PL
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Resepti
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Bimatoprost Stada 0.3 mg-ml silmätipat, liuos SPC 2022-01-03
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PL
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Resepti
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Bimatoprost-Timolol STADA 0,3 mg-ml + 5 mg-ml silmätipat, liuos, kerta-annospakkaus SPC 2024-01-22
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PL
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Resepti
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Bimatoprost-Timolol Stada 0.3 mg-ml + 5 mg-ml silmätipat, liuos SPC 2024-04-23
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European Medicines Agency's website: BIMERVAX - EMA: EPAR PI
Finnish Swedish
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European Medicines Agency's website: Bimzelx - EMA: EPAR PI
Finnish Swedish
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European Medicines Agency's website: Binocrit - EMA: EPAR PI
Finnish Swedish
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PL
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Resepti
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Binosto 70 mg poretabletti SPC 2021-06-29
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PL
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Resepti
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Bio-E-Vitamin 350 mg kapseli SPC 2015-06-18
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PL
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Resepti
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Bioclavid 500 mg - 125 mg tabletti, kalvopäällysteinen SPC 2023-02-10
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PL
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Resepti
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Bioclavid 80-11.4 mg-ml jauhe oraalisuspensiota varten SPC 2023-02-03
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PL
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Resepti
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Bioclavid 875 mg - 125 mg tabletti, kalvopäällysteinen SPC 2023-02-03
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European Medicines Agency's website: Biopoin - EMA: EPAR PI
Finnish Swedish
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PL
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Resepti
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Biphozyl hemodialyysi-hemofiltraationeste SPC 2021-09-01
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PL
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Resepti
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Biquetan 50 mg, 150 mg, 200 mg, 300 mg, 400 mg depottabletti SPC 2024-05-21
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