Information
About Mircette
IMPORTANT NOTE:
The following information is intended to supplement,
not substitute for, the expertise and judgment of your
physician, pharmacist or other healthcare professional.
It should not be construed to indicate that use of the
drug is safe, appropriate, or effective for you. Consult
your healthcare professional before using this drug.
How To Use
To achieve maximum contraceptive effectiveness, Mircette
(desogestrel/ethinyl estradiol and ethinyl estradiol)
Tablets must be taken exactly as directed and at intervals
not exceeding 24 hours. Mircette may be initiated
using either a Sunday start or a Day 1 start. If you
do not understand these directions, ask your pharmacist,
nurse, or doctor to explain them to you.
Precautions
Oral contraceptives should not be used in women who
currently have the following conditions: thrombophlebitis
or thromboembolic disorders, past history of deep
vein thrombophlebitis or thromboembolic disorders,
cerebral vascular or coronary artery disease, known
or suspected carcinoma of the breast, carcinoma of
the endometrium or other known or suspected estrogen-dependent
neoplasia, undiagnosed abnormal genital bleeding,
cholestatic jaundice of pregnancy or jaundice with
prior pill use, hepatic adenomas of carcinomas, known
or suspected pregnancy. Oral contraceptives may compound
the effects of well-known risk factors, such as hypertension,
diabetes, hyperlipidemias ,and obesity. In particular,
some progestogens are known to decrease HDL cholesterol
and cause glucose intolerance, while estrogens may
create a state of hyperinsulinism. Oral contraceptives
have been shown to increase blood pressure among users.
Similar effects on risk factors have been associated
with an increased risk of heart disease. Oral contraceptives
must be used with caution in women with cardiovascular
disease risk factors.
Side Effects
An increased risk of the following serious adverse
reactions has been associated with the use of oral
contraceptives: thrombophlebitis and venous thrombosis,
arterial thromboembolism, pulmonary embolism, myocardial
infarction, cerebral hemorrhage, cerebral thrombosis,
hypertension, gallbladder disease, and hepatic adenomas
or benign liver tumors. The following adverse reactions
have been reported in patients receiving oral contraceptives
and are believed to be drug-related: nausea, vomiting,
gastrointestinal symptoms (such as abdominal cramps
and bloating), change in menstrual flow, amenorrhea,
temporary infertility after discontinuation of treatment,
Edema Melasma which may persist, breast changes: tenderness,
enlargement, secretion, Change in weight (increase
or decrease), change in cervical erosion and secretion,
diminution in lactation when given immediately postpartum,
cholestatic jaundice, Migraine Rash (allergic), mental
depression, reduced tolerance to carbohydrates, vaginal
candidiasis, change in corneal curvature (steepening),
intolerance to contact lenses, etc. The following
adverse reactions have been reported in users of oral
contraceptives and the association has been neither
confirmed nor refuted: pre-menstrual syndrome, cataracts,
changes in appetite, cystitis-like syndrome, headache,
nervousness, dizziness, hirsutism, loss of scalp hair,
erythema multiforme, erythema nodosum, hemorrhagic
eruption, vaginitis, porphyria, impaired renal function,
hemolytic uremic syndrome, acne, changes in libido,
colitis, Budd-Chiari Syndrome, effects on menses (increased
menstrual cycle regularity, decreased blood loss and
decreased incidence of iron deficiency anemia, decreased
incidence of dysmenorrhea), effects related to inhibition
of ovulation (decreased incidence of functional ovarian
cysts, decreased incidence of ectopic pregnancies).
Storage
Store Mircette at room temperature away from moisture
and heat.
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