etonogestrel implant (Implanon)
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Introduction
single-rod, progestin-only, subdermal contraceptive
Indications
- prevention of pregnancy for up to 3 years
Contraindications
- pregnancy
- history of thromboembolism
- acute hepatic disease or tumor
- breast cancer or high risk patient
Dosage
- Each rod contains 68 mg of etonogestrel, which releases etonogestrel
- 60-70 ug/day for 5-6 weeks
- 35-45 ug/day at 1 year
- 30-40 ug/day at 2 years
- 25-35 ug/day at the end of 3 years
Must be removed at the end of 3 year period; may be replaced by a new Implanon rod
Rod is 4 cm x 2 cm, preloaded disposable applicator
Implanted subdermally into the inner side of the non-dominant arm 6-8 cm above the elbow crease overlying the groove between the biceps & triceps.
Implant between days 1 & 5 of the menstrual cycle, within 7 days of the last oral contraceptive, or within 5 days of 1st trimester miscarriage or abortion.
Pharmacokinetics
Adverse effects
- spotting, menorrhagia or other vaginal bleeding irregularities (11-18%)
- amenorrhea (22%)
- headache (25%)
- vaginitis (14%)
- weight gain 14%
- acne (14%)
- mastodynia (13%)
- upper respiratory tract infection (13%)
- abdominal pain (11%)
- pharyngitis (10%)
Drug interactions
- potent inducers of cyt P450 3A4 may diminish effectiveness of implanon
- inhibitors of cyt P450 3A4 may increase concentrations of etonogestrel
Notes
cost (2006) $523
More general terms
Components
References
- ↑ Prescriber's Letter 13(9): 2006 Etonogestrel Implant (Implanon) Detail-Document#: http://prescribersletter.com/(5bhgn1a4ni4cyp2tvybwfh55)/pl/ArticleDD.aspx?li=1&st=1&cs=&s=PRL&pt=3&fpt=25&dd=220922&pb=PRL (subscription needed) http://www.prescribersletter.com