Modafinil Package Insert

HIGHLIGHTS OF PRESCRIBING INFORMATION WARNINGS AND ... - Provigil
2 PROVIGIL® (modafinil) Tablets [C-IV] PROVIGIL® (modafinil) Tablets [C-IV] with fever and other abnormalities (e.g., vomiting, leukopenia). The median time to rash that resulted in discontinuation was 13 days. ... Access Doc

Www.accessdata.fda.gov
NDA 20-717 PROVIGIL® (modafinil) Tablets FDA Approved Labeling dated August 17, 2007 PROVIGIL® (modafinil) Tablets [C-IV] Rx Only DESCRIPTION PROVIGIL (modafinil) is a wakefulness-promoting agent for oral administration. Modafinil is a racemic compound. ... View This Document

Pharmacy Medical Necessity Guidelines: Analeptic CNS ...
Modafinil (Provigil) and armodafinil (Nuvigil) are indicated to improve wakefulness in patients with excessive daytime sleepiness associated with narcolepsy and shift work sleep disorder (SWSD), and for ... Access Content

Medical Department Procedure Manual - Home - AvMed
3.0 Medical Department staff has access to the Medical Department Procedure Manual and receives notice from management when procedures are developed, revised, or archived: Provigil® (modafinil) [package insert]. Frazer, PA: Cephalon, Inc. July 2008. ... Access Content

modafinil (Provigil )/armodafinil (Nuvigil
Modafinil (Provigil Nuvigil tablets [package insert]. Frazer, PA: Cephalon, Inc.; August 2013. 3. Veasey SC, Guilleminault C, Strohl KP, et al. Medical therapy for obstructive sleep apnea: a review by the medical therapy for ... Document Retrieval

DRUG Provigil (modafinil) - Connecticare.com
PHARMACY PRE-AUTHORIZATION CRITERIA DRUG Provigil (modafinil) REFERENCES 1. Provigil [package insert].West Chester, PA: Cephalon, Inc. 2. National Institutes of Health. National Heart, Lung, and Blood Institute. Sleep apnea: how is sleep apnea treated? ... Content Retrieval

Pharmacy Medical Necessity Guidelines: Nuvigil (modafinil)
3 Pharmacy Medical Necessity Guidelines: Nuvigil ® (armodafinil) & Provigil (modafinil) 4. The following quantity limitations apply to coverage. Please refer to the Pharmacy Medical Necessity Guidelines for Drugs with Quantity Limitations and submit a formulary exception request for those Members requiring higher quantities. ... Fetch Document

Cariprazine - Wikipedia
Cariprazine, sold under the brand names Vraylar in the United States and Reagila in Europe, is an atypical antipsychotic which is used in the treatment of schizophrenia and bipolar mania. It acts primarily as a D 3 receptor and D 2 receptor partial agonist , with high selectivity for the D 3 receptor. [2] ... Read Article

Euphorigenic And Abusive Properties Of Modafinil Chester, Pa ...
Able online (3). That letter specifically reiterates the package insert for modafinil, addressing its abuse potential and eu-phorigenic effects. That the euphorigenic side effects or abuse potential may be minimized has current treatment implications be-cause modafinil is increasingly promoted for fatigue and ... Read More

Provigil (modafinil) - Anthem
*NOTE: The quantity limit for Provigil 200mg tablets can be increased from 200mg (30 tablets/30 days) to 400mg (60 tablets/30 days) after a trial of 200mg (30 tablets/30 days) per day with no success. According to the package insert, doses of 400mg per day given as a ... Retrieve Content

Reference ID: 3685660
Reference ID: 3685660 rate of TEN and SJS associated with modafinil use, which is generally accepted to be an underestimate due to underreporting, exceeds the background incidence rate. ... Document Viewer

Modafinil Prior Authorization Request Form (Page 1 Of 2) DO ...
Is the prescribed dose higher than the maximum dose recommendation in FDA-approved labeling (i.e., the package insert)? Modafinil Prior Authorization Request Form (Page 2 of 2) DO NOT COPY FOR FUTURE USE. FORMS ARE UPDATED FREQUENTLY AND MAY BE BARCODED . ... Access Content

PROVIGIL / NUVIGIL (modafinil / Armodafinil) RATIONALE FOR ...
PROVIGIL / NUVIGIL (modafinil / armodafinil) RATIONALE FOR INCLUSION IN PA PROGRAM . Background . Provigil and Nuvigil are central nervous system stimulants and sharethe well-known potential for abuse of this class of drugs. The Drug Enforcement Administration (DEA) has rated Provigil and Nuvigil as Schedule IV drugs. ... Read More

Cli Inniccaall Ediitt ICCrritteerriiaa PPrrooppoossaall Drug ...
Cli inniccaall Ediitt iCCrritteerriiaa PPrrooppoossaall Drug/Drug Class: Narcolepsy Inhibitors Clinical Edit Date: • Claims for patients under 16 years of age for modafinil and <17 years of age for Package Insert for Xyrem, Jazz Pharmaceuticals, Inc., Philadelphia, PA 19103; ... Get Document

HIGHLIGHTS OF PRESCRIBING INFORMATION - Aptiom
FULL PRESCRIBING INFORMATION 1 INDICATIONS AND USAGE APTIOM is indicated for the treatment of partial-onset seizures in patients 4 years of age and older. ... Retrieve Content

Provigil And Nuvigil - HID
Provigil (Modafinil) Drugs requiring prior authorization: the list of drugs requiring prior authorization for this clinical edit Prior authorization criteria logic: a description of how the prior authorization request will be evaluated against the clinical edit criteria rules ... Retrieve Full Source

Focalin - Novartis US
Focalin® dexmethylphenidate hydrochloride tablets Rx only Prescribing Information DESCRIPTION Focalin® (dexmethylphenidate hydrochloride) is the d-threo-enantiomer of racemic methylphenidate hydrochloride, which is a 50/50 mixture of the d-threo and l-threo-enantiomers.Focalin is a central ... Read Document

Clinical Edit Criteria Proposal Provigil (Modafanil) And ...
• Claims for patients under 16 years of age for modafinil and <17 years of age for armodafinil (require clinical consultant review) • Patients do not meet approval criteria Package Insert for Provigil, Cephalon, Inc., Frazier, PA 19355; 2010. 4. ... Access Document

HIGHLIGHTS OF PRESCRIBING INFORMATION SWD INDICATIONS AND USAGE
1 indications and usage Modafinil Tablets are indicated to improve wakefulness in adult patients with excessive sleepiness associated with narcolepsy, obstructive sleep apnea (OSA), or shift work disorder (SWD). ... Retrieve Doc