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norethindrone and ethinyl estradiol

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Overview

What is Kaitlib Fe?

Kaitlib Fe (norethindrone and ethinyl estradiol chewable tablets and ferrous fumarate chewable tablets) provides an oral contraceptive regimen consisting of 24 tablets that contain the active ingredients specified below, followed by four non-hormonal placebo tablets:

Each light green tablet also contains the following inactive ingredients: D&C yellow no. 10, FD&C blue no. 1, lactose monohydrate, magnesium stearate, mannitol, microcrystalline cellulose, povidone, sodium starch glycolate, sucralose, vitamin E and vanillin.

Each brown, round tablet contains ferrous fumarate, magnesium stearate, mannitol, microcrystalline cellulose, povidone, sodium starch glycolate, sucralose and vanillin. The ferrous fumarate chewable tablets do not serve any therapeutic purpose. Ferrous fumarate chewable tablets are not USP for dissolution and assay.

The empirical formula of ethinyl estradiol is CHO and the chemical structure is:

The chemical name of ethinyl estradiol is [19-Norpregna-1,3,5(10)-trien-20-yne-3,17- diol,(17α)-]

The empirical formula of norethindrone is CHO and the chemical structure is:

The chemical name of norethindrone is [17-hydroxy-19-nor-17α-pregn-4-en-20-yn-3-one]



What does Kaitlib Fe look like?



What are the available doses of Kaitlib Fe?

Kaitlib Fe (norethindrone and ethinyl estradiol chewable tablets and ferrous fumarate chewable tablets) is available in wallet.

Each wallet (28 tablets) contains in the following order:

What should I talk to my health care provider before I take Kaitlib Fe?

Nursing mothers: Not recommended, can decrease milk production. ()

How should I use Kaitlib Fe?

Chew one tablet without water at the same time every day. ()

Take tablets in the order directed on the wallet. ()


What interacts with Kaitlib Fe?

Sorry No Records found


What are the warnings of Kaitlib Fe?

Sorry No Records found


What are the precautions of Kaitlib Fe?

Sorry No Records found


What are the side effects of Kaitlib Fe?

Sorry No records found


What should I look out for while using Kaitlib Fe?

A high risk of arterial or venous thrombotic diseases. ()

Undiagnosed abnormal uterine bleeding. ()

Breast cancer or other estrogen- or progestin-sensitive cancer. ()

Liver tumors or liver disease. ()

Pregnancy. ()


What might happen if I take too much Kaitlib Fe?

There have been no reports of serious ill effects from overdose of oral contraceptives including ingestion by children. Overdosage may cause nausea, and withdrawal bleeding may occur in females.


How should I store and handle Kaitlib Fe?

Store at 20° to 25°C (68° to 77°F); excursions permitted from 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature]. Amoxicillin Tablets, USP 875 mg: Each film-coated tablet contains 875 mg amoxicillin as the trihydrate. Film-coated, capsule-shaped, pink tablet is scored on one side and imprinted WW951 on the other side. Dispense in a tight, light-resistant container as defined in the USP using a child resistant closure.


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Clinical Information

Chemical Structure

No Image found
Clinical Pharmacology

COCs lower the risk of becoming pregnant primarily by suppressing ovulation. Other possible mechanisms may include cervical mucus changes that inhibit sperm penetration and endometrial changes that reduce the likelihood of implantation.

Non-Clinical Toxicology
A high risk of arterial or venous thrombotic diseases. ()

Undiagnosed abnormal uterine bleeding. ()

Breast cancer or other estrogen- or progestin-sensitive cancer. ()

Liver tumors or liver disease. ()

Pregnancy. ()

Vascular risks: Stop Kaitlib Fe if a thrombotic event occurs. Stop at least 4 weeks before and through 2 weeks after major surgery. Start no earlier than 4 weeks after delivery in women who are not breastfeeding.()

Liver disease: Discontinue if jaundice occurs. ()

High blood pressure: Do not prescribe for women with uncontrolled hypertension or hypertension with vascular disease. ()

Carbohydrate and lipid metabolic effects: Monitor prediabetic and diabetic women taking Kaitlib Fe. Consider an alternate contraceptive method for women with uncontrolled dyslipidemia. ()

Headache: Evaluate significant change in headaches and discontinue if indicated. ()

Uterine bleeding: Evaluate irregular bleeding or amenorrhea. ()

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Reference

This information is obtained from the National Institute of Health's Standard Packaging Label drug database.
"https://dailymed.nlm.nih.gov/dailymed/"

While we update our database periodically, we cannot guarantee it is always updated to the latest version.

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Professional

Clonazepam Description Each single-scored tablet, for oral administration, contains 0.5 mg, 1 mg, or 2 mg Clonazepam, USP, a benzodiazepine. Each tablet also contains corn starch, lactose monohydrate, magnesium stearate, microcrystalline cellulose, and povidone. Clonazepam tablets USP 0.5 mg contain Yellow D&C No. 10 Aluminum Lake. Clonazepam tablets USP 1 mg contain Yellow D&C No. 10 Aluminum Lake, as well as FD&C Blue No. 1 Aluminum Lake. Chemically, Clonazepam, USP is 5-(o-chlorophenyl)-1,3-dihydro-7-nitro-2H-1,4-benzodiazepin-2-one. It is a light yellow crystalline powder. It has the following structural formula: C15H10ClN3O3 M.W. 315.72
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Interactions

Interactions

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