Friday, September 23, 2016

Progesterone



Class: Progestins
ATC Class: G03DA04
VA Class: HS800
CAS Number: 57-83-0
Brands: Crinone, Endometrin, Prometrium

Introduction

Naturally occurring progestin.103 105 a


Uses for Progesterone


Amenorrhea


Treatment of secondary amenorrhea.101 102 103 105


Assisted Reproductive Technology


Used to support embryo implantation and early pregnancy as part of assisted reproductive technology (ART) treatment of infertile women.104 105 106


Prevention of Endometrial Changes Associated with Estrogens


Reduction of the incidence of endometrial hyperplasia and the attendant risk of endometrial carcinoma in postmenopausal women receiving estrogen replacement therapy.103


Uterine Bleeding


Treatment of abnormal uterine bleeding due to hormonal imbalance in the absence of organic pathology such as fibroids or uterine cancer.101 102


Progesterone Dosage and Administration


Administration


Administer orally, parenterally, or intravaginally as a gel or insert.101 102 103 104 105


Oral Administration


Administer once daily at bedtime.103 Administration at bedtime may alleviate some adverse effects (e.g., dizziness, blurred vision).103


If difficulty swallowing the capsule is experienced, administer in an upright position with adequate amounts of fluid (e.g., a glass of water).103


IM Administration


Administer by IM injection.101 102


Vaginal Administration


Progesterone vaginal gel (Crinone): Administer intravaginally every other day, every day, or twice daily.105 Do not administer concurrently with other vaginal preparations.105 If therapy with another agent administered intravaginally is needed, administer the other agent 6 hours before or after progesterone vaginal gel.105


Progesterone vaginal insert (Endometrin): Administer intravaginally 2–3 times daily.104 Concomitant use with other preparations administered intravaginally is not recommended.104


Dosage


Individualize dosage according to the condition being treated and therapeutic response of the patient.101 102 103 104 105


Progesterone 4% vaginal gel (Crinone): Each prefilled applicator delivers approximately 1.125 g of gel (45 mg of progesterone).105


Progesterone 8% vaginal gel (Crinone): Each prefilled applicator delivers approximately 1.125 g of gel (90 mg of progesterone).105


Progesterone vaginal insert (Endometrin): Appropriate dose for women ≥35 years of age not established.104


Adults


Amenorrhea

Oral

400 mg daily for 10 days.103


IM

5–10 mg daily for 6–8 consecutive days.101 102


Withdrawal bleeding usually occurs within 48–72 hours after discontinuing therapy.101 102 Spontaneous normal cycles may occur in some patients after a single course of therapy.101 102


Vaginal

Progesterone 4% vaginal gel (Crinone): Administer contents of one prefilled applicator every other day for a total of 6 doses.105


For patients who do not respond to the 4% gel, administer the contents of one prefilled applicator of progesterone 8% vaginal gel (Crinone) every other day for a total of 6 doses.105 Women who require the higher dose should receive Crinone 8% vaginal gel; increasing the volume of the 4% gel will not achieve the same progesterone concentrations as the 8% gel.105


Assisted Reproductive Technology

Progesterone Supplementation/Replacement

Vaginal

Progesterone 8% vaginal gel (Crinone): For women who require progesterone supplementation, administer contents of one prefilled applicator once daily.105 If pregnancy occurs, continue until placenta autonomy is achieved, up to 10–12 weeks.105


Progesterone 8% vaginal gel (Crinone): For women who require progesterone replacement, administer contents of one prefilled applicator twice daily.105 If pregnancy occurs, continue until placenta autonomy is achieved, up to 10–12 weeks.105


Progesterone vaginal insert (Endometrin): One insert 2–3 times daily.104 Start at oocyte retrieval; continue for up to 10 weeks.104


Prevention of Endometrial Changes Associated with Estrogens

Oral

200 mg daily for 12 continuous days per 28-day cycle.103


Uterine Bleeding

IM

5–10 mg daily for 6 days.101 102 When used concomitantly with estrogen therapy, initiate progesterone therapy after 2 weeks of estrogen therapy.101 102 Discontinue progesterone if menses occurs during the series of injections.101 102


Cautions for Progesterone


Contraindications



  • Undiagnosed vaginal bleeding.101 102 103 105




  • Known or suspected breast or genital cancer; history of breast cancer.101 102 103 104 105




  • Active DVT or pulmonary embolism; history of DVT or pulmonary embolism.103




  • Active or recent arterial thromboembolic disease (e.g., stroke, MI), thrombophlebitis, or cerebral apoplexy.101 102 103 104 105




  • Liver disease or dysfunction.101 102 103 104 105




  • Missed abortion or ectopic pregnancy.101 102 104 105




  • Use as a pregnancy test.101




  • Progesterone capsules are contraindicated in pregnant women and those with suspected pregnancy.103 Not effective for any purpose during pregnancy.103




  • Known hypersensitivity to progesterone or any ingredient in the formulation.101 102 103 104 105




  • Progesterone capsules (Prometrium): Known hypersensitivity to peanuts because the capsules contain peanut oil.103



Warnings/Precautions


Warnings


Cardiovascular or Cerebrovascular Disorders

Possible cardiac disorders (MI) or thromboembolic and thrombotic disorders (e.g., thrombophlebitis, pulmonary embolism, cerebrovascular disorders, retinal thrombosis).101 102 103 104 105 Observe patients for these effects; discontinue immediately and do not readminister if these disorders occur or are suspected.101 102 103 104 105 (See Contraindications under Cautions.)


Progesterone capsules (Prometrium): Syncope and hypotension reported.103


Ocular Effects

If unexplained, sudden or gradual, partial or complete loss of vision; proptosis or diplopia; papilledema; migraine; or retinal vascular lesions occur, discontinue and initiate appropriate diagnostic and therapeutic measures.101 102 103 Do not reinitiate therapy if ocular examination reveals evidence of papilledema or retinal vascular lesions.101 102 103


Sensitivity Reactions


Peanut Hypersensitivity

Progesterone capsules (Prometrium) contain peanut oil.103 Do not use in patients with peanut allergy.103 (See Contraindications under Cautions.)


General Precautions


Fluid Retention

May cause some degree of fluid retention.101 102 103 105 Use with caution and careful monitoring in patients with conditions (e.g., asthma, seizure disorders, migraine headache, cardiac or renal impairment) that might be aggravated by fluid retention.101 102 103 105


Bleeding Irregularities

Possible breakthrough or irregular vaginal bleeding.101 102 103 105 Perform adequate diagnostic tests in patients with undiagnosed vaginal bleeding.101 102 103 105


Depression

Possible depression.101 102 103 104 105 Exercise caution in women with a history of depression; discontinue if severe depression recurs during use.101 102 103 104 105


Physical Examination and Follow-up

Physical examination prior to initiation of therapy advised.101 102 103 105 Physical examination should include special attention to the breasts and pelvic organs and should include a Papanicolaou test (Pap smear) and relevant laboratory tests.101 102 103 105


Carcinoma of the Breast

Addition of progesterone to estrogen replacement therapy may increase the risk of breast cancer beyond that associated with estrogen use alone.103


Metabolic Effects

Possible adverse effects on carbohydrate and lipid metabolism.101 102 105 Monitor patients with hyperlipidemias or diabetes mellitus carefully.101 102 105


Prolonged Therapy

Effect of long-term therapy on pituitary, ovarian, adrenal, hepatic, or uterine function not determined.103


Climacteric

Onset of climacteric may be masked in women.101 102


Estrogen Therapy

When used in combination with an estrogen, consider the cautions, precautions, and contraindications associated with estrogens.103


CNS Effects

Progesterone capsules (Prometrium): Transient dizziness reported.103 Use caution when driving or operating machinery.103


Progesterone capsules (Prometrium): Extreme dizziness and/or drowsiness, blurred vision, slurred speech, difficulty walking, loss of consciousness, vertigo, confusion, disorientation, and shortness of breath reported; women who experience these adverse effects should consult their healthcare provider.103


Specific Populations


Pregnancy

Used to support embryo implantation and maintain pregnancy as a component of ART treatment in infertile women.104 105 106 Such use is associated with increased ongoing pregnancy rates.104 105 106


Progesterone capsules (Prometrium): Category B.103


Lactation

Progestins are distributed into milk.102 103 104 105 Caution advised.102 103 104 105


Pediatric Use

Safety and efficacy not established.102 103 104 105 Not indicated in pediatric patients.103 104


Adult Use

Vaginal inserts (Endometrin): Efficacy not established in women ≥35 years of age.104


Geriatric Use

Progesterone injection, vaginal inserts, and gel: Safety and efficacy not established in patients >65 years of age.102 104 105


Progesterone capsules (Prometrium): Insufficient experience in those ≥65 years of age to determine whether they respond differently than younger adults.103 Select dose with caution; start at the lower end of the dosing range due to the greater frequency of decreased hepatic, renal, and/or cardiac function and of concomitant disease and drug therapy.103


Hepatic Impairment

Contraindicated in patients with liver dysfunction or disease.101 102 103 104 105


Progesterone capsules (Prometrium): If indicated in patients with mild to moderate hepatic dysfunction, monitor patient closely.103


Renal Impairment

Progesterone injection and capsules: Safety and efficacy not established in patients with renal impairment.102 103 Use with caution; carefully monitor patients with renal impairment.103


Common Adverse Effects


Menstrual abnormalities (amenorrhea; breakthrough bleeding and/or spotting; changes in menstrual flow), weight changes, dizziness, headache, abdominal pain and/or distention, breast tenderness and/or pain, fatigue, musculoskeletal pain, joint pain.101 102 103 104 105


Injection site pain.101 102


Interactions for Progesterone


Drugs Affecting Hepatic Microsomal Enzymes


Pharmacokinetic interaction possible with drugs that are inhibitors of CYP3A4.103 104


Vaginal Preparations


Progesterone vaginal gel (Crinone): Do not administer concurrently with other vaginal preparations.105 If therapy with another agent administered intravaginally is needed, administer the other agent 6 hours before or after progesterone vaginal gel.105


Progesterone vaginal insert (Endometrin): Concomitant administration with another vaginal preparation may alter release and absorption of progesterone.104 Concomitant use with other preparations administered intravaginally is not recommended.104


Specific Drugs









Drug



Interaction



Comments



Conjugated estrogens



Progesterone capsules: Decreased estradiol AUC, increased estrone and equilin AUCs103


Progesterone Pharmacokinetics


Absorption


Bioavailability


Rapidly absorbed from the GI tract; peak plasma concentrations achieved within 3 hours.103


Peak plasma concentrations attained in 8–9 hours following IM administration.102 105


Peak plasma concentrations attained in 5–7 hours following administration of progesterone vaginal gel.105 Absorption is prolonged due to sustained-release properties of this preparation.105


Peak plasma concentrations reached in 17–24 hours following administration of progesterone vaginal insert.104


Food


Food increases bioavailability of progesterone capsules.103


Distribution


Extent


Distributed into human milk.102 103 104 105


Plasma Protein Binding


96–99% (mainly albumin).103 104 105


Elimination


Metabolism


Metabolized in the liver to pregnanediols and pregnanolones, followed by glucuronide and sulfate conjugation.102 103 104 Further metabolism may occur in the GI tract.104


Elimination Route


Excreted in urine and bile, mainly as metabolites.102 103 104


Following administration of progesterone injection, 50-60% of metabolites are excreted by the kidneys, while approximately 10% are excreted by the bile and feces.104 105 A small portion is excreted in the bile unchanged.104 105


Half-life


IM doses: 20–30 hours.105


Vaginal gel: 30–60 hours.105


Stability


Storage


Oral


Capsules

Tight, light-resistant containers at 25°C (may be exposed to 15–30°C).103


Parenteral


Injection

15–30°C.102


Vaginal


Gel and Inserts

25°C (may be exposed to 15–30°C).104 105


ActionsActions



  • Formed from steroid precursors in the ovary, testis, adrenal cortex, and placenta; secreted mainly from the corpus luteum of the ovary during the latter half of the menstrual cycle.a




  • Required for implantation of the ovum and for maintenance of pregnancy.a




  • Transforms a proliferative endometrium into a secretory one.a




  • Stimulates growth of mammary alveolar tissue and relaxes uterine smooth muscle.a




  • Minimal estrogenic and androgenic activity.a



Advice to Patients



  • Importance of reading the manufacturer's patient information.102 103 104 105




  • Importance of advising patients of anticipated menstrual effects.102 103




  • Progesterone capsules (Prometrium): Importance of using caution when driving or operating machinery, especially during the initiation of therapy.103




  • Progesterone vaginal gel (Crinone): Importance of following special instructions if the gel is used at altitudes >2500 feet.105




  • Importance of discontinuing therapy and contacting clinician if sudden partial or complete vision loss, blurred vision, bulging of the eyes, double vision, or migraine occur.101 102 103 104 105




  • Importance of discontinuing therapy and contacting clinician if any symptoms of thromboembolic and thrombotic disorders occurs.101 102 103 104 105




  • Importance of women informing clinicians if they are or plan to become pregnant or plan to breast-feed.101 102 103




  • Importance of informing clinicians of existing or contemplated concomitant therapy, including prescription and OTC drugs, as well as concomitant illnesses.101 102 103 104 105




  • Advise women using the vaginal gel or insert not to use other vaginal preparations.104 105 If therapy with another agent administered intravaginally is needed in a women using the gel, administer the other agent 6 hours before or after progesterone vaginal gel.105




  • Importance of informing patients of other important precautionary information.101 102 103 104 105 (See Cautions.)



Preparations


Excipients in commercially available drug preparations may have clinically important effects in some individuals; consult specific product labeling for details.


* available from one or more manufacturer, distributor, and/or repackager by generic (nonproprietary) name











































Progesterone

Routes



Dosage Forms



Strengths



Brand Names



Manufacturer



Bulk



Powder



Progesterone Powder Micronized or Microcrystalline for Prescription Compounding



Paddock, X-Gen



Oral



Capsules



100 mg



Prometrium (with peanut oil)



Solvay



200 mg



Prometrium (with peanut oil)



Solvay



Parenteral



Injection



50 mg/mL*



Progesterone Injection (with benzyl alcohol 10% and sesame oil)



Abraxis, Watson



Vaginal



Gel



4%



Crinone (available in prefilled, disposable applicators)



Columbia



8%



Crinone (available in prefilled, disposable applicators)



Columbia



Insert



100 mg



Endometrin (with disposable applicators)



Ferring


Comparative Pricing


This pricing information is subject to change at the sole discretion of DS Pharmacy. This pricing information was updated 03/2011. Actual costs to patients will vary depending on the use of specific retail or mail-order locations and health insurance copays.


Prochieve 4% Gel (WATSON LABS): 26/$159.99 or 78/$454.98


Prochieve 8% Gel (WATSON LABS): 26/$221 or 78/$660.93


Progesterone 50MG/ML Oil (WATSON LABS): 10/$37.99 or 30/$105.97


Prometrium 100MG Capsules (ABBOTT): 30/$68.99 or 90/$184.98


Prometrium 200MG Capsules (ABBOTT): 30/$121.99 or 90/$335.97



Disclaimer

This report on medications is for your information only, and is not considered individual patient advice. Because of the changing nature of drug information, please consult your physician or pharmacist about specific clinical use.


The American Society of Health-System Pharmacists, Inc. and Drugs.com represent that the information provided hereunder was formulated with a reasonable standard of care, and in conformity with professional standards in the field. The American Society of Health-System Pharmacists, Inc. and Drugs.com make no representations or warranties, express or implied, including, but not limited to, any implied warranty of merchantability and/or fitness for a particular purpose, with respect to such information and specifically disclaims all such warranties. Users are advised that decisions regarding drug therapy are complex medical decisions requiring the independent, informed decision of an appropriate health care professional, and the information is provided for informational purposes only. The entire monograph for a drug should be reviewed for a thorough understanding of the drug's actions, uses and side effects. The American Society of Health-System Pharmacists, Inc. and Drugs.com do not endorse or recommend the use of any drug. The information is not a substitute for medical care.

AHFS Drug Information. © Copyright, 1959-2011, Selected Revisions April 2008. American Society of Health-System Pharmacists, Inc., 7272 Wisconsin Avenue, Bethesda, Maryland 20814.




References



101. Abraxis Pharmaceutical Products, Inc. Progesterone injection prescribing information. Schaumburg, IL; 2006 Jun.



102. Watson Laboratories. Progesterone injection prescribing information. Corona, CA; 2007 Jan.



103. Solvay Pharmaceuticals, Inc. Prometrium(progesterone) capsule prescribing information. Marietta, GA; 2004 Dec.



104. Ferring Pharmaceuticals, Inc. Endometrin(progesterone) vaginal insert prescribing information. Suffern, NY; Jun 2007.



105. Columbia Laboratories, Inc. Crinone (progesterone) bioadhesive vaginal gel prescribing information. Livingston, NJ; 2006 Dec.



106. Daya S, Gunby J. Luteal phase support in assisted reproductive cycles. Cochrane Database of Systematic Reviews. 2004, Issue 3. Art. no.:CD004830. DOI: 10.1002/14651858. CD004830.



a. AHFS Drug Information 2007. McEvoy GK, ed. Progesterone. Bethesda, MD: American Society of Health-System Pharmacists; 2007: 3237-3238.



More Progesterone resources


  • Progesterone Side Effects (in more detail)
  • Progesterone Use in Pregnancy & Breastfeeding
  • Progesterone Drug Interactions
  • Progesterone Support Group
  • 15 Reviews for Progesterone - Add your own review/rating


  • Progesterone Natural MedFacts for Professionals (Wolters Kluwer)

  • Progesterone Professional Patient Advice (Wolters Kluwer)

  • Progesterone Prescribing Information (FDA)

  • Progesterone MedFacts Consumer Leaflet (Wolters Kluwer)

  • progesterone Advanced Consumer (Micromedex) - Includes Dosage Information

  • Crinone Gel MedFacts Consumer Leaflet (Wolters Kluwer)

  • Crinone Advanced Consumer (Micromedex) - Includes Dosage Information

  • Crinone Prescribing Information (FDA)

  • Endometrin Consumer Overview

  • Endometrin Insert MedFacts Consumer Leaflet (Wolters Kluwer)

  • Endometrin Prescribing Information (FDA)

  • Prochieve Prescribing Information (FDA)

  • Prochieve Gel MedFacts Consumer Leaflet (Wolters Kluwer)

  • Prometrium Prescribing Information (FDA)



Compare Progesterone with other medications


  • Amenorrhea
  • Endometrial Hyperplasia, Prophylaxis
  • Perimenopausal Symptoms
  • Premature Labor
  • Progesterone Insufficiency
  • Seizures
  • Uterine Bleeding

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