ﺑﺎﺯﮔﺸﺖ ﺑﻪ ﺻﻔﺤﻪ ﻗﺒﻠﯽ
خرید پکیج
تعداد آیتم قابل مشاهده باقیمانده : 3 مورد
نسخه الکترونیک
medimedia.ir

Progesterone: Drug information

Progesterone: Drug information
2024© UpToDate, Inc. and its affiliates and/or licensors. All Rights Reserved.
For additional information see "Progesterone: Patient drug information"

For abbreviations, symbols, and age group definitions show table
ALERT: US Boxed Warning
Cardiovascular disorders (capsule):

Estrogens plus progestin therapy should not be used for the prevention of cardiovascular disease. The Women's Health Initiative (WHI) estrogen plus progestin substudy reported increased risks of deep vein thrombosis (DVT), pulmonary embolism (PE), stroke, and myocardial infarction (MI) in postmenopausal women (50 to 79 years of age) during 5.6 years of treatment with daily oral conjugated estrogens 0.625 mg combined with medroxyprogesterone 2.5 mg relative to placebo.

Probable dementia (capsule):

Estrogens plus progestin therapy should not be used for the prevention of dementia. The Women's Health Initiative Memory Study (WHIMS) estrogen plus progestin ancillary study of the WHI reported an increased risk of developing probable dementia in postmenopausal women 65 years and older during 4 years of treatment with daily conjugated estrogens 0.625 mg combined with medroxyprogesterone 2.5 mg, relative to placebo. It is unknown whether this finding applies to younger postmenopausal women.

Breast cancer (capsule):

The WHI estrogen plus progestin substudy also demonstrated an increased risk of invasive breast cancer.

Risks versus benefits (capsule):

In the absence of comparable data, assume these risks to be similar for other doses of conjugated estrogens and medroxyprogesterone and other combinations and dosage forms of estrogens and progestins. Prescribe progestins with estrogens at the lowest effective doses and for the shortest duration consistent with treatment goals and risks for the individual woman.

Brand Names: US
  • Crinone;
  • Endometrin;
  • Prometrium
Brand Names: Canada
  • ACT Progesterone;
  • AURO-Progesterone;
  • Crinone;
  • Endometrin;
  • PMS-Progesterone;
  • Prometrium;
  • REDDY-Progesterone;
  • TEVA-Progesterone
Pharmacologic Category
  • Progestin
Dosing: Adult
Abnormal uterine bleeding

Abnormal uterine bleeding:

IM: 5 to 10 mg/day for 6 doses. Start 2 weeks after estrogen therapy (if also being used). Bleeding should cease within 6 days. Discontinue use if menstrual flow begins during therapy.

Oral (off label): 200 mg once daily for the first 12 days of each month (Ref).

Assisted reproductive technology, luteal phase support

Assisted reproductive technology, luteal phase support: Note: Multiple regimens are available; data are insufficient regarding the most effective route of administration and dose (Ref).

IM (off label): 50 to 100 mg once daily (Ref).

Combination regimen: 50 mg IM on day 1, then every third day in combination with vaginal progesterone continued until estimated gestational age of 10 weeks. Frozen embryo transfer occurs on day 5, after 9 doses of vaginal progesterone and 2 doses of IM progesterone (Ref).

Intravaginal :

Capsule (off-label route, dose): 200 mg 3 times daily starting the day of oocyte retrieval and continuing for up to 12 weeks' gestation (Ref).

Gel (8%): 90 mg once daily. In patients with partial or complete ovarian failure, use 90 mg twice daily. If pregnancy occurs, may continue treatment for up to 10 to 12 weeks.

Insert: 100 mg 2 to 3 times daily starting the day after oocyte retrieval and continuing for up to 10 weeks.

Combination regimen (off-label dose): 200 mg twice daily in combination with IM progesterone continued until estimated gestational age of 10 weeks. Frozen embryo transfer occurs on day 5, after 9 doses of vaginal progesterone and 2 doses of IM progesterone (Ref).

Estrogen therapy-associated endometrial hyperplasia, prevention

Estrogen therapy-associated endometrial hyperplasia, prevention:

Note: Indicated in patients with a uterus receiving estrogen therapy (eg, for vasomotor symptoms associated with menopause or secondary amenorrhea). May be administered either cyclically (preferred in late menopausal transition and early postmenopause or functional hypothalamic amenorrhea) or continuously (preferred if >2 to 3 years postmenopause) (Ref). Discontinue when estrogen therapy is discontinued.

Oral: 200 mg once daily for 12 days each month (Ref) or 100 mg daily continuously (Ref).

Intravaginal (gel) (alternative agent): Note: Dosing is based on manufacturer’s labeling; however, intravaginal gel route of administration is considered nonpreferred to oral and is infrequently used due to limited data.

45 mg (4% gel) every other day for up to a total of 6 doses; if response is inadequate, may increase to 90 mg (8% gel) at same schedule (Ref).

Secondary amenorrhea, diagnostic aid

Secondary amenorrhea, diagnostic aid ("progesterone challenge"):

Oral: 200 mg daily for 10 days (Ref). Note: Withdrawal bleeding may be expected during therapy or within 7 days after cessation of therapy; absence of withdrawal bleeding suggests low endometrial estrogen exposure and/or uterine or outflow tract abnormality (Ref).

Manufacturer’s labeling: 400 mg once daily at bedtime for 10 days. Note: Higher oral doses (ie, >200 mg/day) are not preferred and infrequently used due to limited data.

IM (alternative agent): Note: Dosing is based on the manufacturer’s labeling; however, IM route of administration is considered nonpreferred to oral and is infrequently used.

5 to 10 mg/day for 6 to 8 consecutive days.

Spontaneous preterm birth, prevention

Spontaneous preterm birth, prevention (off-label use): Note: For use in patients with a singleton pregnancy, no prior preterm birth, and a cervical length <25 mm; use may be considered for patients with a singleton pregnancy, prior preterm birth, and a cervical length <25 mm. Data are insufficient regarding the most effective formulation and dose (Ref).

Intravaginal (8% gel): 90 mg once daily (Ref). Dosage range: 90 to 200 mg once daily using the 8% vaginal gel, oral capsules administered intravaginally, or compounded vaginal suppositories (Ref). Progesterone is generally continued up to 34 to 36 weeks' gestation (Ref).

Dosing: Kidney Impairment: Adult

Injection, oral: There are no dosage adjustments provided in the manufacturer's labeling (has not been studied). Use with caution.

Intravaginal gel, insert: There are no dosage adjustments provided in the manufacturer's labeling.

Dosing: Hepatic Impairment: Adult

Use is contraindicated in hepatic impairment or disease.

Dosing: Older Adult

Refer to adult dosing.

Adverse Reactions (Significant): Considerations
Depression

Literature is inconclusive on an established association; however, depression and other mood disturbances are the most common reasons for discontinuation of progesterone-containing products (Ref). Severe depression and suicidal ideation risk is low (Ref).

Mechanism: Dose-related; not clearly established. Hypotheses include dysregulation of the active metabolite allopregnanolone (ALLO) through gene expression, rate-limiting enzymes, altered sensitivity, and/or receptor plasticity (Ref). Additionally, progesterone is highly lipophilic and easily penetrates the blood-brain barrier; in times of stress, progesterone is converted to cortisol leading to impaired emotional processing (Ref). Lastly, decreased serotonin levels resulting from progesterone-induced monoamine oxidase and/or GABA inhibition of glutamate may contribute to negative mood symptoms (Ref).

Risk factors:

• Low-dose products (Ref)

• Known and/or personal or family history of depression (Ref)

• Menopause or other hormonal transitions (eg, puberty, peripartum, perimenopause) (Ref)

Adverse Reactions

The following adverse drug reactions and incidences are derived from product labeling unless otherwise specified.

Intramuscular injection:

Frequency not defined:

Cardiovascular: Edema

Dermatologic: Acne vulgaris, allergic skin rash, alopecia, pruritus, skin rash, urticaria

Endocrine & metabolic: Amenorrhea, change in menstrual flow, galactorrhea not associated with childbirth, hirsutism, spotting, weight gain, weight loss

Gastrointestinal: Nausea

Genitourinary: Breakthrough bleeding, breast tenderness, cervical erosion, change in cervical secretions

Hepatic: Cholestatic jaundice

Hypersensitivity: Nonimmune anaphylaxis

Local: Erythema at injection site, irritation at injection site, pain at injection site

Nervous system: Depression, drowsiness, insomnia

Miscellaneous: Fever

Oral (percentages reported when used in combination with or cycled with conjugated estrogens):

>10%:

Gastrointestinal: Abdominal pain (20%), bloating (12%)

Genitourinary: Breast tenderness (27%), mastalgia (6% to 16%), urinary tract abnormality (11%)

Infection: Viral infection (12%)

Nervous system: Depression (19%) (table 1), dizziness (15% to 24%), headache (16% to 31%)

Progesterone: Adverse Reaction: Depression

Drug (Progesterone)

Placebo

Population

Dose

Dosage Form

Indication

Number of Patients (Progesterone)

Number of Patients (Placebo)

19%

12%

Postmenopausal females

200 mg daily (12 days per calendar month cycle) with conjugated estrogens 0.625 mg

Oral capsules

Prevention of endometrial hyperplasia

178

174

Neuromuscular & skeletal: Musculoskeletal pain (12%)

1% to 10%:

Cardiovascular: Chest pain (7%)

Gastrointestinal: Cholecystectomy (2%), constipation (3%), diarrhea (7% to 8%), nausea and vomiting (≤8%)

Genitourinary: Breast carcinoma (2%), vaginal discharge (10%)

Nervous system: Anxiety (8%), fatigue (8%), irritability (8%)

Respiratory: Cough (8%)

Frequency not defined:

Cardiovascular: Acute myocardial infarction, deep vein thrombosis, pulmonary embolism

Nervous system: Cerebrovascular accident, dementia

Vaginal gel (percentages reported with assisted reproductive technology):

>10%:

Gastrointestinal: Abdominal pain (12%), constipation (27%), nausea (7% to 22%)

Genitourinary: Breast hypertrophy (40%), mastalgia (13%), nocturia (13%), perineal pain (17%)

Nervous system: Depression (11%), drowsiness (27%), headache (13% to 17%), nervousness (16%)

Neuromuscular & skeletal: Muscle cramps (15%)

1% to 10%:

Endocrine & metabolic: Decreased libido (10%)

Gastrointestinal: Bloating (7%), diarrhea (8%), vomiting (5%)

Genitourinary: Dyspareunia (6%), genital candidiasis (5%), vaginal discharge (7%), vulvovaginal pruritus (5%)

Nervous system: Dizziness (5%), pain (8%)

Neuromuscular & skeletal: Arthralgia (8%)

Vaginal insert (percentages reported with assisted reproductive technology):

>10%: Gastrointestinal: Abdominal pain (12%)

1% to 10%:

Cardiovascular: Peripheral edema (<2%)

Dermatologic: Urticaria (<2%)

Gastrointestinal: Abdominal distention (4%), constipation (2% to 3%), nausea (7% to 8%), vomiting (2% to 3%)

Genitourinary: Ovarian hyperstimulation syndrome (7%), urinary tract infection (1% to 2%), uterine spasm (3% to 4%), vaginal discomfort (<2%), vaginal hemorrhage (3%), vulvovaginal burning (<2%), vulvovaginal irritation (<2%), vulvovaginal pruritus (<2%)

Nervous system: Fatigue (2% to 3%), headache (3% to 4%)

Postmarketing (all formulations):

Cardiovascular: Circulatory shock, congenital heart disease, hypertension, hypotension, syncope, tachycardia

Endocrine & metabolic: Heavy menstrual bleeding, increased serum glucose, menstrual disease

Gastrointestinal: Acute pancreatitis, cholestasis, dysphagia

Genitourinary: Abnormal uterine bleeding, endometrial carcinoma, male hypospadias, ovarian cyst, spontaneous abortion

Hepatic: Cholestatic hepatitis, hepatic failure, hepatic necrosis, hepatitis, increased liver enzymes (including increased gamma-glutamyl transferase, increased serum alanine aminotransferase, increased serum aspartate aminotransferase), jaundice

Hypersensitivity: Anaphylaxis, facial edema, hypersensitivity reaction, swollen tongue

Nervous system: Abnormal gait, aggressive behavior, choking sensation, confusion, depersonalization, disorientation, dysarthria, feeling abnormal, impaired consciousness, intoxicated feeling, loss of consciousness, paresthesia, sedated state, seizure, slurred speech, stupor, suicidal ideation, transient ischemic attacks, vertigo

Ophthalmic: Blurred vision, diplopia, visual disturbance

Otic: Tinnitus

Respiratory: Asthma, dyspnea, pharyngeal edema

Contraindications

Oral: Hypersensitivity to progesterone or any component of the formulation, including peanuts/peanut oil; undiagnosed abnormal genital bleeding; breast cancer (known, suspected, or history of); active deep vein thrombosis, pulmonary embolism, or history of these conditions; active or history of arterial thromboembolic disease (eg, stroke, MI); hepatic impairment or disease; pregnancy.

IM: Hypersensitivity to progesterone or any component of the formulation, including sesame oil/seeds; active or history of thrombophlebitis, thromboembolic disorders, or cerebral apoplexy; undiagnosed vaginal bleeding; hepatic impairment or disease; known or suspected malignancy of the breast or genital organs; missed abortion.

Vaginal gel: Hypersensitivity to progesterone or any component of the formulation, including palm oil; undiagnosed vaginal bleeding; hepatic impairment or disease; known or suspected malignancy of the breast or genital organs; missed abortion; active thrombophlebitis or thromboembolic disorders, or a history of hormone-associated thrombophlebitis or thromboembolic disorders.

Vaginal insert: Hypersensitivity to progesterone or any component of the formulation; undiagnosed vaginal bleeding; known missed abortion or ectopic pregnancy; hepatic disease; known or suspected malignancy of the breast or genital organs; active or history of arterial or venous thromboembolism or severe thrombophlebitis.

Canadian labeling: Additional contraindications (not in the US labeling):

Capsules: Hypersensitivity to soya; endometrial hyperplasia; classical migraine; partial or complete loss of vision due to ophthalmic vascular disease.

Intravaginal gel: Known or suspected progesterone dependent malignancy; acute porphyria, cerebral apoplexy.

Vaginal insert/tablet: Porphyria; undiagnosed vaginal bleeding.

Warnings/Precautions

Concerns related to adverse effects:

• Breast cancer: Estrogen with or without progestogen for the management of menopausal symptoms may be associated with an increased risk of breast cancer. The risk of breast cancer in patients who are postmenopausal on hormone therapy may depend upon type of estrogen and/or progestogen, dose, timing of therapy initiation, duration of therapy, route of administration, and individual patient characteristics (AACE/ACE [Cobin 2017]; NAMS 2022). Hormone therapy may be associated with increased breast density (NAMS 2022); an increase in abnormal mammogram findings requiring further evaluation has been reported with estrogen alone or in combination with progestogen therapy.

• CNS depression: Oral progesterone may cause CNS depression, which may impair physical or mental abilities; patients must be cautioned about performing tasks that require mental alertness (eg, operating machinery, driving).

• Dementia: Do not use progestogen plus estrogens for the prevention of dementia. Hormone therapy is not recommended at any age to prevent or treat cognitive decline or dementia (AACE [Goodman 2011]; NAMS 2022).

• Endometrial cancer: Progesterone is used to reduce the risk of endometrial hyperplasia in patients who are postmenopausal with a uterus receiving conjugated estrogens. The use of unopposed estrogen in patients with an intact uterus is associated with an increased risk of endometrial cancer. The addition of a progestogen to estrogen therapy may decrease the risk of endometrial hyperplasia, a precursor to endometrial cancer.

• Endometriosis: Estrogens may exacerbate endometriosis. Malignant transformation of residual endometrial implants has been reported posthysterectomy with unopposed estrogen therapy. Consider adding a progestogen in patients with residual endometriosis posthysterectomy.

• Eosinophilic pneumonia: Cases of acute eosinophilic pneumonia have been reported with use of progesterone injection in sesame oil; symptoms have included fever, dyspnea with hypoxic respiratory insufficiency, and diffuse pulmonary infiltrates and generally develop 2 to 4 weeks after treatment initiation. Discontinue immediately and undergo prompt medical evaluation if symptoms of eosinophilic pneumonia occur.

• Fluid retention: May cause fluid retention; use with caution in patients with diseases which may be exacerbated by fluid retention, including asthma, cardiac or renal impairment, epilepsy, and migraine.

• Ovarian cancer: Available information related to the use of menopausal estrogen or estrogen/progestogen therapy and risk of ovarian cancer is inconsistent. If an association is present, the absolute risk is likely rare and may be influenced by duration of therapy (AACE [Goodman 2011]; ES [Stuenkel 2015]; NAMS 2022).

• Retinal thrombosis: Discontinue pending examination in cases of sudden partial or complete vision loss, sudden onset of proptosis, diplopia, or migraine; discontinue permanently if papilledema or retinal vascular lesions are observed on examination.

• Toxic shock: Toxic shock syndrome (TSS) has been reported in patients using vaginal systems with and without tampon use; discontinue use if TSS is suspected and initiate appropriate treatment.

Disease-related concerns:

• Cardiovascular disease: Do not use progestogen plus estrogen for the prevention of cardiovascular disease. In the Women's Health Initiative studies, an increased risk of deep vein thrombosis, pulmonary embolism, stroke, and myocardial infarction was observed in patients taking conjugated estrogens combined with medroxyprogesterone. Additional risk factors include diabetes mellitus, hypercholesterolemia, hypertension, systemic lupus erythematosus, obesity, tobacco use, and/or history of venous thromboembolism (VTE). Manage risk factors appropriately; discontinue immediately if adverse cardiovascular events occur or are suspected.

• Diabetes: May impair glucose tolerance; use caution in patients with diabetes. Prior to therapy, consider age, cardiovascular and metabolic risk factors in patients previously diagnosed with diabetes (AACE/ACE [Cobin 2017]).

Special populations:

• Surgery: Whenever possible, discontinue progestogens in combination with estrogens at least 4 to 6 weeks prior to elective surgery associated with an increased risk of thromboembolism or during periods of prolonged immobilization.

Dosage form specific issues:

• Benzyl alcohol and derivatives: Some dosage forms may contain benzyl alcohol; large amounts of benzyl alcohol (≥99 mg/kg/day) have been associated with a potentially fatal toxicity ("gasping syndrome") in neonates; the "gasping syndrome" consists of metabolic acidosis, respiratory distress, gasping respirations, CNS dysfunction (including convulsions, intracranial hemorrhage), hypotension, and cardiovascular collapse (AAP ["Inactive" 1997]; CDC 1982); some data suggests that benzoate displaces bilirubin from protein binding sites (Ahlfors 2001); avoid or use dosage forms containing benzyl alcohol with caution in neonates. See manufacturer's labeling.

• Palm oil: Some products may contain palm oil.

• Peanut oil: Some products may contain peanut oil.

• Sesame oil: Some products may contain sesame oil.

Other warnings/precautions:

• Risks vs benefits: When used for the relief of menopausal symptoms, the benefit-risk of hormone therapy is most favorable if started in patients who have no contraindications to therapy, are <60 years of age, within 10 years of menopause onset, have a favorable lipid profile, and do not have the factor V Leiden genotype or metabolic syndrome. Consider cardiovascular disease risk factors when evaluating therapy and route of administration (AACE/ACE [Cobin 2017]; NAMS 2022). Use at the lowest effective doses and for the shortest duration consistent with treatment goals and risks for the individual patient. Reevaluate patients as clinically appropriate to determine if treatment is still necessary. Available data related to treatment risks are from WHI studies, which evaluated oral conjugated estrogens with medroxyprogesterone relative to placebo in patients who are postmenopausal. Other combinations and dosage forms of estrogens and progestogens were not studied; assume outcomes to be similar for other doses and other dosage forms of estrogens and progestogens until comparable data becomes available.

Dosage Forms Considerations

Progesterone cream 10% and vaginal suppositories are compounding kits. Refer to manufacturer’s labeling for compounding instructions.

Dosage Forms: US

Excipient information presented when available (limited, particularly for generics); consult specific product labeling.

Capsule, Oral:

Prometrium: 100 mg [contains fd&c red #40 (allura red ac dye), peanut oil, quinoline yellow (d&c yellow #10)]

Prometrium: 200 mg [contains fd&c yellow #6 (sunset yellow), peanut oil, quinoline yellow (d&c yellow #10)]

Generic: 100 mg, 200 mg

Gel, Vaginal:

Crinone: 4% (1.125 g); 8% (1.125 g)

Insert, Vaginal:

Endometrin: 100 mg (1 ea, 21 ea)

Oil, Intramuscular:

Generic: 50 mg/mL (10 mL)

Generic Equivalent Available: US

May be product dependent

Pricing: US

Capsules (Progesterone Oral)

100 mg (per each): $2.05 - $5.17

200 mg (per each): $3.89 - $9.82

Capsules (Prometrium Oral)

100 mg (per each): $20.01

200 mg (per each): $38.01

Gel (Crinone Vaginal)

4% (per gram): $19.11

8% (per gram): $31.88

INST (Endometrin Vaginal)

100 mg (per each): $17.02

Oil (Progesterone Intramuscular)

50 mg/mL (per mL): $2.40 - $5.01

Disclaimer: A representative AWP (Average Wholesale Price) price or price range is provided as reference price only. A range is provided when more than one manufacturer's AWP price is available and uses the low and high price reported by the manufacturers to determine the range. The pricing data should be used for benchmarking purposes only, and as such should not be used alone to set or adjudicate any prices for reimbursement or purchasing functions or considered to be an exact price for a single product and/or manufacturer. Medi-Span expressly disclaims all warranties of any kind or nature, whether express or implied, and assumes no liability with respect to accuracy of price or price range data published in its solutions. In no event shall Medi-Span be liable for special, indirect, incidental, or consequential damages arising from use of price or price range data. Pricing data is updated monthly.

Dosage Forms: Canada

Excipient information presented when available (limited, particularly for generics); consult specific product labeling.

Capsule, Oral:

Prometrium: 100 mg [contains soybean lecithin]

Generic: 100 mg, 200 mg

Gel, Vaginal:

Crinone: 8% (1.45 g)

Insert, Vaginal:

Endometrin: 100 mg (21 ea)

Oil, Intramuscular:

Generic: 50 mg/mL (10 mL)

Administration: Adult

IM: May cause injection-site irritation.

Intravaginal:

Vaginal gel: A small amount of gel will remain in the applicator following insertion. Administer into the vagina directly from sealed applicator. Remove applicator from wrapper; holding applicator on each side, push plunger into applicator until it snaps into place; twist off cap counterclockwise; gently insert into vagina and push plunger. Do not use concomitantly with other local vaginal therapy. If concomitant therapy cannot be avoided, administer other vaginal products at least 6 hours before or 6 hours after progesterone administration. Small white globules may appear as vaginal discharge. If a dose increase from 4% to 8% is needed for the treatment of secondary amenorrhea, the 8% gel must be used. Increasing the volume of the 4% gel does not increase the amount of progesterone absorbed.

Vaginal insert: Insert tablet in vagina using disposable applicator provided. Concomitant use with other vaginal products (eg, antifungals) has not been studied; release and absorption from the insert may be altered.

Capsule (off-label route): When the oral capsule is used for spontaneous preterm birth prevention, doses are administered intravaginally at bedtime (Ref).

Oral: Administer at bedtime. For patients who experience difficulty swallowing the capsules, taking with a full glass of water in the standing position may be beneficial.

Hazardous Drugs Handling Considerations

Hazardous agent (NIOSH 2016 [group 2]).

Use appropriate precautions for receiving, handling, storage, preparation, dispensing, transporting, administration, and disposal. Follow NIOSH and USP 800 recommendations and institution-specific policies/procedures for appropriate containment strategy (NIOSH 2016; USP-NF 2020).

Note: Facilities may perform risk assessment of some hazardous drugs to determine if appropriate for alternative handling and containment strategies (USP-NF 2020). Refer to institution-specific handling policies/procedures.

Use: Labeled Indications

Assisted reproductive technology: Progesterone replacement or supplementation as part of assisted reproductive technology (ART) for infertile patients with progesterone deficiency (Crinone vaginal gel). To support embryo implantation and early pregnancy by supplementation of corpus luteal function as part of ART (Endometrin vaginal insert).

Limitations of use: Products are indicated for infertile patients to support or maintain a clinical pregnancy. Efficacy of vaginal insert in patients ≥35 years of age has not been established.

Estrogen therapy-associated endometrial hyperplasia, prevention: Prevention of endometrial hyperplasia in patients with a uterus receiving estrogen therapy (eg, for vasomotor symptoms associated with menopause or secondary amenorrhea).

Secondary amenorrhea, diagnostic aid ("progesterone challenge"): For use as a diagnostic aid to determine endometrial estrogen exposure and/or uterine or outflow tract abnormality.

Uterine bleeding, abnormal: Treatment of abnormal uterine bleeding due to hormonal imbalance in the absence of organic pathology, such as submucous fibroids or uterine cancer (IM injection).

Use: Off-Label: Adult

Spontaneous preterm birth, prevention

Medication Safety Issues
High alert medication:

The Institute for Safe Medication Practices (ISMP) includes this medication among its list of drugs (contraindicated in pregnancy) which have a heightened risk of causing significant patient harm when used in error (High-Alert Medications in Community/Ambulatory Care Settings).

Metabolism/Transport Effects

Substrate of CYP1A2 (minor), CYP2A6 (minor), CYP2C19 (minor), CYP2C9 (minor), CYP2D6 (minor), CYP3A4 (minor); Note: Assignment of Major/Minor substrate status based on clinically relevant drug interaction potential

Drug Interactions

Note: Interacting drugs may not be individually listed below if they are part of a group interaction (eg, individual drugs within “CYP3A4 Inducers [Strong]” are NOT listed). For a complete list of drug interactions by individual drug name and detailed management recommendations, use the drug interactions program by clicking on the “Launch drug interactions program” link above.

Antidiabetic Agents: Hyperglycemia-Associated Agents may diminish the therapeutic effect of Antidiabetic Agents. Risk C: Monitor therapy

Antifungal Agents (Vaginal): May diminish the therapeutic effect of Progesterone. Risk X: Avoid combination

Chlorprothixene: Progestins may enhance the adverse/toxic effect of Chlorprothixene. Progestins may enhance the therapeutic effect of Chlorprothixene. Risk C: Monitor therapy

MetyraPONE: Progestins may diminish the diagnostic effect of MetyraPONE. Management: Consider alternatives to the use of the metyrapone test in patients taking progestins. Risk D: Consider therapy modification

Sincalide: Drugs that Affect Gallbladder Function may diminish the therapeutic effect of Sincalide. Management: Consider discontinuing drugs that may affect gallbladder motility prior to the use of sincalide to stimulate gallbladder contraction. Risk D: Consider therapy modification

Ulipristal: May diminish the therapeutic effect of Progestins. Progestins may diminish the therapeutic effect of Ulipristal. Risk X: Avoid combination

Food Interactions

Capsule: Food increases oral bioavailability.

Reproductive Considerations

Progesterone is indicated for use in assisted reproductive technology to support embryo implantation. In addition, some products are used for the treatment of amenorrhea; spontaneous menstrual cycles are expected following therapy.

In transgender patients undergoing masculinizing hormone therapy, progesterone has been used as an alternative to hysterectomy or endometrial ablation to induce amenorrhea when testosterone therapy does not suppress menstruation (ACOG 2021b; Ahmad 2017).

Pregnancy Considerations

Adverse events following oral maternal use in pregnancy (eg, hypospadias, congenital heart disease, cleft lip/palate) have been noted in postmarketing data; however, a causal relationship has not been clearly established. Adequate progesterone concentrations are required for embryo implantation and maintenance of pregnancy. Based on available data, increased risks of birth defects or adverse neurodevelopment have not been observed following maternal use for the prevention of preterm birth or when used as indicated as part of assisted reproductive technology (ART) (Coomarasamy 2020; Cuijpers 2021; Czyzyk 2017; Simons 2021).

Progesterone is used to maintain pregnancy as part of ART.

Intravaginal progesterone is recommended to reduce the risk of spontaneous preterm birth in patients with a singleton pregnancy, no prior preterm birth, and a cervical length <25 mm. Intravaginal progesterone may also be offered to patients with a singleton pregnancy, prior preterm birth, and a cervical length <25 mm. Although the exact timing and schedule for treatment is not well defined, use is generally started after diagnosis following scheduled transvaginal ultrasound. Patients with no prior preterm birth generally undergo cervical ultrasound between 18 and 22 weeks' gestation; patients with prior spontaneous preterm birth generally undergo serial cervical ultrasounds between 16 and 24 weeks' gestation (ACOG 2021a; EPPPIC Group 2021; Romero 2018). Although not available as an FDA-approved dosage form in the United States, some studies used the vaginal gel off-label for this indication; others used oral capsules intravaginally (off-label route and indication) or compounded vaginal suppositories (Romero 2018). Orally administered progesterone has also been evaluated to reduce the risk of spontaneous preterm birth. However, additional data are needed to make recommendations (Boelig 2019; Care 2022; EPPPIC Group 2021). Data are insufficient to recommend routine use in patients with multiple gestations (ACOG 2021a; EPPPIC Group 2021; Romero 2018).

Progesterone has been studied in patients with a history of miscarriage. Current evidence is conflicting regarding whether progesterone increases live birth rates in patients with threatened or recurrent miscarriages; use may be beneficial for patients with previous miscarriages and early pregnancy bleeding or with a high number of previous miscarriages (Coomarasamy 2021a; Coomarasamy 2021b; Devall 2021).

Breastfeeding Considerations

Progesterone is present in breast milk.

In transgender patients undergoing feminizing hormone therapy, case reports describe the use of progesterone (in combination with other therapies) to induce lactation in patients who wish to breastfeed (Reisman 2018; Wamboldt 2021).

Breastfeeding recommendations vary by manufacturer; the decision to breastfeed during therapy should consider the risk of infant exposure, the benefits of breastfeeding to the infant, and the benefits of treatment to the mother.

Monitoring Parameters

Vaginal bleeding.

Assisted reproductive technology: Consider monitoring serum progesterone, particularly with intravaginal administration (Labarta 2020).

Menopause: Prior to combination hormonal therapy, baseline risk for breast cancer and CVD. During therapy, age appropriate breast and pelvic exams; blood pressure; unscheduled bleeding lasting >6 months for endometrial pathology (sooner in patients who are obese, diabetic, or have a history of endometrial cancer); serum triglycerides (2 weeks after starting therapy in patients with baseline level >200 mg/dL); TSH (6 to 12 weeks after starting oral therapy in patients taking thyroid replacement); efficacy beginning 1 to 3 months after starting therapy, then every 6 to 12 months as appropriate. Duration of treatment should be evaluated at least annually (ES [Stuenkel 2015]).

Mechanism of Action

Natural steroid hormone that induces secretory changes in the endometrium, promotes mammary gland development, relaxes uterine smooth muscle, blocks follicular maturation and ovulation, and maintains pregnancy. When used as part of an ART program in the luteal phase, progesterone supports embryo implantation.

Pharmacokinetics (Adult Data Unless Noted)

Absorption: Vaginal gel: Prolonged.

Absorption half-life: Vaginal gel: ~25 to 50 hours.

Protein binding: ~96% to 99%, primarily to albumin (50% to 54%) and cortisol-binding protein (43% to 48%).

Metabolism: Hepatic to pregnanediols and pregnanolones, which are then conjugated to glucuronide and sulfate metabolites; metabolites excreted in the bile may be deconjugated and further metabolized in the intestine via reduction, dehydroxylation, and epimerization.

Half-life elimination: Vaginal gel: 5 to 20 minutes.

Time to peak: Oral: Within 3 hours; IM: ~8 hours; Intravaginal gel: 3.55 ± 2.48 hours to 7 ± 2.88 hours; Vaginal insert: 17.3 to 24 hours.

Excretion: Urine (50% to 60% as metabolites); bile, feces (~10%).

Brand Names: International
International Brand Names by Country
For country code abbreviations (show table)

  • (AE) United Arab Emirates: Crinone | Cyclogest | Progesta | Proluton | Utrogestan;
  • (AR) Argentina: Crinone | Faselut | Geslutin | Gester | Gestfem | Mafel | Progest | Progesterona Asofarma | Proluton | Utrogestan;
  • (AT) Austria: Arefam | Cyclogest | Utrogestan;
  • (AU) Australia: Crinone | Cyclogest | Proluton | Prometrium | Utrogestan;
  • (BD) Bangladesh: Microgest | Progel;
  • (BE) Belgium: Amelgen | Crinone | Progestogel | Utrogestan;
  • (BF) Burkina Faso: Progestogel | Utrogestan;
  • (BG) Bulgaria: Crinone | Cyclogest | Luteinum | Progesteron | Progestogel | Utrogestan;
  • (BR) Brazil: Agape | Crinone | Evocanil | Gynpro | Junno | Progesterona | Utrogestan;
  • (CH) Switzerland: Progestogel | Utrogestan;
  • (CI) Côte d'Ivoire: Aprogest | Prostium;
  • (CL) Chile: Crinone | Endometrin | Gestel | Hormoral | Progendo | Progesterona | Progeva;
  • (CN) China: Qi ning | Utrogestan | Yi ma xin;
  • (CO) Colombia: Crinone | Cyclogest | Geslutin | Geslutin pnm | Gesprogen | Gestacent | Gestageno | Jarit | Progeffik | Progendo | Progesterona | Progestogel | Utrogestan;
  • (CZ) Czech Republic: Agolutin | Amelgen | Crinone | Gynprodyl | Progesteron besins | Utrogestan;
  • (DE) Germany: Crinone | Cyclogest | Estima | Famenita | Progebel | Progestan | Progesteron kade/besins | Progesteron yes | Progestogel | Utrogest | Utrogest luteal | Utrogestan;
  • (DO) Dominican Republic: Crinone | Etiprogest | Geslutin | Gestageno | Jarit | Progeffik | Progest | Progesterona | Progesterona-Alfa | Sugest | Utrogestan;
  • (EC) Ecuador: Crinone | Cuerpo amarillo fuerte | Geslutin | Geslutin pnm | Gestageno | Hormoral | Jarit | Microgest | Misocheck | Progeffik | Progendo | Progest | Progestin | Progestogel | Utrogestan;
  • (EE) Estonia: Amelgen | Crinone | Gepretix | Lugesteron | Utrogestan;
  • (EG) Egypt: Crinone | Cyclogest | Cyclotrone | Hystrogest | Lutone | Progesing | Progest | Prontogest | Utrocare | Utrogestan;
  • (ES) Spain: Crinone | Cyclogest | Darstin | Progeffik | Utrogestan;
  • (ET) Ethiopia: Progesta;
  • (FI) Finland: Crinone | Cyclogest | Lugesteron;
  • (FR) France: Crinone | Estima | Evapause | Menaelle | Progestan | Progesterone Biogaran | Progesterone gnr | Progesterone merck | Progesterone Ratiopharm | Progesterone teva | Progestogel | Utrogestan;
  • (GB) United Kingdom: Crinone | Cyclogest cox | Gepretix | Gestone | Utrogestan | Utrogestan Vaginal;
  • (GR) Greece: Crinone | Cyclogest | Gestone | Gynalven | Proluton | Titho | Utrogestan | Vasclor;
  • (HK) Hong Kong: Crinone | Progestogel | Utrogestan;
  • (HR) Croatia: Cyclogest | Utrogestan;
  • (HU) Hungary: Crinone | Cyclogest | Glanducorpin | Progesterone exeltis | Utrogestan;
  • (ID) Indonesia: Cygest | Gynprogest | Utrogestan;
  • (IE) Ireland: Crinone | Gestone | Utrogestan;
  • (IL) Israel: Crinone | Gestone | Utrogestan;
  • (IN) India: Algest | Alpreg sofsule | Aprogest | Aqsusten | Artgest | Aurich | Axitron | C hop | Celogest | Conest | Corion-np | Crinone | Cygest | Dubagest | E gest | Egeria | Emprogest | Endogest | Etgel | Ets | Eugest | Evateron | Fegest | Freegest | Fulgest | Gestafine | Gestasure | Gesterol | Gestmate | Gestoc | Gestofit | Gestone | Gestorin | Gestovel | Gynarone | Hald | Her nmp | Hilgestrone | Hope | Hormorin | Ibigest | Leutipreg | Loeva | Lps | Lupigest | Luteum | Macgest | Megagest | Michelle | Microgest | Microprogesta | Minagest | Miprogen | Myprog | N gest | Naeva | Nance | Natron | Naturogest | Neogest | Nidagen | Nt-natal mp | Nugest | Ogest | Orgagest | Posito ts | Pregafem | Pregcert | Pregcitil | Pregtain | Prenone | Pro-one | Profine | Progestal | Progminat | Prolin | Puregest | Remens | Retain | Ronygest | Seacure | Sofia | Sperogest | Srgest | Strone | Sugest | Susten | Ulitgest | Ultigest | Uniprogestin | Uterone | Utreva | Utrogestan | Utrovin | Vageston | Voranin | Walagest | Wisrone | Zesty;
  • (IT) Italy: Amelgen | Crinone | Esolut | Lutogin | Progeffik | Progestogel | Prometrium | Prontogest;
  • (JO) Jordan: Biogest | Crinone | Cyclogest | Gestophil | Progesta | Utrogestran;
  • (JP) Japan: Dep progen | F meno | Luteum | Onecrinone | Proge hormon | Progesteron showa | Progesterone abbott | Progeston | Proluton | Utrogestan;
  • (KE) Kenya: Bergestron | Crinone | Prontogest | Prostar | Prostium | Susten | Utrogestan | Utrogestan Vaginal | Zesbina;
  • (KR) Korea, Republic of: Crinone | Cyclogest | Estima | Progest | Progesteron | Progesto | Sugest | Utrogestan | Yenatron;
  • (KW) Kuwait: Cyclogest;
  • (LB) Lebanon: Biogest | Crinone | Cyclogest | Darstin | Progest | Progestogel | Proluton | Prontogest | Utrogestan;
  • (LT) Lithuania: Agolutin | Crinone | Cyclogest | Gepretix | Progesteron | Progestogel | Utrogest | Utrogestan;
  • (LU) Luxembourg: Amelgen | Crinone | Progebel | Progestogel | Utrogestan;
  • (LV) Latvia: Agolutin | Amelgen | Crinone | Gepretix | Lugesteron | Progesteron | Progesterone besins | Progestogel | Utrogest | Utrogestan;
  • (MA) Morocco: Gestel | Progestogel | Projeva | Uteron | Utrogestan;
  • (MX) Mexico: Burlen | Crinone | Docupren | Gepromi | Geslutin | Gestageno | Mefiros | Premastan | Progesterona | Prolidon | Utrogestan;
  • (MY) Malaysia: Crinone | Progestogel | Utrogestan;
  • (NG) Nigeria: Unoprog;
  • (NL) Netherlands: Crinone | Cyclogest | Progestan | Progestine | Utrogestan;
  • (NO) Norway: Crinone | Cyclogest | Prontogest | Utrogest | Utrogestan;
  • (NZ) New Zealand: Crinone | Gestone | Utrogestan;
  • (PE) Peru: Ciclosterona fuerte | Crinone | Geslutin | Geslutin pnm | Gestageno | Hormoral | Jarit | Misocheck | Misulona | Progendo | Progestogel | Progeva | Utrogestan;
  • (PH) Philippines: Crinone | Gestron | Heragest | Utrogestan;
  • (PK) Pakistan: Cyclogest | Progeffik | Progesteron | Progestin | U progest | Utrogestan;
  • (PL) Poland: Agolutin | Crinone | Cyclogest | Luttagen | Progesterone besins | Progesterone goodlife fertility | Progesteronum | Progestogel | Utrogestan;
  • (PR) Puerto Rico: Crinone | Gesterol | Prochieve | Progesterone in oil | Prometrium;
  • (PT) Portugal: Crinone | Cyclogest | Progeffik | Progenar | Progestogel | Utrogestan;
  • (PY) Paraguay: Femproges | Gynprogest | Mafel | Progeffik | Progendo;
  • (QA) Qatar: Crinone | Cyclogest | Endometrin | Gestophil | Progesta | Progestan | Prolutex | Utrogestan | Utrogestan (Oral/Vaginal);
  • (RO) Romania: Arefam | Crinone | Mastoprofen | Progestogel | Utrogestan;
  • (RU) Russian Federation: Crinone | Dlyjens pro | Iprozhin | Pragisan | Prajisun | Progesteron | Progestogel | Utrogestan | Vanel;
  • (SA) Saudi Arabia: Crinone | Cyclogest | Gestone | Progesteron;
  • (SE) Sweden: Crinone | Cyclogest | Utrogestan;
  • (SG) Singapore: Crinone | Progestogel | Utrogestan;
  • (SI) Slovenia: Amelgen | Crinone | Estima ge | Progestogel | Utrogestan;
  • (SK) Slovakia: Agolutin | Amelgen | Crinone | Progesterone ladeepharma | Utrogestan;
  • (TH) Thailand: Crinone | Cyclogest | Prodion | Progestogel | Utrogestan;
  • (TN) Tunisia: Cyclogest | Estima | Progest | Progesterone mylan | Progestogel | Utrogestan;
  • (TR) Turkey: Crinone | Cyclogest | Progestan | Progynex | Promester;
  • (TW) Taiwan: Crinone | Progeffik | Progesteron | Progeston | Promone | Utrogestan;
  • (UA) Ukraine: Crinone | Progesteron | Progestogel | Proginorm gesta | Proginorm ovo | Utrogestan;
  • (UG) Uganda: Crinone | Prostar | Unoprog;
  • (UY) Uruguay: Crinone | Cyclogest | Geslutin pnm | Progelle | Progestan | Progestogel | Utrogestan;
  • (VE) Venezuela, Bolivarian Republic of: Crinone | Cyclogest | Geslutin | Jarit | Progendo | Progestogel | Utrogestan;
  • (VN) Viet Nam: Miprotone | Progentin;
  • (ZA) South Africa: Cyclogest | Utrogestan;
  • (ZM) Zambia: Hormorin;
  • (ZW) Zimbabwe: Utrogestan
  1. <800> Hazardous Drugs—Handling in Healthcare Settings. United States Pharmacopeia and National Formulary (USP 43-NF 38). Rockville, MD: United States Pharmacopeia Convention; 2020:74-92.
  2. Ackerman KE, Singhal V, Baskaran C, et al. Oestrogen replacement improves bone mineral density in oligo-amenorrhoeic athletes: a randomised clinical trial. Br J Sports Med. 2019;53(4):229-236. doi:10.1136/bjsports-2018-099723 [PubMed 30301734]
  3. Ackerman KE, Singhal V, Slattery M, et al. Effects of estrogen replacement on bone geometry and microarchitecture in adolescent and young adult oligoamenorrheic athletes: a randomized trial. J Bone Miner Res. 2020;35(2):248-260. doi:10.1002/jbmr.3887 [PubMed 31603998]
  4. Ahlfors CE. Benzyl alcohol, kernicterus, and unbound bilirubin. J Pediatr. 2001;139(2):317-319. [PubMed 11487763]
  5. Ahmad S, Leinung M. The response of the menstrual cycle to initiation of hormonal therapy in transgender men. Transgend Health. 2017;2(1):176-179. doi:10.1089/trgh.2017.0023 [PubMed 29159311]
  6. American College of Obstetricians and Gynecologists' Committee on Practice Bulletins—Obstetrics. Prediction and prevention of spontaneous preterm birth: ACOG practice bulletin, number 234. Obstet Gynecol. 2021a;138(2):e65-e90. doi:10.1097/AOG.0000000000004479 [PubMed 34293771]
  7. American College of Obstetricians and Gynecologists. Committee opinion no. 698: hormone therapy in primary ovarian insufficiency. Obstet Gynecol. 2017;129(5):e134-e141. doi:10.1097/AOG.0000000000002044 [PubMed 28426619]
  8. American College of Obstetricians and Gynecologists’ Committee on Gynecologic Practice; American College of Obstetricians and Gynecologists’ Committee on Health Care for Underserved Women. Health care for transgender and gender diverse individuals: ACOG committee opinion, number 823. Obstet Gynecol. 2021b;137(3):e75-e88. doi:10.1097/AOG.0000000000004294 [PubMed 33595253]
  9. Anderson GL, Limacher M, Assaf AR, et al, "Effects of Conjugated Equine Estrogen In Postmenopausal Women With Hysterectomy: The Women's Health Initiative Randomized Controlled Trial." JAMA, 2004, 291(14):1701-12. [PubMed 15082697]
  10. Boelig RC, Della Corte L, Ashoush S, et al. Oral progesterone for the prevention of recurrent preterm birth: systematic review and metaanalysis. Am J Obstet Gynecol MFM. 2019;1(1):50-62. doi:10.1016/j.ajogmf.2019.03.001 [PubMed 31172132]
  11. Bosch E, Broer S, Griesinger G, et al; the Eshre Guideline Group on Ovarian Stimulation. ESHRE guideline: ovarian stimulation for IVF/ICSI. Hum Reprod Open. 2020;2020(2):hoaa009. doi:10.1093/hropen/hoaa009 [PubMed 32395637]
  12. Care A, Nevitt SJ, Medley N, et al. Interventions to prevent spontaneous preterm birth in women with singleton pregnancy who are at high risk: systematic review and network meta-analysis. BMJ. 2022;376:e064547. doi:10.1136/bmj-2021-064547 [PubMed 35168930]
  13. Centers for Disease Control (CDC). Neonatal deaths associated with use of benzyl alcohol—United States. MMWR Morb Mortal Wkly Rep. 1982;31(22):290-291. http://www.cdc.gov/mmwr/preview/mmwrhtml/00001109.htm [PubMed 6810084]
  14. Cetingoz E, Cam C, Sakalh M, et al. Progesterone effects on preterm birth in high-risk pregnancies: a randomized placebo-controlled trial. Arch Gynecol Obstet. 2011283(3):423-429. [PubMed 20091317]
  15. Cobin RH, Goodman NF; AACE Reproductive Endocrinology Scientific Committee. American Association of Clinical Endocrinologists (AACE) and American College of Endocrinology (ACE) position statement on menopause-2017 update. Endocr Pract. 2017;23(7):869-880. doi: 10.4158/EP171828.PS. [PubMed 28703650]
  16. Coomarasamy A, Devall AJ, Brosens JJ, et al. Micronized vaginal progesterone to prevent miscarriage: a critical evaluation of randomized evidence. Am J Obstet Gynecol. 2020;223(2):167-176. doi:10.1016/j.ajog.2019.12.006 [PubMed 32008730]
  17. Coomarasamy A, Dhillon-Smith RK, Papadopoulou A, et al. Recurrent miscarriage: evidence to accelerate action. Lancet. 2021a;397(10285):1675-1682. doi:10.1016/S0140-6736(21)00681-4 [PubMed 33915096]
  18. Coomarasamy A, Gallos ID, Papadopoulou A, et al. Sporadic miscarriage: evidence to provide effective care. Lancet. 2021b;397(10285):1668-1674. doi:10.1016/S0140-6736(21)00683-8 [PubMed 33915095]
  19. Crinone (progesterone) [prescribing information]. Parsippany, NJ: Actavis Pharma; June 2017.
  20. Crinone (progesterone) [product monograph]. Mississauga, Ontario, Canada: EMD Inc Canada; July 2023.
  21. Cuijpers CJJ, Van't Hooft J, Schneeberger C, et al. Progesterone for prevention of preterm birth in women with short cervical length: 2-year infant outcomes. Ultrasound Obstet Gynecol. 2021;57(3):431-439. doi:10.1002/uog.23126 [PubMed 32959909]
  22. Czyzyk A, Podfigurna A, Genazzani AR, Meczekalski B. The role of progesterone therapy in early pregnancy: from physiological role to therapeutic utility. Gynecol Endocrinol. 2017;33(6):421-424. doi:10.1080/09513590.2017.1291615 [PubMed 28277122]
  23. De Souza MJ, Nattiv A, Joy E, et al; Expert Panel. 2014 Female Athlete Triad Coalition consensus statement on treatment and return to play of the female athlete triad: 1st international conference held in San Francisco, California, May 2012 and 2nd international conference held in Indianapolis, Indiana, May 2013. Br J Sports Med. 2014;48(4):289. doi:10.1136/bjsports-2013-093218 [PubMed 24463911]
  24. Devall AJ, Papadopoulou A, Podesek M, et al. Progestogens for preventing miscarriage: a network meta-analysis. Cochrane Database Syst Rev. 2021;4:CD013792. doi:10.1002/14651858.CD013792.pub2 [PubMed 33872382]
  25. Devine K, Richter KS, Jahandideh S, Widra EA, McKeeby JL. Intramuscular progesterone optimizes live birth from programmed frozen embryo transfer: a randomized clinical trial. Fertil Steril. 2021;116(3):633-643. doi:10.1016/j.fertnstert.2021.04.013 [PubMed 33992421]
  26. Doody KJ1, Schnell VL, Foulk RA, et al. Endometrin for luteal phase support in a randomized, controlled, open-label, prospective in-vitro fertilization trial using a combination of Menopur and Bravelle for controlled ovarian hyperstimulation. Fertil Steril. 2009;91(4):1012-1017. [PubMed 18371963]
  27. Endometrin (progesterone) [prescribing information]. Parsippany, NJ: Ferring Pharmaceuticals Inc; January 2018.
  28. Endometrin (progesterone) [product monograph]. North York, Ontario, Canada: Ferring Inc; May 2015.
  29. EPPPIC Group. Evaluating Progestogens for Preventing Preterm birth International Collaborative (EPPPIC): meta-analysis of individual participant data from randomised controlled trials. Lancet. 2021;397(10280):1183-1194. doi:10.1016/S0140-6736(21)00217-8 [PubMed 33773630]
  30. Fonseca EB, Celik E, Parra M, Singh M, and Nicolaides KH. Progesterone and the risk of preterm birth among women with a short cervix. N Engl J Med. 2007;375(5):462-469. [PubMed 17671254]
  31. Goodman NF, Cobin RH, Ginzburg SB, et al; American Association of Clinical Endocrinologists (AACE). American Association of Clinical Endocrinologists Medical Guidelines for Clinical Practice for the diagnosis and treatment of menopause. Endocr Pract. 2011;17(suppl 6):1-25. doi:10.4158/ep.17.s6.1 [PubMed 22193047]
  32. Gordon CM, Ackerman KE, Berga SL, et al. Functional hypothalamic amenorrhea: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab. 2017;102(5):1413-1439. doi: 10.1210/jc.2017-00131 [PubMed 28368518]
  33. Hassan SS, Romero R, Vidyadhari D, et al; PREGNANT trial. Vaginal progesterone reduces the rate of preterm birth in women with a sonographic short cervix: a multicenter, randomized, double-blind, placebo-controlled trial. Ultrasound Obstet Gynecol. 2011;38(1):18-31. doi:10.1002/uog.9017 [PubMed 21472815]
  34. Hsia J, Langer RD, Manson JE, et al, "Conjugated Equine Estrogens and Coronary Heart Disease: The Women's Health Initiative," Arch Intern Med, 2006, 166(3):357-65. [PubMed 16476878]
  35. "Inactive" ingredients in pharmaceutical products: update (subject review). American Academy of Pediatrics (AAP) Committee on Drugs. Pediatrics. 1997;99(2):268-278. [PubMed 9024461]
  36. Jain V, McDonald SD, Mundle WR, Farine D. Guideline no. 398: progesterone for prevention of spontaneous preterm birth. J Obstet Gynaecol Can. 2020;42(6):806-812. doi:10.1016/j.jogc.2019.04.012 [PubMed 32473687]
  37. Jewson M, Purohit P, Lumsden MA. Progesterone and abnormal uterine bleeding/menstrual disorders. Best Pract Res Clin Obstet Gynaecol. 2020;69:62-73. doi:10.1016/j.bpobgyn.2020.05.004 [PubMed 32698992]
  38. Kuon RJ, Voß P, Rath W. Progesterone for the prevention of preterm birth - an update of evidence-based indications. Geburtshilfe Frauenheilkd. 2019;79(8):844-853. doi:10.1055/a-0854-6472 [PubMed 31423019]
  39. Labarta E, Rodríguez C. Progesterone use in assisted reproductive technology. Best Pract Res Clin Obstet Gynaecol. 2020;69:74-84. doi:10.1016/j.bpobgyn.2020.05.005 [PubMed 32616441]
  40. Majhi P, Bagga R, Kalra J, Sharma M. Intravaginal use of natural micronised progesterone to prevent pre-term birth: a randomised trial in India. J Obstet Gynaecol. 2009;29(6):493-498. doi:10.1080/01443610902980878 [PubMed 19697195]
  41. Martin KA, Barbieri RL. Treatment of menopausal symptoms with hormone therapy. Post TW, ed. UpToDate. Waltham, MA: UpToDate Inc. http://www.uptodate.com. Accessed November 2, 2022.
  42. Meis PJ, Klebanoff M, Thom E, et al; National Institute of Child Health and Human Development Maternal-Fetal Medicine Units Network. Prevention of recurrent preterm delivery by 17 alpha-hydroxyprogesterone caproate [published correction appears in N Engl J Med. 2003;349(13):1299]. N Engl J Med. 2003;348(24):2379-2385. [PubMed 12802023]
  43. Mu E, Kulkarni J. Hormonal contraception and mood disorders. Aust Prescr. 2022;45(3):75-79. doi:10.18773/austprescr.2022.025. Epub 2022 Jun 1. Erratum in: Aust Prescr. 2022;45(4):147. [PubMed 35755988]
  44. Nelson LM. Clinical practice. Primary ovarian insufficiency. N Engl J Med. 2009;360(6):606-614. doi:10.1056/NEJMcp0808697 [PubMed 19196677]
  45. Ng EH, Chan CC, Tang OS, et al, “A Randomized Comparison of Side Effects and Patient Convenience Between Cyclogest® Suppositories and Endometrin® Tablets Used for Luteal Phase Support in IVF Treatment,” Eur J Obstet Gynecol Reprod Biol, 2007, 131(2):182-8. [PubMed 16920249]
  46. Norman JE, Marlow N, Messow CM, et al; OPPTIMUM study group. Vaginal progesterone prophylaxis for preterm birth (the OPPTIMUM study): a multicentre, randomised, double-blind trial. Lancet. 2016;387(10033):2106-2116. doi:10.1016/S0140-6736(16)00350-0 [PubMed 26921136]
  47. North American Menopause Society (NAMS). The 2022 Hormone Therapy Position Statement of the North American Menopause Society Advisory Panel. The 2022 hormone therapy position statement of the North American Menopause Society. Menopause. 2022;29(7):767-794. doi:10.1097/GME.0000000000002028 [PubMed 35797481]
  48. O'Brien JM, Defranco EA, Adair CD, et al; Progesterone Vaginal Gel Study Group. Effect of progesterone on cervical shortening in women at risk for preterm birth: secondary analysis from a multinational, randomized, double-blind, placebo-controlled trial. Ultrasound Obstet Gynecol. 2009;34(6):653-659. doi:10.1002/uog.7338 [PubMed 19918965]
  49. Pabuçcu E, Pabuçcu R, Gürgan T, Tavmergen E. Luteal phase support in fresh and frozen embryo transfer cycles. J Gynecol Obstet Hum Reprod. 2020:101838. doi:10.1016/j.jogoh.2020.101838 [PubMed 32585391]
  50. Popat VB, Calis KA, Kalantaridou SN, et al. Bone mineral density in young women with primary ovarian insufficiency: results of a three-year randomized controlled trial of physiological transdermal estradiol and testosterone replacement. J Clin Endocrinol Metab. 2014;99(9):3418-3426. doi:10.1210/jc.2013-4145 [PubMed 24905063]
  51. Progesterone injection [prescribing information]. Parsippany, NJ: Watson Pharma Inc; August 2018.
  52. Prometrium (progesterone) [prescribing information]. Langhorne, PA: Acertis Pharmaceuticals, LLC; December 2023.
  53. Prometrium (progesterone) [product monograph]. Kirkland, Quebec, Canada: Organon Canada Inc; March 2021.
  54. Ramalho I, Leite H, Águas F. Abnormal uterine bleeding in adolescents: a multidisciplinary approach. Acta Med Port. 2021;34(4):291-297. doi:10.20344/amp.12829 [PubMed 34214420]
  55. Refer to manufacturer's labeling.
  56. Reisman T, Goldstein Z. Case report: induced lactation in a transgender woman. Transgend Health. 2018;3(1):24-26. doi:10.1089/trgh.2017.0044 [PubMed 29372185]
  57. Romero R, Conde-Agudelo A, Da Fonseca E, et al. Vaginal progesterone for preventing preterm birth and adverse perinatal outcomes in singleton gestations with a short cervix: a meta-analysis of individual patient data. Am J Obstet Gynecol. 2018;218(2):161-180. doi:10.1016/j.ajog.2017.11.576 [PubMed 29157866]
  58. Rossouw JE, Anderson GL, Prentice RL, et al, “Risks and Benefits of Estrogen Plus Progestin in Healthy Postmenopausal Women: Principle Results From the Women's Health Initiative Randomized Controlled Trial,”JAMA, 2002, 288(3):321-33. [PubMed 12117397]
  59. Scali J, Ryan J, Carrière I, Dartigues JF, Tavernier B, Ritchie K, Ancelin ML. A prospective study of hormone therapy and depression in community-dwelling elderly women: the Three City Study. J Clin Psychiatry. 2010;71(12):1673-1679. doi:10.4088/JCP.09m05188blu [PubMed 20816026]
  60. Shumaker SA, Legault C, Rapp SR, et al, “Estrogen Plus Progestin and the Incidence of Dementia and Mild Cognitive Impairment in Postmenopausal Women: The Women's Health Initiative Memory Study: A Randomized Controlled Trial,” JAMA, 2003, 289(20):2651-62. [PubMed 12771112]
  61. Simons NE, Leeuw M, Van't Hooft J, et al. The long-term effect of prenatal progesterone treatment on child development, behaviour and health: a systematic review. BJOG. 2021;128(6):964-974. doi:10.1111/1471-0528.16582 [PubMed 33112462]
  62. Sophie Gibson ME, Fleming N, Zuijdwijk C, Dumont T. Where have the periods gone? The evaluation and management of functional hypothalamic amenorrhea. J Clin Res Pediatr Endocrinol. 2020;12(suppl 1):18-27. doi:10.4274/jcrpe.galenos.2019.2019.S0178 [PubMed 32041389]
  63. Standeven LR, McEvoy KO, Osborne LM. Progesterone, reproduction, and psychiatric illness. Best Pract Res Clin Obstet Gynaecol. 2020;69:108-126. doi:10.1016/j.bpobgyn.2020.06.001 [PubMed 32723604]
  64. Stuenkel CA, Davis SR, Gompel A, et al. Treatment of symptoms of the menopause: An Endocrine Society Clinical Practice Guideline. J Clin Endocrinol Metab. 2015;100(11):3975-4011. doi: 10.1210/jc.2015-2236. [PubMed 26444994]
  65. Sundström-Poromaa I, Comasco E, Sumner R, Luders E. Progesterone - Friend or foe? Front Neuroendocrinol. 2020;59:100856. doi:10.1016/j.yfrne.2020.100856 [PubMed 32730861]
  66. Tournaye H, Sukhikh GT, Kahler E, Griesinger G. A phase III randomized controlled trial comparing the efficacy, safety and tolerability of oral dydrogesterone versus micronized vaginal progesterone for luteal support in in vitro fertilization. Hum Reprod. 2017;32(5):1019-1027. doi:10.1093/humrep/dex023 [PubMed 28333318]
  67. US Department of Health and Human Services; Centers for Disease Control and Prevention; National Institute for Occupational Safety and Health. NIOSH list of antineoplastic and other hazardous drugs in healthcare settings 2016. https://www.cdc.gov/niosh/docs/2016-161/default.html. Updated September 2016. Accessed January 5, 2024.
  68. van der Linden M, Buckingham K, Farquhar C, Kremer JA, Metwally M. Luteal phase support for assisted reproduction cycles. Cochrane Database Syst Rev. 2015;2015(7):CD009154. doi:10.1002/14651858.CD009154.pub3 [PubMed 26148507]
  69. Wamboldt R, Shuster S, Sidhu BS. Lactation induction in a transgender woman wanting to breastfeed: case report. J Clin Endocrinol Metab. 2021;106(5):e2047-e2052. doi:10.1210/clinem/dgaa976 [PubMed 33513241]
  70. Warren MP, Biller BM, Shangold MM. A new clinical option for hormone replacement therapy in women with secondary amenorrhea: effects of cyclic administration of progesterone from the sustained-release vaginal gel Crinone (4% and 8%) on endometrial morphologic features and withdrawal bleeding. Am J Obstet Gynecol. 1999;180(1 Pt 1):42-48. doi:10.1016/s0002-9378(99)70147-x [PubMed 9914576]
  71. Wu H, Zhang S, Lin X, Wang S, Zhou P. Luteal phase support for in vitro fertilization/intracytoplasmic sperm injection fresh cycles: a systematic review and network meta-analysis. Reprod Biol Endocrinol. 2021;19(1):103. doi:10.1186/s12958-021-00782-5 [PubMed 34229723]
Topic 9817 Version 472.0

آیا می خواهید مدیلیب را به صفحه اصلی خود اضافه کنید؟