WHO Pharmaceuticals Newsletter 1999, No. 07&08
(1999; 18 pages)
Table of Contents
Close this folderRegulatory actions
View the documentAlbumin (human): review of safety: conclusions: UK
View the documentAstemizole: voluntary withdrawal: Janssen, USA
View the documentCisapride: revised labelling: QT syndrome and drug interactions: USA
View the documentFollitropin alfa: batch withdrawn: stability problems: EU
View the documentHetastarch (hydroxyethylstarch): fatal haemorrhages: France
View the documentMinocycline: immunoallergic and liver damage with long-term therapy: Germany
View the documentOral contraceptives containing gestodene or desogestrel: update: revised product information: UK
View the documentPemoline: revised labelling: liver function monitoring: Abbott, USA
View the documentPhenol: warning concerning topical solutions: New Zealand
View the documentProgestational drug products: requirements for patient labelling: proposed rule: USA
View the documentSubstandard medicines: distribution and prescription prohibited: Venezuela
View the documentSunscreen products: requirements: final rule: USA
View the documentTranylcypromine/trifluoperazine: licence not renewed: UK
View the documentTroglitazone: restricted indications: USA
View the documentTrovafloxacin and alatrofloxacin: suspended: Spain
Open this folder and view contentsDrug surveillance
Open this folder and view contentsNew developments
Open this folder and view contentsMedical devices
Open this folder and view contentsMedication errors
Open this folder and view contentsGeneral information
 

Oral contraceptives containing gestodene or desogestrel: update: revised product information: UK

United Kingdom. Further to safety concerns that have arisen in recent years about third- generation combined oral contraceptives containing desogestrel or gestodene, the Medicines Commission has further reviewed all currently available relevant data and has confirmed that the incidence of venous thromboembolism is about 25 per 100,000 women per year of use.

The incidence of venous thrombembolism in users of “second-generation” combined oral contraceptives (those containing levonorgestrel) is about 15 per 100,000 women per year of use. This indicates a small excess risk of about 10 cases of venous thromboembolism per 100,000 women years for women using third-generation combined oral contraceptives containing desogestrel or gestodene which has not been satisfactorily explained by bias or confounding. However, the absolute risk of venous thromboembolism in women taking combined oral contraceptives containing desogestrel or gestodene is very small and is much less than the risk of venous thromboembolism in pregnancy.

The Summaries of Product Characteristics (data sheets) and patient information leaflets for combined oral contraceptives containing desogestrel or gestodene will be updated to include the following statements:

Contraindications:

• History of confirmed venous thromboembolism (VTE). Family history of idiopathic VTE. Other known risk factors for VTE.

Warnings:

• An increased risk of venous thromboembolic disease (VTE) associated with the use of oral contraceptives is well established but is smaller than that associated with pregnancy, which has been estimated at 60 cases per 100,000 pregnancies. Some epidemiological studies have reported a greater risk of VTE for women using combined oral contraceptives containing desogestrel or gestodene (the so-called third generation pills) than for women using pills containing levonorgestrel (the so-called second generation pills). The spontaneous incidence of VTE in healthy non-pregnant women (not taking any oral contraceptive) is about 5 cases per 100,000 women per year. The incidence in users of second generation pills is about 15 per 100,000 women per year of use. The incidence in users of third generation pills is about 25 per 100,000 women per year of use: this excess incidence has not been satisfactorily explained by bias or confounding. The level of all of these risks of VTE increases with age and is likely to be increased in women with other known factors for VTE such as obesity.

Reference: Current Problems in Pharmacovigilance, Vol. 25, June 1999.

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Last updated: May 3, 2013