What kind of pill is azurette

Steroid hormones may be poorly metabolized in patients with liver impairment. Acute or chronic disturbances of liver function may necessitate the discontinuation of COC use until markers of liver function return to normal and COC causation has been excluded.

Hepatic adenomas are associated with COC use. An estimate of the attributable risk is 3. Rupture of hepatic adenomas may cause death through intra-abdominal hemorrhage. Studies have shown an increased risk of developing hepatocellular carcinoma in long term more than 8 years COC users. However, the attributable risk of liver cancers in COC users is less than 1 case per million users.

Use COCs with caution in patients with pre-existing gallbladder disease; however, recent studies have shown that the relative risk of developing gallbladder disease among COC users appears minimal due to the use of products that contain lower doses of hormones. Mood disorders, like depression, may be aggravated in women taking hormones or combined oral hormonal contraceptives COCs.

Data regarding the association of COCs with onset of depression or exacerbation of existing depression are limited. If significant depression occurs, desogestrel; ethinyl estradiol should be discontinued. Desogestrel; ethinyl estradiol is contraindicated in patients with a history of, or known or suspected breast cancer, as breast cancer is a hormonally-sensitive tumor. All women taking combined oral contraceptives COCs should receive clinical breast examinations and perform monthly self-examinations as recommended by their health care professional based on patient age, known risk factors, and current standards of care.

There is substantial evidence that use of COCs does not increase the incidence of breast cancer. Although some past studies have suggested that COCs might increase the incidence of breast cancer, more recent studies have not confirmed such findings. Several large, well-designed observational studies have provided data regarding the risk of breast cancer with combined oral contraceptive COC use.

From one large study published in , the risk of breast cancer was higher among women who currently or recently used contemporary hormonal contraceptives than among women who had never used hormonal contraceptives, and this risk increased with longer durations of use; however, absolute increases in risk were small.

The absolute risk of breast cancer associated with any hormonal contraceptive use was 13 per , women-years, which corresponds to 1 extra case of breast cancer for every 7, COC users in 1 year. Moreover, the same study data suggest that any increased risk of breast cancer usually disappears rapidly after an interruption in the use of COCs.

There continues to be controversy regarding the risk of COC use in women with a family history of breast cancer e. However, evidence does not suggest that the increased risk for breast cancer among women with either a family history of breast cancer or breast cancer susceptibility genes is modified by the use of COCs.

Patients should be instructed to perform monthly self-breast examination and report any breast changes, lumps, or discharge to their health care professional. If breast cancer is suspected in a woman who is taking hormonal contraceptives, the contraceptive should be discontinued. Desogestrel; ethinyl estradiol is contraindicated in the presence of cervical cancer or other estrogen-responsive tumors. Most cervical cancers are related to the presence of the human papillomavirus HPV , but hormonal factors influence risk.

In women taking COCs, studies have found a slightly increased risk of cervical cancer compared with never-users. The risk appears to increase with duration of use and appears to decline when COCs are discontinued. Clinical surveillance of all women using COCs is important; all women receiving COC treatment should have a pelvic examination and other diagnostic or screening tests, such as cervical cytology, as clinically indicated or as generally recommended based on age, risk factors, and other individual needs.

In those women with known endometrial cancer or other estrogen-dependent tumors e. Hormonal contraceptives are contraindicated in women with undiagnosed vaginal bleeding; evaluate such patients before combined hormonal contraceptive use to determine if a contraindication to use exists. The use of combined oral contraceptives COCs appears to have a protective effect against some cancers. In women using COCs, a meta-analysis of 10 studies indicates a significant trend in decreasing endometrial and ovarian cancer risk with increasing duration of COC use.

The estrogen component of combined oral hormonal contraceptives may raise the serum concentrations of thyroid-binding globulin, sex hormone-binding globulin, and cortisol-binding globulin. Doses of thyroid hormone replacement for hypothyroidism may need to be increased, as indicated by clinical and laboratory monitoring for the individual. Cortisol replacement therapy e. Chloasma may occur with combined oral hormonal contraceptive COC use, especially in women with a history of chloasma gravidarum melasma.

Advise females who tend to develop chloasma to avoid exposure to the sun or ultraviolet UV exposure while taking desogestrel; ethinyl estradiol. Preexisting morbid obesity is one factor that may increase cardiovascular or thromboembolic risks associated with combination hormonal contraceptive use. Consider the presence of obesity and other underlying risk factors that may increase the risk of cardiovascular disease or thromboembolism, particularly for women over 35 years of age.

Limited literature suggests that the effectiveness of some hormonal contraceptive formulations might decrease with increasing body mass index BMI. However, the evidence is conflicting; there are also data to suggest that the efficacy of most combined hormonal contraceptive products with a few known exceptions does not seem to be compromised in women who are overweight.

The safety and efficacy of hormonal contraceptive products, like desogestrel; ethinyl estradiol, have only been established in females of reproductive age. Safety and efficacy of hormonal birth control is expected to be the same for postpubertal children under the age of 16 and for users 16 years of age and older. Use of hormonal contraceptive products in female children before menarche is not indicated. PDR Search. Required field. Your Name Your name is required.

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Jump to Section. BOXED WARNING Atrial fibrillation, cardiac disease, cerebrovascular disease, coronary artery disease, coronary thrombosis, edema, endocarditis, hypercholesterolemia, hypertension, myocardial infarction, protein C deficiency, protein S deficiency, renal disease, stroke, thromboembolic disease, thromboembolism, thrombophlebitis, tobacco smoking, valvular heart disease. Oral dosage monophasic products containing 0. Adult and Adolescent females.

Oral dosage biphasic regimens, e. Oral dosage Triphasic regimen, e. Oral dosage all formulations. One, they stop you from ovulating releasing an egg from your ovary. Two, they cause changes in your cervix and uterus that make it harder for you to get pregnant.

Azurette and Kariva do not protect you against infection with HIV or other sexually transmitted diseases. Azurette and Kariva are tablets that you take by mouth. They come in blister packs with 28 tablets per pack. In each pack, 26 tablets contain hormones, and the other two do not.

For each cycle, you would take:. Insurance companies are more likely to cover generics than brand-name drugs because generics are cheaper. That means Azurette and Kariva are more likely to be covered than the brand-name version, Mircette.

Also, the cash price what you would pay without insurance for generic drugs may be less than for brand-name drugs. With or without insurance, both Azurette and Kariva would likely be cheaper than Mircette. All drugs can cause side effects. Some effects are more common and may go away after a few days. Others are more serious. These side effects can require medical care. Azurette, Kariva, and all other birth control pills have similar common side effects.

These include:. Azurette and Kariva have similar serious side effects. These side effects are rare in healthy women. They include:. An interaction is when a substance changes the way a drug works. An interaction can harm you or prevent the drug from working well.

Certain drugs may interact with Azurette and Kariva and other birth control pills. Examples of drugs that may interact with Azurette or Kariva include:. These drugs may make your birth control pills less effective in preventing pregnancy.

Why Nurx? Product details Take control of your reproductive health with Azurette, a combination hormone birth control pill that helps regulate your menstrual cycle. Download WordPress Themes Free. Download Nulled WordPress Themes. Tags Less painful periods Decreases risk of ovarian cysts Helps prevent pregnancy Can make periods more regular Helps treat acne Decreased blood flow during periods. Active Ingredients White tablets: desogestrel [0. Risks Using this medication does not protect you against sexually transmitted infections STIs Increased risk of blood clots Can cause allergic reaction Must be taken at the same time each day.

If you have an upset stomach, take Azurette after your evening meal. We are doctors, nurses, nurse practitioners, pharmacists, and physician assistants who are passionate about providing patient care.

The Nurx medical team believes that everyone deserves access to personalized, non-judgmental healthcare, and that open and honest communication is key. How It Works. Select your medication, or get guidance from our medical team. Answer a few questions and enter your insurance info if you have coverage - if not, no problem. A Nurx provider in your state will review your request and write a prescription, if appropriate.

We deliver your medication directly to you. On time, in a discreet package, and with no added costs. As Seen On. Premium WordPress Themes Download. Download WordPress Themes.