Verzenios ® (abemaciklib)

För fullständig produktresumé för Verzenios se FASS.

Denna information är endast avsedd för sjukvårdspersonal verksam i Sverige och som svar på din fråga. Informationen nedan är på engelska

Verzenios® ▼ (abemaciclib): Förvaring och förpackning

Verzenios (abemaciclib) kräver inga speciella förvaringsanvisningar.

Dosage Form

PCTFE/PE/PVC blisters sealed with an aluminium foil in a calendar blister card, in packs of 14, 28, 42, 56, 70 or 168 film-coated tablets.1

Aluminium/aluminium perforated unit dose blisters of 28 x 1 film-coated tablets.1

Not all pack sizes may be marketed.1

Table 1.  Abemaciclib qualitative and quantitative composition1

Verzenios 50 mg film-coated tablets

Beige, oval tablet of 5.2 x 9.5 mm, debossed with “Lilly” on one side and “50” on the other.

Verzenios 100 mg film-coated tablets

White, oval tablet of 6.6 x 12.0 mm, debossed with “Lilly” on one side and “100” on the other.

Verzenios 150 mg film-coated tablets

Yellow, oval tablet of 7.5 x 13.7 mm, debossed with “Lilly” on one side and “150” on the other.


Abemaciclib  is for oral use.1

Patients should take the doses at approximately the same times every day.

The tablet should be swallowed whole (patients should not chew, crush, or split tablets before swallowing).1

If a patient vomits or misses a dose of abemaciclib, the patient should be instructed to take the next dose at its scheduled time; an additional dose should not be taken.1


This medicinal product does not require any special storage conditions.1


Any unused medicinal product or waste material should be disposed of in accordance with local requirements.1


1. Verzenios [summary of product characteristics]. Eli Lilly Nederland B.V., The Netherlands.


MSDS =  Material Safety Data Sheet

PCTFE = Polychlorotrifluoroethylene

PE = Polyethylene

PVC = Polyvinyl Chloride

This medicinal product is subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse reactions.

Datum fӧr senaste ӧversyn 2019 M01 03

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