New Release: Alpha testing version has been released.

Estradiol

G03C - Estrogens ATC G03CA53 Small molecule approved 1975 Oral Topical Natural product Black-box warning

JFDA label: Femoston conti

⚠ Black-Box Warning
  • neurotoxicity — ChEMBL drug_warning (Black Box Warning) | United States
  • cardiotoxicity — ChEMBL drug_warning (Black Box Warning) | United States
  • vascular toxicity — ChEMBL drug_warning (Black Box Warning) | United States
  • carcinogenicity — ChEMBL drug_warning (Black Box Warning) | United States
  • respiratory toxicity — ChEMBL drug_warning (Black Box Warning) | United States
  • CIGARETTE SMOKING AND SERIOUS CARDIOVASCULAR EVENTS Cigarette smoking increases the risk of serious cardiovascular events from combination oral contraceptive (COC) use. This risk increases with age, p

Mechanism of Action

Agonist of Estrogen receptor — Estrogen receptor alpha agonist

TargetActionGene / class
Estrogen receptor efficacy AGONIST ESR1

Indications

Approved

  • Atrophic Vaginitis — Atrophic Vaginitis
  • Atrophy — Atrophy
  • Breast Neoplasms — breast carcinoma
  • Dyspareunia — Dyspareunia
  • Hypogonadism — hypogonadism
  • Menopause — menopause
  • Osteoporosis — osteoporosis
  • Osteoporosis, Postmenopausal — postmenopausal osteoporosis
  • Primary Ovarian Insufficiency — Premature ovarian insufficiency

Off-label

  • Aging
  • Alzheimer Disease
  • Amenorrhea
  • Anorexia Nervosa
  • Atherosclerosis
  • Bone Diseases, Metabolic
  • Bulimia Nervosa
  • Carcinoid Tumor
  • Coronary Disease
  • Depression, Postpartum
  • Depressive Disorder
  • Dry Eye Syndromes
  • Dysmenorrhea
  • Endometriosis
  • HIV Infections
  • Heart Diseases
  • Hereditary Breast and Ovarian Cancer Syndrome
  • Hot Flashes
  • Infertility
  • Migraine Disorders
  • Multiple Sclerosis
  • Myocardial Ischemia
  • Non-alcoholic Fatty Liver Disease
  • Obesity
  • Pain
  • Prostatic Neoplasms
  • Prostatic Neoplasms, Castration-Resistant
  • Psychotic Disorders
  • Schizophrenia
  • Severe Acute Respiratory Syndrome
  • Sexual Dysfunction, Physiological
  • Stress Disorders, Post-Traumatic
  • Triple Negative Breast Neoplasms
  • Turner Syndrome
  • Urinary Tract Infections

Contraindications

Source: openFDA

  • Oral contraceptives are contraindicated in women who currently have the following conditions: • Thrombophlebitis or thromboembolic disorders • A past history of deep vein thrombophlebitis or thromboembolic disorders • Cerebral vascular or coronary artery disease • Current diagnosis of, or history of, breast cancer, which may be hormone sensitive • Carcinoma of the endometrium or other known or suspected estrogen-dependent neoplasia • Undiagnosed abnormal genital bleeding • Cholestatic jaundice of pregnancy or jaundice with prior pill use • Hepatic adenomas or carcinomas • Are receiving Hepatitis C drug combinations containing ombitasvir/paritaprevir/ritonavir, with or without dasabuvir, due to the potential for ALT elevations (see WARNINGS , RISK OF LIVER ENZYME ELEVATIONS WITH CONCOMITANT HEPATITIS C TREATMENT ). Absolute

Dosing

Source: openFDA

The tablet dispenser has been designed to make oral contraceptive dosing as easy and as convenient as possible. The tablets are arranged in three rows of seven tablets each, with the days of the week appearing on the tablet dispenser above the first row of tablets. Note: Each tablet dispenser has been preprinted with the days of the week, starting with Sunday, to facilitate a Sunday-Start regimen. Six different day label strips have been provided with the Detailed Patient & Brief Summary Patient Package Insert in order to accommodate a Day-1 Start regimen. If the patient is using the Day-1 Start regimen, she should place the self-adhesive day label strip that corresponds to her starting day over the preprinted days. Important: The patient should be instructed to use an additional method of protection until after the first week of administration in the initial cycle when utilizing the Sunday-Start regimen. The possibility of ovulation and conception prior to initiation of use should be considered. Dosage and Administration for 21-Day Dosage Regimen To achieve maximum contraceptive effectiveness, Hailey 1.5/30 must be taken exactly as directed and at intervals not exceeding 24 hours. Hailey 1.5/30 provides the patient with a convenient tablet schedule of “3 weeks on-1 week off”. Two dosage regimens are described, one of which may be more convenient or suitable than the other for an individual patient. For the initial cycle of therapy, the patient begins her tablets according to the Day-1 Start or Sunday-Start regimen. With either regimen, the patient takes one tablet daily for 21 consecutive days followed by one week of no tablets. A. Sunday-Start Regimen: The patient begins taking tablets from the top row on the first Sunday after menstrual flow begins. When menstrual flow begins on Sunday, the first tablet is taken on the same day. The last tablet in the dispenser will then be taken on a Saturday, followed by no tablets for a week (7 days). For all subsequent cycles, the patient then begins a new 21-tablet regimen on the eighth day, Sunday, after taking her last tablet. Following this regimen, of 21 days on-7 days off, the patient will start all subsequent cycles on a Sunday. B. Day-1 Regimen: The first day of menstrual flow is Day 1. The patient places the self-adhesive day label strip that corresponds to her starting day over the preprinted days on the tablet dispenser. She starts taking one tablet daily, beginning with the first tablet in the top row. The patient completes her 21-tablet regimen when she has taken the last tablet in the tablet dispenser. She will then take no tablets for a week (7 days). For all subsequent cycles, the patient begins a new 21-tablet regimen on the eighth day after taking her last tablet, again starting with the first tablet in the top row after placing the appropriate day label strip over the preprinted days on the tablet dispenser. Following this regimen of 21 days on-7 days off, the patient will start all subsequent cycles on the same day of the week as the first course. Likewise, the interval of no tablets will always start on the same day of the week. Tablets should be taken regularly with a meal or at bedtime. It should be stressed that efficacy of medication depends on strict adherence to the dosage schedule. Special Notes on Administration Menstruation usually begins two or three days, but may begin as late as the fourth or fifth day, after discontinuing medication. If spotting occurs while on the usual regimen of one tablet daily, the patient should continue medication without interruption. If the patient forgets to take one or more tablets, the following is suggested: One tablet is missed • take tablet as soon as remembered • take next tablet at the regular time Two consecutive tablets are missed (week 1 or week 2) • take two tablets as soon as remembered • take two tablets the next day • use another birth control method for seven days following the missed tablets Two consecutive tab

Warnings & Precautions

Source: openFDA

Boxed Warning

CIGARETTE SMOKING AND SERIOUS CARDIOVASCULAR EVENTS Cigarette smoking increases the risk of serious cardiovascular events from combination oral contraceptive (COC) use. This risk increases with age, particularly in women over 35 years of age, and with the number of cigarettes smoked. For this reason, COCs, including Hailey 1.5/30, are contraindicated in women who are over 35 years of age and smoke (see CONTRAINDICATIONS and WARNINGS ).

Warnings & Precautions

The use of oral contraceptives is associated with increased risks of several serious conditions including myocardial infarction, thromboembolism, stroke, hepatic neoplasia, and gallbladder disease, although the risk of serious morbidity or mortality is very small in healthy women without underlying risk factors. The risk of morbidity and mortality increases significantly in the presence of other underlying risk factors such as hypertension, hyperlipidemias, obesity, and diabetes. Practitioners prescribing oral contraceptives should be familiar with the following information relating to these risks. The information contained in this package insert is principally based on studies carried out in patients who used oral contraceptives with higher formulations of estrogens and progestogens than those in common use today. The effect of long-term use of the oral contraceptives with lower formulations of both estrogens and progestogens remains to be determined. Throughout this labeling, epidemiological studies reported are of two types: retrospective or case control studies and prospective or cohort studies. Case control studies provide a measure of the relative risk of a disease, namely, a ratio of the incidence of a disease among oral contraceptive users to that among nonusers. The relative risk does not provide information on the actual clinical occurrence of a disease. Cohort studies provide a measure of attributable risk, which is the difference in the incidence of disease between oral contraceptive users and nonusers. The attributable risk does provide information about the actual occurrence of a disease in the population (adapted from References 8 and 9 with the author’s permission). For further information, the reader is referred to a text on epidemiological methods. 1. Thromboembolic Disorders and Other Vascular Problems a. Myocardial infarction An increased risk of myocardial infarction has been attributed to oral contraceptive use. This risk is primarily in smokers or women with other underlying risk factors for coronary artery disease such as hypertension, hypercholesterolemia, morbid obesity, and diabetes. The relative risk of heart attack for current oral contraceptive users has been estimated to be two to six (10 - 16). The risk is very low under the age of 30. Smoking in combination with oral contraceptive use has been shown to contribute substantially to the incidence of myocardial infarctions in women in their mid-thirties or older with smoking ac

Oral contraceptives non-smoker** 0.3 0.5 0.9 1.9 13.8

Oral contraceptives non-smoker** 0.3 0.5 0.9 1.9 13.8

Oral contraceptives smoker** 2.2 3.4 6.6 13.5 51.1

Oral contraceptives smoker** 2.2 3.4 6.6 13.5 51.1

IUD** 0.8 0.8 1 1 1.4

IUD** 0.8 0.8 1 1 1.4

Condom* 1.1 1.6 0.7 0.2 0.3

Condom* 1.1 1.6 0.7 0.2 0.3

Diaphragm/spermicide* 1.9 1.2 1.2 1.3 2.2

Diaphragm/spermicide* 1.9 1.2 1.2 1.3 2.2

Periodic abstinence* 2.5 1.6 1.6 1.7 2.9 3.6 *Deaths are birth related

Periodic abstinence* 2.5 1.6 1.6 1.7 2.9 3.6 *Deaths are birth related. **Deaths are method related Adapted from H.W. Ory, Reference 41. 3. Malignant Neoplasms Breast Cancer Norethindrone acetate and ethinyl estradiol tablets are contraindicated in females who currently have or have had breast cancer because breast cancer may be hormonally sensitive (see CONTRAINDICATIONS ). Epidemiology studies have not found a consistent association between use of combined oral contraceptives (COCs) and breast cancer risk. Studies do not show an association between ever (current or past) use of COCs and risk of breast cancer. However, some studies report a small increase in the risk of breast cancer among current or recent users (<6 months since last use) and current users with longer duration of COC use (see ADVERSE REACTIONS , Postmarketing Experience). Cervical Cancer Some studies suggest that oral contraceptive use has been associated with an increase in the risk of cervical intraepithelial neoplasia in some populations of women (42-45). However, there continues to be controversy about the extent to which such findings may be due to differences in sexual behavior and other factors. 4. Hepatic Neoplasia Benign hepatic adenomas are associated with oral contraceptive use, although the incidence of benign tumors is rare in the United States. Indirect calculations have estimated the attributable risk to be in the range of 3.3 cases/100,000 for users, a risk that increases after four or more years of use (46). Rupture of rare, benign, hepatic adenomas may cause death through intra-abdominal hemorrhage (47,48). Studies from Britain have shown an increased risk of developing hepatocellular carcinoma (49 - 51) in long-term (greater than 8 years) oral contraceptive users. However, these cancers are extremely rare in the U.S., and the attributable risk (the excess incidence) of liver cancers in oral contraceptive users approaches less than one per million users. 5. Risk of Liver Enzyme Elevations with Concomitant Hepatitis C Treatment During clinical trials with the Hepatitis C combination drug regimen that contains ombitasvir/paritaprevir/ritonavir, with or without dasabuvir, ALT elevations greater than 5 times the upper limit of normal (ULN), including some cases greater than 20 times the ULN, were significantly more frequent in women using ethinyl estradiol-containing medications such as COCs. Discontinue norethindrone acetate and ethinyl estradiol tablets prior to starting

Pregnancy & Lactation

Pregnancy

Lactation

Caution Hale L3

Maternal doses of up to 200 mcg daily transdermally do not increase estradiol or estriol in breastfed infants or cause any adverse

Chemistry & Properties

2D structure
FormulaC18H24O2
Molecular weight272.39 g/mol
IUPAC name(8R,9S,13S,14S,17S)-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,17-diol
CAS50-28-2
PubChem CID5757
InChIKeyVOXZDWNPVJITMN-ZBRFXRBCSA-N
logP3.61 (XLogP 4.0)
Polar surface area40.46 Ų
H-bond acceptors / donors2 / 2
Drug-likeness (QED)0.76
Lipinski violations0
SMILESC[C@]12CC[C@@H]3c4ccc(O)cc4CC[C@H]3[C@@H]1CC[C@@H]2O

Biology & Pharmacokinetics

Pharmacokinetics predicted

Bioavailability70.0%
Half-life1.686 h
Volume of distribution1.041 L/kg
Protein binding86.6%
BBB penetrantYes

Enzyme interactions

EnzymeRoleDetail
CYP1A2Substrate
CYP2B6Inhibitor
CYP2B6Substrate
CYP2C19Substrate
CYP2C8Inhibitor
CYP2C9Substrate
CYP2D6Substrate

Receptor binding (top 9)

TargetActionAffinity
estrogen beta Binding pKi 10.0
estrogen alpha Binding pKi 9.9
Estrogen receptor-&alpha; (ESR1) Agonist pKi 9.8
Estrogen receptor-&beta; (ESR2) Agonist pKi 9.3
Estrogen receptor beta (ESR2) Binding pKi 8.7
Estrogen receptor alpha (ESR1) Binding pKi 8.3
estrogen, ER alpha Binding pKi 6.4
estrogen, ER beta Binding pKi 5.7
KCa1.1 (KCNMA1) Activator pEC50 5.6

Transporters

BCRP (Inhibitor)BCRP (Inhibitor)BSEP (Inhibitor)BSEP (Inhibitor)MATE1 (Inhibitor)MATE2 (Inhibitor)MRP (Inhibitor)MRP1 (Inhibitor)MRP4 (Inhibitor)MRP7 (Inhibitor)OAT1 (Inhibitor)OAT3 (Inhibitor)OAT4 (Inhibitor)OATP1A2 (Inhibitor)OATP1B1 (Inhibitor)OATP1B1 (Inhibitor)OATP1B3 (Inhibitor)OATP1B3 (Inhibitor)OATP2B1 (Inhibitor)OCT1 (Inhibitor)OCT2 (Inhibitor)OCT3 (Inhibitor)P-gp (Inhibitor)BCRP (Substrate)MDR1 (Substrate)MRP2 (Substrate)MRP3 (Substrate)OATP (Substrate)OATP1B1 (Substrate)OATP1B2 (Substrate)OATP1B3 (Substrate)P-gp (Substrate)

Drug–drug interactions (100+, DDInter)

Interacting drugSeverityManagement
Carfilzomib major
Hemin major
Lenalidomide major
Pomalidomide major
Thalidomide major
Tranexamic acid major
Acarbose moderate
Acetohexamide moderate
Albiglutide moderate
Alogliptin moderate
Amikacin moderate
Amikacin (liposome) moderate
Aminoglutethimide moderate
Aminophylline moderate
Amoxicillin moderate
Anastrozole moderate
Apalutamide moderate
Aprepitant moderate
Bacitracin moderate
Betamethasone moderate
Bexarotene moderate
Brigatinib moderate
Budesonide moderate
Calcipotriol (topical) moderate
Calcitriol (topical) moderate
Canagliflozin moderate
Chenodeoxycholic acid moderate
Chloramphenicol moderate
Chlorpropamide moderate
Clarithromycin moderate
Clindamycin moderate
Clotrimazole moderate
Cobicistat moderate
Conestat alfa moderate
Corticotropin moderate
Cyclosporine moderate
Dabrafenib moderate
Dapagliflozin moderate
Dasatinib moderate
Deferasirox moderate

Showing 40 of 100+.

Registered Products (8)

BrandForm / strengthPackAgentCitizen (JOD)
PROGYLUTON Tab Tablet 0.5 mg, 2 mg 21 tab The Jordan Drugstore Co 1.520
Climen Tab Tablet 1 mg, 2 mg 21 tab The Jordan Drugstore Co 4.870
TRISEQUENS TABS Tablet 2, 2, 1 mg, 0, 1, 0 mg 2 mg Khoury Drug Store 4.890
Estrofem Tablet Tablet 2 mg 28 tab Khoury Drug Store 5.300
Kliogest Tablet Tablet 1 mg, 2 mg 28 tab Khoury Drug Store 5.320
Femoston Tab Tablet 2 mg, 10 mg 3X28 Khraim Drug Store 17.140
Vagifem 10 mcg Vag Tab Tablet 10 mcg 18 applicators with Insert Tabs Khoury Drug Store 17.290
Femoston conti Tablet 1 mg, 5 mg 28 tab Khraim Drug Store 19.050