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cyclosporine

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Overview

What is RESTASIS?

RESTASIS

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Structural Formula

Formula: CHNOMol. Wt.: 1202.6

Cyclosporine is a fine white powder. appears as a white opaque to slightly translucent homogeneous emulsion. It has an osmolality of 230 to 320 mOsmol/kg and a pH of 6.5-8.0. Each mL of ophthalmic emulsion contains: cyclosporine 0.05%. glycerin; castor oil; polysorbate 80; carbomer copolymer type A; purified water; and sodium hydroxide to adjust pH.



What does RESTASIS look like?



What are the available doses of RESTASIS?

Cyclosporine ophthalmic emulsion 0.5 mg/mL ()

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

How should I use RESTASIS?

RESTASIS

Invert the unit dose vial a few times to obtain a uniform, white, opaque emulsion before using. Instill one drop of ophthalmic emulsion twice a day in each eye approximately 12 hours apart. can be used concomitantly with lubricant eye drops, allowing a 15-minute interval between products. Discard vial immediately after use.


What interacts with RESTASIS?

Sorry No Records found


What are the warnings of RESTASIS?

Sorry No Records found


What are the precautions of RESTASIS?

Sorry No Records found


What are the side effects of RESTASIS?

Sorry No records found


What should I look out for while using RESTASIS?

RESTASIS


What might happen if I take too much RESTASIS?

Sorry No Records found


How should I store and handle RESTASIS?

Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]. Protect from moisture.RESTASIS30 Vials 0.4 mL each - NDC 0023-9163-3060 Vials 0.4 mL each - NDC 0023-9163-60Storage:RESTASIS30 Vials 0.4 mL each - NDC 0023-9163-3060 Vials 0.4 mL each - NDC 0023-9163-60Storage:RESTASIS30 Vials 0.4 mL each - NDC 0023-9163-3060 Vials 0.4 mL each - NDC 0023-9163-60Storage:RESTASIS30 Vials 0.4 mL each - NDC 0023-9163-3060 Vials 0.4 mL each - NDC 0023-9163-60Storage:


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Clinical Information

Chemical Structure

No Image found
Clinical Pharmacology

Cyclosporine is an immunosuppressive agent when administered systemically.

In patients whose tear production is presumed to be suppressed due to ocular inflammation associated with keratoconjunctivitis sicca, cyclosporine emulsion is thought to act as a partial immunomodulator. The exact mechanism of action is not known.

Non-Clinical Toxicology
RESTASIS

Potassium-sparing diuretics, angiotensin converting enzyme inhibitors (see ).

 Be careful not to touch the vial tip to your eye or other surfaces to avoid potential for eye injury and contamination.

The following serious adverse reactions are described elsewhere in the labeling:

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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

A total of 440 drugs (1549 brand and generic names) are known to interact with Imbruvica (ibrutinib). 228 major drug interactions (854 brand and generic names) 210 moderate drug interactions (691 brand and generic names) 2 minor drug interactions (4 brand and generic names) Show all medications in the database that may interact with Imbruvica (ibrutinib).