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Ella

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Overview

What is Ella?

The ella (ulipristal acetate) tablet for oral use contains 30 mg of a single active steroid ingredient, ulipristal acetate [17α-acetoxy-11β-(4-N,N-dimethylaminophenyl)-19-norpregna-4,9-diene-3,20-dione], a synthetic progesterone agonist/antagonist. The inactive ingredients are lactose monohydrate, povidone K-30, croscarmellose sodium and magnesium stearate.

Ulipristal acetate is a white to yellow crystalline powder which has a molecular weight of 475.6. The structural formula is:

                           CHNO



What does Ella look like?



What are the available doses of Ella?

The tablet is supplied as a white to off-white, round, curved tablet containing 30 mg of ulipristal acetate and is marked "" on both sides.

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

How should I use Ella?

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Instruct patients to take one tablet orally as soon as possible within 120 hours (5 days) after unprotected intercourse or a known or suspected contraceptive failure.

The tablet can be taken with or without food.

If vomiting occurs within 3 hours of intake, consideration should be given to repeating the dose.

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What interacts with Ella?

Sorry No Records found


What are the warnings of Ella?

Sorry No Records found


What are the precautions of Ella?

Sorry No Records found


What are the side effects of Ella?

Sorry No records found


What should I look out for while using Ella?

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See

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What might happen if I take too much Ella?

Experience with ulipristal acetate overdose is limited. In a clinical study, single doses equivalent to up to 4 times were administered to a limited number of subjects without any adverse reactions.


How should I store and handle Ella?

Store at 20º to 25ºC (68º to 77ºF); excursions permitted to 15º to 30ºC (59º to 86ºF) [see USP Controlled Room Temperature].ellaellaNDC 50102-911-01 (1 tablet unit of use package)Store at 20-25°C (68-77°F). [See USP controlled room temperature.]Keep the blister in the outer carton in order to protect from light. .ellaellaNDC 50102-911-01 (1 tablet unit of use package)Store at 20-25°C (68-77°F). [See USP controlled room temperature.]Keep the blister in the outer carton in order to protect from light. .ellaellaNDC 50102-911-01 (1 tablet unit of use package)Store at 20-25°C (68-77°F). [See USP controlled room temperature.]Keep the blister in the outer carton in order to protect from light. .ellaellaNDC 50102-911-01 (1 tablet unit of use package)Store at 20-25°C (68-77°F). [See USP controlled room temperature.]Keep the blister in the outer carton in order to protect from light. .ellaellaNDC 50102-911-01 (1 tablet unit of use package)Store at 20-25°C (68-77°F). [See USP controlled room temperature.]Keep the blister in the outer carton in order to protect from light. .


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Clinical Information

Chemical Structure

No Image found
Clinical Pharmacology

When taken immediately before ovulation is to occur,  postpones follicular rupture. The likely primary mechanism of action of ulipristal acetate for emergency contraception is therefore inhibition or delay of ovulation; however, alterations to the endometrium that may affect implantation may also contribute to efficacy. 

Non-Clinical Toxicology
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See

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Aminoglutethimide:

Amphotericin B injection and potassium-depleting agents:





Anticholinesterases:

Anticoagulants, Oral:

Antidiabetics:

Antitubercular Drugs:

Cholestyramine:

Cyclosporine:

Dexamethasone Suppression Test (DST):

Digitalis Glycosides:

Ephedrine:

Estrogens, including Oral Contraceptives:

Hepatic Enzyme Inducers, Inhibitors and Substrates:

Ketoconazole:

Nonsteroidal Anti-Inflammatory Agents (NSAIDS):

Phenytoin:

Skin Tests:

Thalidomide:





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A web-based study has been established to collect information on the pregnancy outcomes of women who inadvertently receive during the cycle in which pregnancy started or at anytime during pregnancy.

Enroll your patient by completing the forms available at where voluntary reports from health care providers or consumers are received.

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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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Tips

Tips

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Interactions

Interactions

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