Metopirone®
metyrapone USP
Capsules
Diagnostic Test of Pituitary
Adrenocorticotropic Function
Prescribing Information
DESCRIPTION
Metopirone, metyrapone USP, is an inhibitor of endogenous adrenal corticosteroid synthesis, available
as 250-mg capsules for oral administration. Its chemical name is 2-methyl-1,
2-di-3-pyridyl-1-propanone, and its structural formula is
Metyrapone USP is a white to light amber, fine, crystalline powder, having a characteristic odor. It
is sparingly soluble in water, and soluble in methanol and in chloroform. It forms water-soluble salts
with acids. Its molecular weight is 226.28.
Inactive Ingredients. Polyethylene glycol, glycerine, gelatin, sodium ethyl hydroxybenzoate,
sodium propyl hydroxybenzoate, ethyl vanillin, 4-methoxyacetophenone, titanium dioxide, brown ink.
CLINICAL PHARMACOLOGY
Pharmacodynamics
The pharmacological effect of Metopirone is to reduce cortisol and corticosterone production by
inhibiting the 11-β-hydroxylation reaction in the adrenal cortex. Removal of the strong inhibitory
feedback mechanism exerted by cortisol results in an increase in adrenocorticotropic hormone (ACTH)
production by the pituitary. With continued blockade of the enzymatic steps leading to production of
cortisol and corticosterone, there is a marked increase in adrenocortical secretion of their immediate
precursors, 11-desoxycortisol and desoxycorticosterone, which are weak suppressors of ACTH release,
and a corresponding elevation of these steroids in the plasma and of their metabolites in the urine.
These metabolites are readily determined by measuring urinary 17-hydroxycorticosteroids (17-OHCS)
or 17-ketogenic steroids (17-KGS).
Reference ID: 2859992
Because of these actions, Metopirone is used as a diagnostic test, with urinary 17-OHCS measured as an
index of pituitary ACTH responsiveness. Metopirone may also suppress biosynthesis of aldosterone,
resulting in a mild natriuresis.
Pharmacokinetics
The response to Metopirone does not occur immediately. Following oral administration, peak steroid
excretion occurs during the subsequent 24-hour period.
Absorption
Metopirone is absorbed rapidly and well when administered orally as prescribed. Peak plasma
concentrations are usually reached 1 hour after administration. After administration of 750 mg, mean
peak plasma concentrations are 3.7 µg/mL, falling to 0.5 µg/mL 4 hours after administration. Following
a single 2000-mg dose, mean peak plasma concentrations of metyrapone in plasma are 7.3 µg/mL.
Metabolism
The major biotransformation is reduction of the ketone to metyrapol, an active alcohol metabolite.
Eight hours after a single oral dose, the ratio of metyrapone to metyrapol in the plasma is 1:1.5.
Metyrapone and metyrapol are both conjugated with glucuronide.
Excretion
Metyrapone is rapidly eliminated from the plasma. The mean ± SD terminal elimination half-life is 1.9
± 0.7 hours. Metyrapol takes about twice as long as metyrapone to be eliminated from the plasma.
After administration of 4.5 g metyrapone (750 mg every 4 hours), an average of 5.3% of the dose was
excreted in the urine in the form of metyrapone (9.2% free and 90.8% as glucuronide) and 38.5% in the
form of metyrapol (8.1% free and 91.9% as glucuronide) within 72 hours after the first dose was given.
INDICATIONS AND USAGE
Metopirone is a diagnostic drug for testing hypothalamic-pituitary ACTH function.
CONTRAINDICATIONS
Metopirone is contraindicated in patients with adrenal cortical insufficiency, or hypersensitivity to
Metopirone or to any of its excipients.
WARNINGS
Metopirone may induce acute adrenal insufficiency in patients with reduced adrenal secretory capacity.
PRECAUTIONS
General
Ability of adrenals to respond to exogenous ACTH should be demonstrated before Metopirone is
employed as a test. In the presence of hypo- or hyperthyroidism, response to the Metopirone test may
be subnormal.
Since Metopirone may cause dizziness and sedation, patients should exercise caution when driving
or operating machinery.
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Laboratory Tests
See INTERPRETATION.
Drug Interactions
Drugs affecting pituitary or adrenocortical function, including all corticosteroid therapy, must be
discontinued prior to and during testing with Metopirone.
The metabolism of Metopirone is accelerated by phenytoin; therefore, results of the test may be
inaccurate in patients taking phenytoin within two weeks before. A subnormal response may occur in
patients on estrogen therapy.
Metopirone inhibits the glucuronidation of acetaminophen and could possibly potentiate
acetaminophen toxicity.
Carcinogenesis, Mutagenesis, Impairment of Fertility
Long-term carcinogenicity and reproduction studies in animals have not been conducted.
Metopirone was not mutagenic with or without metabolic activation in three strains of bacteria.
Pregnancy Category C
A subnormal response to Metopirone may occur in pregnant women. Animal reproduction studies have
not been conducted with Metopirone. The Metopirone test was administered to 20 pregnant women in
their second and third trimester of pregnancy and evidence was found that the fetal pituitary responded
to the enzymatic block. It is not known if Metopirone can affect reproduction capacity. Metopirone
should be given to a pregnant woman only if needed.
Animal reproduction studies adequate to evaluate teratogenicity and postnatal development have
not been conducted with Metopirone.
Nursing Mothers
It is not known whether this drug is excreted in human milk. Because many drugs are excreted in
human milk, caution should be exercised when Metopirone is administered to a nursing woman.
Pediatric Use
See DOSAGE AND ADMINISTRATION.
Geriatric Use
Clinical studies of Metopirone did not include sufficient numbers of subjects aged 65 years and over to
determine whether they respond differently from younger subjects. Other reported clinical experience
has not identified differences in responses between the elderly and younger patients. In general, dose
selection for an elderly patient should be cautious, reflecting the greater frequency of decreased hepatic,
renal, or cardiac function, and of concomitant disease or other drug therapy.
ADVERSE REACTIONS
Cardiovascular System: Hypotension
Gastrointestinal System: Nausea, vomiting, abdominal discomfort or pain.
Central Nervous System: Headache, dizziness, sedation.
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Dermatologic System: Allergic rash.
Hematologic System: Rarely, decreased white blood cell count or bone marrow depression.
OVERDOSAGE
Acute Toxicity
One case has been recorded in which a 6-year-old girl died after two doses of Metopirone, 2 g.
Oral LD50 in animals (mg/kg): rats, 521; maximum tolerated intravenous dose in one dog, 300.
Signs and Symptoms
The clinical picture of poisoning with Metopirone is characterized by gastrointestinal symptoms and by
signs of acute adrenocortical insufficiency.
Cardiovascular System: Cardiac arrhythmias, hypotension, dehydration.
Nervous System and Muscles: Anxiety, confusion, weakness, impairment of consciousness.
Gastrointestinal System: Nausea, vomiting, epigastric pain, diarrhea.
Laboratory Findings: Hyponatremia, hypochloremia, hyperkalemia.
Combined Poisoning
In patients under treatment with insulin or oral antidiabetics, the signs and symptoms of acute poisoning
with Metopirone may be aggravated or modified.
Treatment
There is no specific antidote. Besides general measures to eliminate the drug and reduce its absorption,
a large dose of hydrocortisone should be administered at once, together with saline and glucose
infusions.
Surveillance: For a few days blood pressure and fluid and electrolyte balance should be monitored.
DOSAGE AND ADMINISTRATION
Single-Dose Short Test
This test, usually given on an outpatient basis, determines plasma 11-desoxycortisol and/or ACTH
levels after a single dose of Metopirone. The patient is given 30 mg/kg (maximum 3 g Metopirone) at
midnight with yogurt or milk. The same dose is recommended in children. The blood sample for the
assay is taken early the following morning (7:30-8:00 a.m.). The plasma should be frozen as soon as
possible. The patient is then given a prophylactic dose of 50 mg cortisone acetate.
Interpretation
Normal values will depend on the method used to determine ACTH and 11-desoxycortisol levels. An
intact ACTH reserve is generally indicated by an increase in plasma ACTH to at least 44 pmol/L (200
ng/L) or by an increase in 11-desoxycortisol to over 0.2 µmol/L (70 µg/L). Patients with suspected
adrenocortical insufficiency should be hospitalized overnight as a precautionary measure.
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Multiple-Dose Test
Day 1: Control period - Collect 24-hour urine for measurement of 17-OHCS or 17-KGS.
Day 2: ACTH test to determine the ability of adrenals to respond - Standard ACTH test such as
infusion of 50 units ACTH over 8 hours and measurement of 24-hour urinary steroids. If results
indicate adequate response, the Metopirone test may proceed.
Day 3-4: Rest period.
Day 5: Administration of Metopirone: Recommended with milk or snack.
Adults: 750 mg orally, every 4 hours for 6 doses. A single dose is approximately equivalent to 15
mg/kg.
Children: 15 mg/kg orally every 4 hours for 6 doses. A minimal single dose of 250 mg is
recommended.
Day 6: After administration of Metopirone - Determination of 24-hour urinary steroids for effect.
Interpretation
ACTH Test
The normal 24-hour urinary excretion of 17-OHCS ranges from 3 to 12 mg. Following continuous
intravenous infusion of 50 units ACTH over a period of 8 hours, 17-OHCS excretion increases to 15 to
45 mg per 24 hours.
Metopirone
Normal response: In patients with a normally functioning pituitary, administration of Metopirone is
followed by a two- to four-fold increase of 17-OHCS excretion or doubling of 17-KGS excretion.
Subnormal response: Subnormal response in patients without adrenal insufficiency is indicative of
some degree of impairment of pituitary function, either panhypopituitarism or partial hypopituitarism
(limited pituitary reserve).
1. Panhypopituitarism is readily diagnosed by the classical clinical and chemical evidences of
hypogonadism, hypothyroidism, and hypoadrenocorticism. These patients usually have subnormal basal
urinary steroid levels. Depending upon the duration of the disease and degree of adrenal atrophy, they
may fail to respond to exogenous ACTH in the normal manner. Administration of Metopirone is not
essential in the diagnosis, but if given, it will not induce an appreciable increase in urinary steroids.
2. Partial hypopituitarism or limited pituitary reserve is the more difficult diagnosis as these patients do
not present the classical signs and symptoms of hypopituitarism.
Reference ID: 2859992
Measurements of target organ functions often are normal under basal conditions. The response to
exogenous ACTH is usually normal, producing the expected rise of urinary steroids (17-OHCS or 17
KGS).
The response, however, to Metopirone is subnormal; that is, no significant increase in 17-OHCS or
17-KGS excretion occurs.
This failure to respond to metyrapone may be interpreted as evidence of impaired pituitary-adrenal
reserve. In view of the normal response to exogenous ACTH, the failure to respond to metyrapone is
inferred to be related to a defect in the CNS-pituitary mechanisms which normally regulate ACTH
secretions. Presumably the ACTH secreting mechanisms of these individuals are already working at
their maximal rates to meet everyday conditions and possess limited “reserve” capacities to secrete
additional ACTH either in response to stress or to decreased cortisol levels occurring as a result of
metyrapone administration.
Subnormal response in patients with Cushing’s syndrome is suggestive of either autonomous
adrenal tumors that suppress the ACTH-releasing capacity of the pituitary or nonendocrine ACTH-
secreting tumors.
Excessive response: An excessive excretion of 17-OHCS or 17-KGS after administration of
Metopirone is suggestive of Cushing’s syndrome associated with adrenal hyperplasia. These patients
have an elevated excretion of urinary corticosteroids under basal conditions and will often, but not
invariably, show a “supernormal” response to ACTH and also to Metopirone, excreting more than 35
mg per 24 hours of either 17-OHCS or 17-KGS.
HOW SUPPLIED
Capsules 250 mg -- soft gelatin, white to yellowish-white, oblong, opaque, imprinted CIBA on one side
and LN on the other side in brown ink.
Bottles of 18………………………………………………………………NDC 0078-0455-17
Do not store above 30ºC (86ºF).
Protect from moisture and heat.
Dispense in tight container (USP).
T20
REV:
Manufactured by:
R.P. Scherer GmbH
Eberbach/Baden, Germany
Distributed by:
Novartis Pharmaceuticals Corporation
East Hanover, New Jersey 07936
© Novartis
Reference ID: 2859992
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