Get your patient on Lyleq - Norethindrone tablet (Norethindrone)

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Lyleq - Norethindrone tablet prescribing information

Indications & Usage

INDICATIONS AND USAGE

1. Indications

Progestin - only oral contraceptives are indicated for the prevention of pregnancy.

2. Efficacy

If used perfectly, the first-year failure rate for progestin - only oral contraceptives is 0.5%. However, the typical failure rate is estimated to be closer to 5%, due to late or omitted pills. The following table lists the pregnancy rates for users of all major methods of contraception.

Table 2: Percentage of Women Experiencing an Unintended Pregnancy During the First Year of Typical Use and the First Year of Perfect Use of Contraception and the Percentage Continuing Use at the End of the First Year. United States.
% of Women  Experiencing an
Unintended Pregnancy
within the First  Year of Use
% of Women  Continuing
Use at One Year 3
Method
(1)
Typical Use 1
(2)
Perfect Use 2
(3)
(4)
Chance 4
85
85
Spermicides 5
26
6
40
Periodic abstinence
25
63
Calendar
9
Ovulation Method
3
Sympto-Thermal 6
2
Post-Ovulation
1
Cap 7
Parous Women
40
26
42
Nulliparous Women
20
9
56
Sponge
Parous Women
40
20
42
Nulliparous Women
20
9
56
Diaphragm 7
20
6
56
Withdrawal
19
4
Condom 8
Female (Reality)
21
5
56
Male
14
3
61
Pill
5
71
Progestin only
0.5
Combined
0.1
IUDs
Progesterone T
2
1.5
81
Copper T380A
0.8
0.6
78
LNg20
0.1
0.1
81
Depo-Provera ®
0.3
0.3
70
Levonorgestrel Implants
(Norplant ® )
0.05
0.05
88
Female Sterilization
0.5
0.5
100
Male Sterilization
0.15
0.1
100

Emergency Contraceptive Pills

Treatment initiated within 72 hours after unprotected intercourse reduces the risk of pregnancy by at least 75%. 9

Lactational Amenorrhea Method


LAM is a highly effective, temporary method of contraception. 10

Source: Trussell, J, Contraceptive Efficacy. In: Hatcher RA, Trussell J, Stewart F, Cates W, Stewart GK, Kowal D, Guest F, Contraceptive Technology: Seventeenth Revised Edition. New York NY: Irvington Publishers, 1998.


  1. Among typical couples who initiate use of a method (not necessarily for the first time), the percentage who experience an accidental pregnancy during the first year if they do not stop use for any reason.
  2. Among couples who initiate use of a method (not necessarily for the first time), and who use it perfectly (both consistently and correctly), the percentage who experience an accidental pregnancy during the first year if they do not stop use for any other reason.
  3. Among couples attempting to avoid pregnancy, the percentage who continue to use a method for one year.
  4. The percentage of women becoming pregnant noted in columns (2) and (3) are based on data from populations where contraception is not used and from women who cease using contraception in order to become pregnant. Among such populations, about 89% become pregnant within one year. This estimate was lowered slightly (to 85%) to represent the percentage that would become pregnant within one year among women now relying on reversible methods of contraception if they abandoned contraception altogether.
  5. Foams, creams, gels, vaginal suppositories, and vaginal film.
  6. Cervical mucus (ovulation) method supplemented by calendar in the pre-ovulatory and basal body temperature in the post-ovulatory phases.
  7. With spermicidal cream or jelly.
  8. Without spermicides.
  9. The treatment schedule is one dose within 72 hours after unprotected intercourse, and a second dose 12 hours after the first dose. The Food and Drug Administration has declared the following brands of oral contraceptives to be safe and effective for emergency contraception: Ovral ® (1 dose is 2 white pills), Alesse ® (1 dose is 5 pink pills), Nordette ® or Levlen ® (1 dose is 4 yellow pills).
  10. However, to maintain effective protection against pregnancy, another method of contraception must be used as soon as menstruation resumes, the frequency or duration of breastfeeds is reduced, bottle feeds are introduced, or the baby reaches 6 months of age.
Dosage & Administration

DOSAGE AND ADMINISTRATION

To achieve maximum contraceptive effectiveness, Lyleq tablets must be taken exactly as directed. One tablet is taken every day, at the same time. Administration is continuous, with no interruption between pill packs. See PATIENT LABELING for detailed instructions.

Contraindications

CONTRAINDICATIONS

Progestin - only oral contraceptives (POPs) should not be used by women who currently have the following conditions:


  • Known or suspected pregnancy
  • Known or suspected carcinoma of the breast
  • Undiagnosed abnormal genital bleeding
  • Hypersensitivity to any component of this product
  • Benign or malignant liver tumors
  • Acute liver disease
Adverse Reactions

ADVERSE REACTIONS

  • Menstrual irregularity is the most frequently reported side effect.
  • Frequent and irregular bleeding are common, while long duration of bleeding episodes and amenorrhea are less likely.
  • Headache, breast tenderness, nausea, and dizziness are increased among progestin-only oral contraceptive users in some studies.
  • Androgenic side effects such as acne, hirsutism, and weight gain occur rarely.
Description

DESCRIPTION

Each light yellow to yellow Lyleq ® tablet provides a continuous oral contraceptive regimen of 0.35 mg norethindrone USP daily, and the inactive ingredients include corn starch, D&C Yellow No. 10 aluminum lake, FD&C Yellow # 6 aluminum lake, lactose monohydrate, magnesium stearate, povidone and talc.

The chemical name for norethindrone is 17-Hydroxy-19-Nor-17α-pregn-4-en-20-yn-3-one. The structural formula follows:
Referenced Image

Pharmacology

CLINICAL PHARMACOLOGY

1. Mode of Action

Lyleq progestin-only oral contraceptives prevent conception by suppressing ovulation in approximately half of users, thickening the cervical mucus to inhibit sperm penetration, lowering the mid-cycle LH and FSH peaks, slowing the movement of the ovum through the fallopian tubes, and altering the endometrium.

2. Pharmacokinetics

Absorption

Norethindrone is rapidly absorbed with maximum plasma concentrations occurring within 1 to 2 hours after Lyleq administration (see Table 1). Norethindrone appears to be completely absorbed following oral administration; however, it is subject to first pass metabolism resulting in an absolute bioavailability of approximately 65%.

Figure 1: Mean ± SD Norethindrone Plasma Concentrations Following Lyleq Administration

Referenced Image

Peak plasma concentrations occur approximately 1 hour after administration (mean T max 1.2 hours). The mean (SD) C max was 4816.8 (1532.6) pg/mL and generally occurred within 1 hour (mean) of tablet administration, ranging from 0.5 to 2 hours. The mean (SD) C avg was 885 (250) pg/mL, however, the mean concentration at 24 hrs was 130 (47) pg/mL.

Table 1 provides summary statistics of the pharmacokinetic parameters associated with single dose Lyleq administration.

Table 1: Mean ± SD Pharmacokinetic Parameters Following Single Dose Administration of Lyleq in 12 Healthy Female Subjects Under Fasting Conditions
Pharmacokinetic Parameter
Norethindrone 0.35 mg
T max (hr)
C max (pg/mL)
AUC (0 - 48) (pg·h/mL)
t½ (h)
1.2 ± 0.5
4817 ± 1533
21233 ± 6002
7.7 ± 0.5

The food effect on the rate and extent of norethindrone absorption after Lyleq administration has not been evaluated.

Distribution

Following oral administration, norethindrone is 36% bound to sex hormone-binding globulin (SHBG) and 61% bound to albumin. Volume of distribution of norethindrone is approximately 4 L/kg.

Metabolism

Norethindrone undergoes extensive biotransformation, primarily via reduction, followed by sulfate and glucuronide conjugation; less than 5% of a norethindrone dose is excreted unchanged; greater than 50% and 20 to 40% of a dose is excreted in urine and feces, respectively. The majority of metabolites in the circulation are sulfate, with glucuronides accounting for most of the urinary metabolites.

Excretion

Plasma clearance rate for norethindrone has been estimated to be approximately 600 L/day. Norethindrone is excreted in both urine and feces, primarily as metabolites. The mean terminal elimination half-life of norethindrone following single dose administration of Lyleq is approximately 8 hours.

How Supplied/Storage & Handling

HOW SUPPLIED

Lyleq (Norethindrone Tablets USP, 0.35 mg) are light yellow to yellow, round, flat faced beveled edge tablets, debossed with ‘S’ on one side and ‘14’ on other side of the tablet and are available in Blister Pack Containing 28 tablets.


The blister packs are available in the following packages:


•   The Blister Packs are packed in cartons


Carton of 1 Blister Pack                                           NDC 50102-300-11

Carton of 3 Blister Packs                                          NDC 50102-300-13


STORAGE


Store at controlled room temperature 20° to 25°C (68° to 77° F) [see USP Controlled Room Temperature].


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