Drug Guide
Desogestrel; Ethinyl Estradiol
Classification
Therapeutic: Contraceptive, Hormonal
Pharmacological: Combination Estrogen-Progestin
FDA Approved Indications
- Prevention of pregnancy
Mechanism of Action
Inhibits ovulation through suppression of the hypothalamic-pituitary-ovarian axis, thickens cervical mucus, and alters the endometrial lining to prevent implantation.
Dosage and Administration
Adult: Typically, one tablet daily at the same time each day, starting on the first day of the menstrual cycle, with subsequent packs following sequentially.
Pediatric: Not indicated for use in children.
Geriatric: Not indicated for use in postmenopausal women.
Renal Impairment: Use with caution; no specific dosage adjustments established.
Hepatic Impairment: Contraindicated in women with significant liver disease.
Pharmacokinetics
Absorption: Rapidly absorbed from the gastrointestinal tract.
Distribution: Widely distributed; highly bound to plasma proteins.
Metabolism: Metabolized in the liver via hydroxylation and conjugation.
Excretion: Excreted mainly in urine and feces.
Half Life: Approximately 28 hours for Ethinyl Estradiol and 30-40 hours for Desogestrel.
Contraindications
- History of thromboembolic disorders
- Active or history of breast cancer
- Significant liver disease or tumors
Precautions
- Use with caution in women over 35 who smoke, women with hypertension, diabetes, or cardiovascular risk factors.
Adverse Reactions - Common
- Nausea (Common)
- Breast tenderness (Common)
- Irregular bleeding or spotting (Common)
Adverse Reactions - Serious
- Venous thromboembolism (Less common)
- Stroke or myocardial infarction (Rare)
- Liver tumors (Rare)
Drug-Drug Interactions
- Antibiotics (may reduce efficacy)
- Anticonvulsants (e.g., phenytoin, carbamazepine)
- Rifampin
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Assess blood pressure, thrombotic risk factors, and medication adherence.
Diagnoses:
- Risk for thromboembolism
- Deficient knowledge regarding contraceptive use
Implementation: Administer at the same time each day; counsel about adherence and contraindications.
Evaluation: Monitor for adverse effects, confirm effective contraception, and reassess risk factors periodically.
Patient/Family Teaching
- Take as directed at the same time daily.
- Use additional contraceptive methods if diarrheal or vomiting occurs.
- Report unusual symptoms like severe headache, visual changes, chest pain, or severe leg pain.
Special Considerations
Black Box Warnings:
- Smoking increases risk of cardiovascular events in women over 35 using combination hormonal contraceptives.
Genetic Factors: No specific genetic testing required.
Lab Test Interference: May affect results of thyroid and coagulation tests.
Overdose Management
Signs/Symptoms: Nausea, vomiting, vaginal bleeding.
Treatment: Supportive care, no specific antidote. In case of overdose, discontinue medication and observe.
Storage and Handling
Storage: Store at room temperature, 20-25°C (68-77°F).
Stability: Stable for the duration of the labeled shelf life when stored properly.