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Pronunciation |
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(yoor
oh fol li TROE
pin) |
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U.S. Brand
Names |
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Fertinex® Injection; Metrodin®
Injection |
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Generic
Available |
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No |
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Pharmacological Index |
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Ovulation Stimulator |
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Use |
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Induction of ovulation in patients with polycystic ovarian disease and to
stimulate the development of multiple oocytes |
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Pregnancy Risk
Factor |
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X |
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Contraindications |
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Hypersensitivity to urofollitropin; high levels of both LH and FSH indicating
primary ovarian failure; uncontrolled thyroid or adrenal dysfunction; organic
intracranial lesion such as a pituitary tumor; presence of any cause of
infertility other than anovulation, unless the patient is a candidate for in
vitro fertilization; abnormal bleeding of undetermined nature; ovarian cysts
or enlargement not due to polycystic ovarian disease; pregnancy (may cause fetal
harm) |
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Warnings/Precautions |
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Use lowest dose possible to avoid abnormal ovarian enlargement. If
hyperstimulation occurs, discontinue use and hospitalize patient. Use with
caution in patients with a history of thromboembolism. |
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Adverse
Reactions |
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>10%:
Endocrine & metabolic: Ovarian enlargement or ovarian cysts
Local: Edema at injection site, pain at injection site
1% to 10%:
Cardiovascular: Arterial thromboembolism
Central nervous system: Fever, chills
Dermatologic: Rash or hives
Endocrine & metabolic: Breast tenderness
Gastrointestinal: Nausea, vomiting, abdominal pain, diarrhea
Miscellaneous: Hyperstimulation syndrome |
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Overdosage/Toxicology |
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Symptoms of overdose include possible hyperstimulation and multiple
gestations. Supportive care to maintain fluid and electrolyte imbalance may be
needed. |
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Drug
Interactions |
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No data reported |
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Mechanism of
Action |
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Preparation of follicle-stimulating hormone 75 IU with <1 IU of
luteinizing hormone (LH) which is isolated from the urine of postmenopausal
women. Follicle-stimulating hormone plays a role in the development of
follicles. Elevated FSH levels early in the normal menstrual cycle are thought
to play a significant role in recruiting a cohort of follicles for maturation. A
single follicle is enriched with FSH receptors and becomes dominant over the
rest of the recruited follicles. The increased number of FSH receptors allows it
to grow despite declining FSH levels. This dominant follicle secretes low levels
of estrogen and inhibin which further reduces pituitary FSH output. The ovarian
stroma, under the influence of luteinizing hormone, produces androgens which the
dominant follicle uses as precursors for estrogens. |
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Pharmacodynamics/Kinetics |
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Serum half-life, elimination: 3.9 hours and 70.4 hours (FSH has two
half-lives) |
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Usual Dosage |
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Adults: Female: S.C.: 75 units/day for 7-12 days, used with hCG may repeat
course of treatment 2 more times |
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Administration |
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Give via micron filter needle |
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Dental Health: Local
Anesthetic/Vasoconstrictor
Precautions |
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No information available to require special precautions |
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Dental Health:
Effects on Dental Treatment |
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No effects or complications reported |
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Patient
Information |
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This drug must be given according to a set schedule. Maintain a calendar of
treatment days and ovulation days. Engage in intercourse daily beginning on the
day prior to hCG administration until ovulation is apparent. Be aware that
multiple births may result. You may experience flushing, abdominal distention,
or breast tenderness. Report pain or heat in calves, fever, chills, rash, or
difficulty breathing. Pregnancy/breast-feeding precautions: Inform
prescriber if pregnant. Do not breast-feed. |
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Nursing
Implications |
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Stability: Protect from light; refrigerate at 3°C to
25°C (37°F to
77°F) |
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Dosage Forms |
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Injection: 0.83 mg [75 units FSH activity] (2 mL); 1.66 mg [150 units FSH
activity] |
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