Propylthiouracil: Difference between revisions

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|adverseReactions=[[nausea]], [[vomiting]], [[epigastric distress]], [[loss of taste]], [[arthralgia]], [[paresthesias]], [[myalgia]], [[headache]], [[drowsiness]], [[pruritus]], [[skin rash]] and [[urticaria]]
|adverseReactions=[[nausea]], [[vomiting]], [[epigastric distress]], [[loss of taste]], [[arthralgia]], [[paresthesias]], [[myalgia]], [[headache]], [[drowsiness]], [[pruritus]], [[skin rash]] and [[urticaria]]
|blackBoxWarningTitle=WARNING
|blackBoxWarningTitle=WARNING
|blackBoxWarningBody=* Severe liver injury and acute [[liver failure]], in some cases fatal, have been reported in patients treated with propylthiouracil. These reports of hepatic reactions include cases requiring liver transplantation in adult and pediatric patients.
|blackBoxWarningBody=* Severe liver injury and acute liver failure, in some cases fatal, have been reported in patients treated with propylthiouracil. These reports of hepatic reactions include cases requiring liver transplantation in adult and pediatric patients.


* Propylthiouracil should be reserved for patients who can not tolerate methimazole and in whom radioactive iodine therapy or surgery are not appropriate treatments for the management of [[hyperthyroidism]].
* Propylthiouracil should be reserved for patients who can not tolerate methimazole and in whom radioactive iodine therapy or surgery are not appropriate treatments for the management of hyperthyroidism.


* Because of the risk of fetal abnormalities associated with methimazole, proplythiouracil may be the treatment of choice when an antithyroid drug is indicated during or just prior to the first trimester of pregnancy.
* Because of the risk of fetal abnormalities associated with methimazole, proplythiouracil may be the treatment of choice when an antithyroid drug is indicated during or just prior to the first trimester of pregnancy.
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<!--Contraindications-->
<!--Contraindications-->
|contraindications=* Propylthiouracil is [[contraindicated]] in patients who have demonstrated [[hypersensitivity]] to the drug or any of the other product components.
|contraindications=* Propylthiouracil is [[contraindicated]] in patients who have demonstrated [[hypersensitivity]] to the drug or any of the other product components.
|warnings=====Liver Toxicity=====
|warnings=====Liver Toxicity====


* [[Hepato-biliary diseases|Liver injury]] resulting in [[liver failure]], [[liver transplantation]], or [[death]], has been reported with propylthiouracil therapy in adult and [[pediatric]] patients. No cases of [[liver failure]] have been reported with the use of [[methimazole]] in [[pediatric]] patients. For this reason, propylthiouracil is not recommended for [[pediatric]] patients except when [[methimazole]] is not well-tolerated and [[surgery]] or [[radioactive iodine]] therapy are not appropriate therapies.
* [[Hepato-biliary diseases|Liver injury]] resulting in [[liver failure]], [[liver transplantation]], or [[death]], has been reported with propylthiouracil therapy in adult and [[pediatric]] patients. No cases of [[liver failure]] have been reported with the use of [[methimazole]] in [[pediatric]] patients. For this reason, propylthiouracil is not recommended for [[pediatric]] patients except when [[methimazole]] is not well-tolerated and [[surgery]] or [[radioactive iodine]] therapy are not appropriate therapies.
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=====General=====
=====General=====


* Patients should be instructed to report any symptoms of hepatic dysfunction (anorexia, pruritus, jau7ndice, light colored stools, dark urine, right upper quadrant pain, etc.), particularly in the first six months of therapy. When these symptoms occur, measurement should be made of liver function (bilirubin, alkaline phosphatase) and hepatocellular integrity (ALT/AST levels).
* Patients should be instructed to report any symptoms of [[hepatic dysfunction]] ([[anorexia]], [[pruritus]], [[jaundice]], [[jaundice|light colored stools]], [[jaundice|dark urine]], [[right upper quadrant pain]], etc.), particularly in the first six months of therapy. When these symptoms occur, measurement should be made of [[liver function]] ([[bilirubin]], [[alkaline phosphatase]]) and [[Liver|hepatocellular integrity]] ([[ALT]]/[[AST]] levels).


* Patients who receive propylthiouracil should be under close surveillance and should be counseled regarding the necessity of reporting any evidence of illness, particularly sore throat, skin eruptions, fever, headache, or general malaise. In such cases, white blood cell and differential counts should be obtained to determine whether agranulocytosis has developed. Particular care should be exercised with patients who are receiving concomitant drugs known to be associated with agranulocytosis.
* Patients who receive propylthiouracil should be under close surveillance and should be counseled regarding the necessity of reporting any evidence of [[illness]], particularly [[sore throat]], [[skin changes|skin eruptions]], [[fever]], [[headache]], or [[malaise|general malaise]]. In such cases, [[White blood cells|white blood cell and differential counts]] should be obtained to determine whether [[agranulocytosis]] has developed. Particular care should be exercised with patients who are receiving concomitant drugs known to be associated with [[agranulocytosis]].
|clinicalTrials=* Major adverse reactions (much less common than the minor adverse reactions) include liver injury resulting in hepatitis, [[liver failure]], a need for liver transplantation or death. Inhibition of myelopoiesis (agranulocytosis, granulopenia, and thrombocytopenia), aplastic anemia, drug fever, a lupus-like syndrome (including splenomegaly and vasculitis), hepatitis, periartentis, and hypoprothrombinemia and bleeding have been reported. Nephritis, glomerulonephritis, interstitial pneumonitis, exfoliative dermatitis, and erythema nodosum have been reported. Reports of a vasculitis syndrome associated with the presence of anti-neutrophilic cytoplasmic antibodies (ANCA) have also been received. Manifestations of ANCA-positive vasculitis may include rapidly progressive glomerulonephritis (crescentic and pauci-immune necrotizing glomerulonephritis), sometimes leading to acute renal failure; pulmonary infiltrates or alveolar hemorrhage; skin ulcers; and leucocytoclastic vasculitis. Minor adverse reactions include skin rash, urticaria, nausea, vomiting, epigastric distress, arthralgia, paresthesias, loss of taste, taste perversion, abnormal Ioss of hair, myalgia, headache, pruritus, drowsiness, neuritis, edema, vertigo, skin pigmentation, jaundice, sialadenopathy, and lymphadenopathy.
|clinicalTrials=* Major adverse reactions (much less common than the minor adverse reactions) include [[hepatitis|liver injury]] resulting in [[hepatitis]], [[liver failure]], a need for [[liver transplantation]] or [[death]]. [[WBC|Inhibition of myelopoiesis]] ([[agranulocytosis]], [[granulopenia]], and [[thrombocytopenia]]), [[aplastic anemia]], [[drug fever]], a [[Lupus|lupus-like syndrome]] (including [[splenomegaly]] and [[vasculitis]]), [[hepatitis]], [[Arteritis|periartentis]], and [[hypoprothrombinemia]] and [[bleeding]] have been reported. [[Nephritis]], [[glomerulonephritis]], [[interstitial pneumonitis]], [[exfoliative dermatitis]], and [[erythema nodosum]] have been reported. Reports of a [[vasculitis]] syndrome associated with the presence of [[ANCA|Arteritisanti-neutrophilic cytoplasmic antibodies]] ([[ANCA]]) have also been received. Manifestations of [[vasculitis|ANCA-positive vasculitis]] may include [[rapidly progressive glomerulonephritis]] ([[Glomerulonephritis|crescentic and pauci-immune necrotizing glomerulonephritis]]), sometimes leading to [[acute renal failure]]; [[Pulmonary disease|pulmonary infiltrates]] or [[alveolar|alveolar hemorrhage]]; [[ulcers|skin ulcers]]; and [[vasculitis|leucocytoclastic vasculitis]]. Minor [[adverse reactions]] include [[skin rash]], [[urticaria]], [[nausea]], [[vomiting]], [[epigastric distress]], [[arthralgia]], [[paresthesias]], [[loss of taste]], [[taste perversion]], [[hair loss|abnormal Ioss of hair]], [[myalgia]], [[headache]], [[pruritus]], [[drowsiness]], [[neuritis]], [[edema]], [[vertigo]], [[skin pigmentation]], [[jaundice]], [[sialadenopathy]], and [[lymphadenopathy]].


* It should be noted that about 10% of patients with untreated [[hyperthyroidism]] have leukopenia (white blood cell count of less than 4,000/mm3), often with relative granulopenia.
* It should be noted that about 10% of patients with untreated [[hyperthyroidism]] have [[leukopenia]] ([[white blood cell count]] of less than 4,000/mm3), often with relative [[granulopenia]].


* To report SUSPECTED ADVERSE REACTIONS, contact West-ward Pharmaceutical Corp. at 1-877-233-2001 or the FDA at 1-800-FDA-1088 or WWW.FDA.GOV/MEDWATCH.
* To report SUSPECTED ADVERSE REACTIONS, contact West-ward Pharmaceutical Corp. at 1-877-233-2001 or the FDA at 1-800-FDA-1088 or WWW.FDA.GOV/MEDWATCH.
|postmarketing=There is limited information regarding <i>Postmarketing Experience</i> of {{PAGENAME}} in the drug label.
|postmarketing=There is limited information regarding <i>Postmarketing Experience</i> of {{PAGENAME}} in the drug label.
|drugInteractions======Anticoagulants (oral)=====
|drugInteractions=====Anticoagulants (oral)=====


* Due to the potential inhibition of vitamin K activity by propylthiouracil, the activity of oral anticoagulants (e.g., warfarin) may be increased; additional monitoring of PT/INR should be considered, especially before surgical procedures.
* Due to the potential inhibition of [[vitamin K]] activity by propylthiouracil, the activity of [[anticoagulants|oral anticoagulants]] (e.g., [[warfarin]]) may be increased; additional monitoring of [[PT]]/[[INR]] should be considered, especially before [[surgical procedures]].


=====Beta-adrenergic blocking agents=====
=====Beta-adrenergic blocking agents=====


* [[hyperthyroidism]] may cause an increased clearance of beta blockers with a high extraction ratio. A reduced dose of beta-adrenergic blockers may be needed when a hyperthyroid patient becomes euthyroid.
* [[Hyperthyroidism]] may cause an increased clearance of [[beta blockers]] with a high extraction ratio. A reduced dose of [[beta-adrenergic blockers]] may be needed when a [[hyperthyroid]] patient becomes [[euthyroid]].


=====Digitalis Glycosides=====
=====Digitalis Glycosides=====


* Serum digitalis levels may be increased when hyperthyroid patients on a stable digitalis glycoside regimen become euthyroid; a reduced dosage of digitalis glycosides may be needed.
* Serum [[digitalis]] levels may be increased when [[hyperthyroid]] patients on a stable [[digitalis glycoside]] regimen become [[euthyroid]]; a reduced dosage of [[digitalis glycosides]] may be needed.


=====Theophylline=====
=====Theophylline=====


* Theophylline clearance may decrease when hyperthyroid patients on a stable theophylline regimen become euthyroid; a reduced dose of theophylline may be needed.
* [[Theophylline|Theophylline clearance]] may decrease when [[hyperthyroid]] patients on a stable [[theophylline]] regimen become [[euthyroid]]; a reduced dose of [[theophylline]] may be needed.
|FDAPregCat=D
|FDAPregCat=D
|useInPregnancyFDA=* There are cases of liver injury, including liver faillure and death, in women treated with propylthiouracil during pregnancy. Two reports of in utero exposure with [[liver failure]] and death of a newborn have been reported. The use of an alternative antithyroid medication (e.g., methimazole) may be advisable following the first trimester of pregnancy.
|useInPregnancyFDA=* There are cases of liver injury, including [[Hepatic failure|liver faillure]] and [[death]], in women treated with propylthiouracil during [[pregnancy]]. Two reports of in utero exposure with [[liver failure]] and death of a newborn have been reported. The use of an alternative [[antithyroid medication]] (e.g., [[methimazole]]) may be advisable following the [[first trimester of pregnancy]].
|useInPregnancyAUS=* '''Australian Drug Evaluation Committee (ADEC) Pregnancy Category'''
|useInPregnancyAUS=* '''Australian Drug Evaluation Committee (ADEC) Pregnancy Category'''


There is no Australian Drug Evaluation Committee (ADEC) guidance on usage of {{PAGENAME}} in women who are pregnant.
There is no Australian Drug Evaluation Committee (ADEC) guidance on usage of {{PAGENAME}} in women who are pregnant.
|useInLaborDelivery=There is no FDA guidance on use of {{PAGENAME}} during labor and delivery.
|useInLaborDelivery=There is no FDA guidance on use of {{PAGENAME}} during labor and delivery.
|useInNursing=* Propylthiouracil is transferred to breasdt milk to a small extent and therefore likely results in clinically insignificant doses to the suckling infant. One one study, nine lactating women were administered 400 mg of propylthiouracil by mouth. The mean amount of propylthiouracil excreted during 4 hours after drug administration was 0.025% of the administered dose.
|useInNursing=* Propylthiouracil is transferred to [[breast|breasdt milk]] to a small extent and therefore likely results in clinically insignificant doses to the suckling infant. One one study, nine [[Breastfeeding|lactating]] women were administered 400 mg of propylthiouracil by mouth. The mean amount of propylthiouracil excreted during 4 hours after drug administration was 0.025% of the administered dose.
|useInPed=* Post-marketing reports of severe liver injury including hepatic failure requiring liver transplantation or resulting in death have been reported in the pediatric population. No such reports have been observed with methimazole. As such, propylthiouracil is not recommended for use in the pediatric population except in rare instances in which methimazole is not well-tolerated and surgery or radioactive iodine therapy are not appropriate.
|useInPed=* Post-marketing reports of [[Hepatic failure|severe liver injury]] including [[hepatic failure]] requiring liver transplantation or resulting in [[death]] have been reported in the [[pediatric]] population. No such reports have been observed with [[methimazole]]. As such, propylthiouracil is not recommended for use in the [[pediatric]] population except in rare instances in which [[methimazole]] is not well-tolerated and [[surgery]] or [[antithyroid agent|radioactive iodine therapy]] are not appropriate.


* When used in children, parents and patients should be informed of the risk of [[liver failure]]. If patients taking propylthiouracil develop tiredness, nausea, anorexia, fever, pharyngitis, or malaise, propylthiouracil should be discontinued immediately by the patient, a physician should be contacted, and a white blood cell count, liver function tests, and transaminase levels obtained.
* When used in children, parents and patients should be informed of the risk of [[liver failure]]. If patients taking propylthiouracil develop [[tiredness]], [[nausea]], [[anorexia]], [[fever]], [[pharyngitis]], or [[malaise]], propylthiouracil should be discontinued immediately by the patient, a physician should be contacted, and a [[white blood cell count]], [[liver function tests]], and [[transaminase]] levels obtained.
|useInGeri=There is no FDA guidance on the use of {{PAGENAME}} with respect to geriatric patients.
|useInGeri=There is no FDA guidance on the use of {{PAGENAME}} with respect to geriatric patients.
|useInGender=There is no FDA guidance on the use of {{PAGENAME}} with respect to specific gender populations.
|useInGender=There is no FDA guidance on the use of {{PAGENAME}} with respect to specific gender populations.
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<!--Administration and Monitoring-->
<!--Administration and Monitoring-->
|administration=* Oral
|administration=* [[Oral]]
|monitoring======Laboratory Tests=====
|monitoring======Laboratory Tests=====


* Because propylthiouracil may cause hypoprothrombinemia and bleeding, monitoring of prothrombin time should be considered during therapy with the drug, especially before surgical procedures.
* Because propylthiouracil may cause [[hypoprothrombinemia]] and bleeding, monitoring of [[prothrombin time]] should be considered during therapy with the drug, especially before [[surgical procedures]].


* Thyroid function tests should be monitored periodically during therapy. Once clinical evidence of [[hyperthyroidism]] has resolved, the finding of an elevated serum TSH indicates that a lower maintenance dose of propylthiouracil should be employed.
* [[Thyroid function tests]] should be monitored periodically during therapy. Once clinical evidence of [[hyperthyroidism]] has resolved, the finding of an elevated serum [[TSH]] indicates that a lower maintenance dose of propylthiouracil should be employed.
|IVCompat=There is limited information regarding <i>IV Compatibility</i> of {{PAGENAME}} in the drug label.
|IVCompat=There is limited information regarding <i>IV Compatibility</i> of {{PAGENAME}} in the drug label.


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|overdose======Signs and Symptoms=====
|overdose======Signs and Symptoms=====


* Nausea, vomiting, epigastric distress, headache, fever, arthralgia, pruritus, edema, and pancytopenia. Agranulocytosis is the most serious effect. Rarely, exfoliative dermatitis, hepatitis, neuropathies, or CNS stimulation or depression may occur.
* [[Nausea]], [[vomiting]], [[epigastric distress]], [[headache]], [[fever]], [[arthralgia]], [[pruritus]], [[edema]], and [[pancytopenia]]. [[Agranulocytosis]] is the most serious effect. Rarely, [[exfoliative dermatitis]], [[hepatitis]], [[neuropathies]], or [[CNS|CNS stimulation or depression]] may occur.


* No information is available on the following: LD50: concentration of propylthiouracil in biologic fluids associated with toxicity and/or death; the amount of drug in a single dose usually associated with symptoms of overdosage; or the amount of propylthiouracil in a single dose likely to be life-threatening.
* No information is available on the following: [[LD50]]: concentration of propylthiouracil in biologic fluids associated with [[toxicity]] and/or [[death]]; the amount of drug in a single dose usually associated with symptoms of [[overdosage]]; or the amount of propylthiouracil in a single dose likely to be life-threatening.


=====Treatment=====
=====Treatment=====


* To obtain up-to-date information about the treatment of overdose, a good resource is the certified Regional Poison Control Center. In managing overdosage, consider the possibility of multiple drug overdoses, interaction among drugs, and unusual drug kinetics in the patient.
* To obtain up-to-date information about the treatment of [[overdose]], a good resource is the certified Regional Poison Control Center. In managing [[overdosage]], consider the possibility of multiple [[drug overdoses]], [[interaction]] among drugs, and unusual [[kinetics|drug kinetics]] in the patient.


* In the event of an overdose, appropriate supportive treatment should be initiated as dictated by the patient's medical status.
* In the event of an overdose, appropriate supportive treatment should be initiated as dictated by the patient's medical status.
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| StdInChIKey = KNAHARQHSZJURB-UHFFFAOYSA-N
| StdInChIKey = KNAHARQHSZJURB-UHFFFAOYSA-N
}}
}}
|mechAction=* Propylthiouracil inhibits the synthesis of thyroid hormones. It inhibits the conversation of thyroxine to triiodothyronine to peripheral tissues and may therefore be an effective treatment for thyroid storm.
|mechAction=* Propylthiouracil inhibits the synthesis of [[thyroid hormones]]. It inhibits the conversation of [[thyroxine]] to [[triiodothyronine]] to peripheral tissues and may therefore be an effective treatment for [[thyroid storm]].
|structure=* Propylthiouracil (6-propyl-2-thiouracil) is one of the thiocarbamide compounds. It is a white, crystalline substance that has a bitter taste and is very slightly soluble in water.
|structure=* Propylthiouracil (6-propyl-2-[[thiouracil]]) is one of the [[thiocarbamide]] compounds. It is a white, [[crystalline]] substance that has a [[bitter taste]] and is very slightly [[soluble]] in water.


* Propylthiouracil is an antithyroid drug administered orally. The structural formula is:
* Propylthiouracil is an [[antithyroid agents|antithyroid drug]] administered orally. The [[structural formula]] is:


[[File:Propylthiouracil structure.png|400px|This image is provided by the National Library of Medicine.]]
[[File:Propylthiouracil structure.png|400px|This image is provided by the National Library of Medicine.]]
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<!--Pharmacokinetics-->
<!--Pharmacokinetics-->
|PK=* Propylthiouracil inhibits the synthesis of thyroid hormones and thus is effective in the treatment of [[hyperthyroidism]]. The drug does not inactivate existing thyroxine and triodothyronine that are stored in the thyroid or circulating in the blood, nor does it interfere with the effectiveness of thyroid hormones given by mouth or by injection. Propylthiouracil inhibits the conversation of thyroxine to triiodothyronine to peripheral tissues and may therefore be an effective treatment for thyroid storm.
|PK=* Propylthiouracil inhibits the synthesis of [[thyroid hormones]] and thus is effective in the treatment of [[hyperthyroidism]]. The drug does not inactivate existing [[thyroxine]] and [[triodothyronine]] that are stored in the [[thyroid]] or circulating in the [[blood]], nor does it interfere with the effectiveness of [[thyroid hormones]] given by mouth or by injection. Propylthiouracil inhibits the conversation of [[thyroxine]] to [[triiodothyronine]] to peripheral tissues and may therefore be an effective treatment for [[thyroid storm]].


* Propylthiouracil is readily absorbed and is extensively metabolized. Approximately 35% of the drug is excreted in the urine, in intact and in conjugated forms, within 24 hours.
* Propylthiouracil is readily absorbed and is extensively [[metabolized]]. Approximately 35% of the drug is [[excreted]] in the [[urine]], in intact and in conjugated forms, within 24 hours.
|nonClinToxic=There is limited information regarding <i>Nonclinical Toxicology</i> of {{PAGENAME}} in the drug label.
|nonClinToxic=There is limited information regarding <i>Nonclinical Toxicology</i> of {{PAGENAME}} in the drug label.


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|clinicalStudies======Carcinogenesis, Mutagenesis, Impairment of Fertility=====
|clinicalStudies======Carcinogenesis, Mutagenesis, Impairment of Fertility=====


* Laboratory animals treated with propylthiouracil for > 1 year have demonstrated thyroid hyperplasia and carcinoma formation1. Such animal findings are seen with continuous suppression of thyroid function by sufficient doses of a variety of antithyroid agents, as well as in dietary iodine deficiency, subtotal thyroidectomy, and implantation of autonomous thyrotropic hormone - secreting pituitary tumors. Pituitary adenomas have also been described.
* Laboratory animals treated with propylthiouracil for > 1 year have demonstrated [[Thyroid disease|thyroid hyperplasia]] and [[carcinoma]] formation1. Such animal findings are seen with continuous suppression of [[thyroid function test|thyroid function]] by sufficient doses of a variety of [[antithyroid agents]], as well as in [[Iodine deficiency|dietary iodine deficiency]], [[Thyroidectomy|subtotal thyroidectomy]], and implantation of [[Thyrotropin-releasing hormone|autonomous thyrotropic hormone]] - [[pituitary tumors|secreting pituitary tumors]]. [[Pituitary adenomas]] have also been described.
|howSupplied=Propylthiouracil Tablets, USP, 50 mg: White, Round, Scored Tablet, Debossed “West-ward 480”.
|howSupplied=Propylthiouracil Tablets, USP, 50 mg: White, Round, Scored Tablet, Debossed “West-ward 480”.


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|fdaPatientInfo=Patients should be advised that if they become pregnant or intend to become pregnant white taking an antithyroid drug, they should contact their physician immediately about their therapy.
|fdaPatientInfo=Patients should be advised that if they become pregnant or intend to become pregnant white taking an antithyroid drug, they should contact their physician immediately about their therapy.


Patients should report immediately any evidence of illness, particularly sore throat, skin eruptions, fever, headache, or general malaise. They also should report symptoms suggestive of hepatic dysfunction (anorexia, pruritis, right upper quadrant pain, etc).
Patients should report immediately any evidence of illness, particularly [[sore throat]], [[skin eruptions]], [[fever]], [[headache]], or general [[malaise]]. They also should report symptoms suggestive of [[hepatic dysfunction]] ([[anorexia]], [[pruritis]], [[right upper quadrant pain]], etc).
|alcohol=* Alcohol-{{PAGENAME}} interaction has not been established. Talk to your doctor about the effects of taking alcohol with this medication.
|alcohol=* Alcohol-{{PAGENAME}} interaction has not been established. Talk to your doctor about the effects of taking alcohol with this medication.


Latest revision as of 17:01, 20 August 2015

Propylthiouracil
Black Box Warning
Adult Indications & Dosage
Pediatric Indications & Dosage
Contraindications
Warnings & Precautions
Adverse Reactions
Drug Interactions
Use in Specific Populations
Administration & Monitoring
Overdosage
Pharmacology
Clinical Studies
How Supplied
Images
Patient Counseling Information
Precautions with Alcohol
Brand Names
Look-Alike Names

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Adeel Jamil, M.D. [2]

Disclaimer

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Black Box Warning

WARNING
See full prescribing information for complete Boxed Warning.
* Severe liver injury and acute liver failure, in some cases fatal, have been reported in patients treated with propylthiouracil. These reports of hepatic reactions include cases requiring liver transplantation in adult and pediatric patients.
  • Propylthiouracil should be reserved for patients who can not tolerate methimazole and in whom radioactive iodine therapy or surgery are not appropriate treatments for the management of hyperthyroidism.
  • Because of the risk of fetal abnormalities associated with methimazole, proplythiouracil may be the treatment of choice when an antithyroid drug is indicated during or just prior to the first trimester of pregnancy.

Overview

Propylthiouracil is a thyroid hormone antagonist and anti thyroide drug that is FDA approved for the treatment of Graves' disease with hyperthyroidism or toxic multinodular goiter, and to ameliorate symptoms of [[hyperthyroidism]] in preparation for thyroidectomy. There is a Black Box Warning for this drug as shown here. Common adverse reactions include nausea, vomiting, epigastric distress, loss of taste, arthralgia, paresthesias, myalgia, headache, drowsiness, pruritus, skin rash and urticaria.

Adult Indications and Dosage

FDA-Labeled Indications and Dosage (Adult)

  • Propylthiouracil is indicated:
  • in patients with Graves' disease with hyperthyroidism or toxic multinodular goiter who are intolerant of methimazole and for whom surgery or radioactive iodine therapy is not an appropriate treatment option.
  • to ameliorate symptoms of hyperthyroidism in preparation for thyroidectomy or radioactive iodine therapy in patients who are intolerant of methimazole.

Dosing Information

  • Propylthiouracil is administered orally. The total daily dosage is usually given in 3 equal doses at approximately 8-hour intervals.
Adults
  • The initial dose is 300 mg daily. In patients with severe hyperthyroidism, very large goiters, or both, the initial dose may be increased to 400 mg daily; an occasional patient will require 400 to 900 mg daily initially. The usual maintenance dose is 100 to 150 mg daily. 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.
Geriatric Use
  • Clinical studies of propylthiouracil did not include sufficient numbers of subjects aged 65 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.

Off-Label Use and Dosage (Adult)

Guideline-Supported Use

There is limited information regarding Off-Label Guideline-Supported Use of Propylthiouracil in adult patients.

Non–Guideline-Supported Use

There is limited information regarding Off-Label Non–Guideline-Supported Use of Propylthiouracil in adult patients.

Pediatric Indications and Dosage

FDA-Labeled Indications and Dosage (Pediatric)

  • Propylthiouracil is generally not recommended for use in the pediatric patient population except in rare instances in which other alternative therapies are not appropriate options. Studies evaluating appropriate dosing regimen have not been conducted in the pediatric population although general practice would suggest initiation of therapy in patients 6 years or older at a dosage of 50 mg daily with careful upward titration based on clinical response and evaluation of TSH and free T4 levels. Although cases of severe liver injury have been reported with doses as low as 50 mg/day, most cases were associated with doses of 300 mg/day and higher.

Off-Label Use and Dosage (Pediatric)

Guideline-Supported Use

There is limited information regarding Off-Label Guideline-Supported Use of Propylthiouracil in pediatric patients.

Non–Guideline-Supported Use

There is limited information regarding Off-Label Non–Guideline-Supported Use of Propylthiouracil in pediatric patients.

Contraindications

Warnings

WARNING
See full prescribing information for complete Boxed Warning.
* Severe liver injury and acute liver failure, in some cases fatal, have been reported in patients treated with propylthiouracil. These reports of hepatic reactions include cases requiring liver transplantation in adult and pediatric patients.
  • Propylthiouracil should be reserved for patients who can not tolerate methimazole and in whom radioactive iodine therapy or surgery are not appropriate treatments for the management of hyperthyroidism.
  • Because of the risk of fetal abnormalities associated with methimazole, proplythiouracil may be the treatment of choice when an antithyroid drug is indicated during or just prior to the first trimester of pregnancy.

Liver Toxicity

Agranulocytosis
Hypothyroidism

PRECAUTIONS

General

Adverse Reactions

Clinical Trials Experience

  • To report SUSPECTED ADVERSE REACTIONS, contact West-ward Pharmaceutical Corp. at 1-877-233-2001 or the FDA at 1-800-FDA-1088 or WWW.FDA.GOV/MEDWATCH.

Postmarketing Experience

There is limited information regarding Postmarketing Experience of Propylthiouracil in the drug label.

Drug Interactions

Anticoagulants (oral)=

Beta-adrenergic blocking agents
Digitalis Glycosides
Theophylline

Use in Specific Populations

Pregnancy

Pregnancy Category (FDA): D


Pregnancy Category (AUS):

  • Australian Drug Evaluation Committee (ADEC) Pregnancy Category

There is no Australian Drug Evaluation Committee (ADEC) guidance on usage of Propylthiouracil in women who are pregnant.

Labor and Delivery

There is no FDA guidance on use of Propylthiouracil during labor and delivery.

Nursing Mothers

  • Propylthiouracil is transferred to breasdt milk to a small extent and therefore likely results in clinically insignificant doses to the suckling infant. One one study, nine lactating women were administered 400 mg of propylthiouracil by mouth. The mean amount of propylthiouracil excreted during 4 hours after drug administration was 0.025% of the administered dose.

Pediatric Use

Geriatic Use

There is no FDA guidance on the use of Propylthiouracil with respect to geriatric patients.

Gender

There is no FDA guidance on the use of Propylthiouracil with respect to specific gender populations.

Race

There is no FDA guidance on the use of Propylthiouracil with respect to specific racial populations.

Renal Impairment

There is no FDA guidance on the use of Propylthiouracil in patients with renal impairment.

Hepatic Impairment

There is no FDA guidance on the use of Propylthiouracil in patients with hepatic impairment.

Females of Reproductive Potential and Males

There is no FDA guidance on the use of Propylthiouracil in women of reproductive potentials and males.

Immunocompromised Patients

There is no FDA guidance one the use of Propylthiouracil in patients who are immunocompromised.

Administration and Monitoring

Administration

Monitoring

Laboratory Tests
  • Thyroid function tests should be monitored periodically during therapy. Once clinical evidence of hyperthyroidism has resolved, the finding of an elevated serum TSH indicates that a lower maintenance dose of propylthiouracil should be employed.

IV Compatibility

There is limited information regarding IV Compatibility of Propylthiouracil in the drug label.

Overdosage

Signs and Symptoms
  • No information is available on the following: LD50: concentration of propylthiouracil in biologic fluids associated with toxicity and/or death; the amount of drug in a single dose usually associated with symptoms of overdosage; or the amount of propylthiouracil in a single dose likely to be life-threatening.
Treatment
  • In the event of an overdose, appropriate supportive treatment should be initiated as dictated by the patient's medical status.

Pharmacology

Propylthiouracil
Clinical data
AHFS/Drugs.comMonograph
MedlinePlusa682465
Pregnancy
category
  • D
Routes of
administration		Oral
ATC code
Legal status
Legal status
  • In general: ℞ (Prescription only)
Pharmacokinetic data
Bioavailability80%-95%
Metabolism?
Elimination half-life2 hours
Excretion?
Identifiers
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
E number{{#property:P628}}
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Chemical and physical data
FormulaC7H10N2OS
Molar mass170.233 g/mol
3D model (JSmol)
  (verify)

Mechanism of Action

Structure

This image is provided by the National Library of Medicine.

Pharmacodynamics

There is limited information regarding Pharmacodynamics of Propylthiouracil in the drug label.

Pharmacokinetics

  • Propylthiouracil is readily absorbed and is extensively metabolized. Approximately 35% of the drug is excreted in the urine, in intact and in conjugated forms, within 24 hours.

Nonclinical Toxicology

There is limited information regarding Nonclinical Toxicology of Propylthiouracil in the drug label.

Clinical Studies

Carcinogenesis, Mutagenesis, Impairment of Fertility

How Supplied

Propylthiouracil Tablets, USP, 50 mg: White, Round, Scored Tablet, Debossed “West-ward 480”.

Bottles of 100 tablets.

Bottles of 1000 tablets.

Unit Dose Boxes of 100 tablets.

Dispense in a tight, light-resistant container as defined in the USP using a child-resistant closure.

Reference:

International Agency for Research on Cancer, IARC Monographs on the Evaluation of the Carcinogenic Risk of Chemicals to Man. 1974; 7:67-76.

Manufactured By: West-ward Pharmaceutical Corp. Eatontown, NJ 07724 Revised August 2011

Storage

  • Store at 20-25°C (68-77°F) [See USP Controlled Room Temperature]. Protect from light and moisture.

Images

Drug Images

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Package and Label Display Panel

Propylthiouracil Tablets, USP

50 mg

100 Tablets

NDC 0143-1480-01 {{#ask: Label Page::Propylthiouracil |?Label Name |format=template |template=DrugLabelImages |mainlabel=- |sort=Label Page }}

Patient Counseling Information

Patients should be advised that if they become pregnant or intend to become pregnant white taking an antithyroid drug, they should contact their physician immediately about their therapy.

Patients should report immediately any evidence of illness, particularly sore throat, skin eruptions, fever, headache, or general malaise. They also should report symptoms suggestive of hepatic dysfunction (anorexia, pruritis, right upper quadrant pain, etc).

Precautions with Alcohol

  • Alcohol-Propylthiouracil interaction has not been established. Talk to your doctor about the effects of taking alcohol with this medication.

Brand Names

There is limited information regarding Propylthiouracil Brand Names in the drug label.

Look-Alike Drug Names

There is limited information regarding Propylthiouracil Look-Alike Drug Names in the drug label.

Drug Shortage Status

Price

References

The contents of this FDA label are provided by the National Library of Medicine.

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