VISANNE Tablet Ref.[8727] Active ingredients: Dienogest

Source: European Medicines Agency (EU) 

Therapeutic indications

Treatment of endometriosis.

Posology and method of administration

Method of administration

For oral use.

Posology

The dosage of Visanne is one tablet daily without any break, taken preferably at the same time each day with some liquid as needed. The tablet can be taken with or without food.

Tablets must be taken continuously without regard to vaginal bleeding. When a pack is finished the next one should be started without interruption.

There is no experience with Visanne treatment >15 months in patients with endometriosis. Treatment can be started on any day of the menstrual cycle.

Any hormonal contraception needs to be stopped prior to initiation of Visanne. If contraception is required, non-hormonal methods of contraception should be used (e.g. barrier method).

Management of missed tablets

The efficacy of Visanne may be reduced in the event of missed tablets, vomiting and/or diarrhea (if occuring within 3-4 hours after tablet taking). In the event of one or more missed tablets, the woman should take one tablet only, as soon as she remembers, and should then continue the next day at her usual time. A tablet not absorbed due to vomiting or diarrhea should likewise be replaced by one tablet.

Additional information on special populations

Paediatric population

Visanne is not indicated in children prior to menarche.

The safety and efficacy of Visanne was investigated in an uncontrolled clinical trial over 12 months in 111 adolescent women (12-<18) with clinically suspected or confirmed endometriosis (see sections 4.4 and 5.1).

Geriatric population

There is no relevant indication for use of Visanne in the Geriatric population.

Patients with hepatic impairment

Visanne is contraindicated in patients with present or past severe hepatic disease (see section 4.3).

Patients with renal impairment

There are no data suggesting the need for a dosage adjustment in patients with renal impairment.

Overdose

Acute toxicity studies performed with dienogest did not indicate a risk of acute adverse effects in case of inadvertent intake of a multiple of the daily therapeutic dose. There is no specific antidote. A daily intake of 20-30 mg dienogest (10 to 15 times higher dose than in Visanne) over 24 weeks of use was very well tolerated.

Shelf life

5 years.

Special precautions for storage

Store in the original packaging to protect from light.

Nature and contents of container

The tablets are contained in blister packs consisting of green transparent films made of polyvinylidene chloride (PVDC) coated polyvinyl chloride (PVC) and metallic foils made of aluminum (mat side hot sealable).

Pack sizes: 28, 84 and 168 tablets.

Not all pack sizes may be marketed.

Special precautions for disposal and other handling

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

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