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Search result(s) may include information that is not consistent with the product’s Full Prescribing Information. Eisai does not recommend any use that is inconsistent with the Full Prescribing Information. Search result(s) containing information about investigational uses does not imply FDA approval for these uses, nor does it establish the safety or efficacy of these uses. There is no guarantee that the investigational uses will receive FDA approval.
LEQEMBI® (lecanemab-irmb) is approved only for the indication and dosages that appear in the LEQEMBI full Prescribing Information. The information below and/or its appendices may summarize publications or guidelines that describe indications or treatment modalities for the use of LEQEMBI that have not been approved by the Food and Drug Administration.
LEQEMBI is an amyloid beta-directed antibody indicated for the treatment of Alzheimer’s disease. Treatment with LEQEMBI should be initiated in patients with mild cognitive impairment or mild dementia stage of disease, the population in which treatment was initiated in clinical trials.
Adverse reactions, some of which can be serious or fatal, may occur with LEQEMBI, including Amyloid Related Imaging Abnormalities (ARIA), Infusion-Related Reactions, and Hypersensitivity Reactions. For Important Safety Information, including Boxed WARNING regarding ARIA, please click here: Important Safety Information.
For full Prescribing Information for LEQEMBI, including Boxed WARNING, please VIEW/DOWNLOAD
Please note that DAYVIGO (lemborexant) CIV is approved only for those indications and dosages that appear in the DAYVIGO Full Prescribing Information. The information below and/or its appendices may summarize publications or guidelines that describe indications or treatment modalities for the use of DAYVIGO that have not been approved by the Food and Drug Administration.
The information below is provided by Eisai Inc. and is intended to assist you in forming your own clinical conclusions regarding the use of Eisai products. Eisai Inc. does not recommend or endorse the use of this product in any manner other than as described in the Full Prescribing Information.
DAYVIGO is contraindicated in patients with narcolepsy. Adverse reactions, some of which can be serious or fatal, may occur with DAYVIGO, including Central Nervous System (CNS) depressant effects and daytime impairment, sleep paralysis, hynagogic/hypnopompic hallucinations and cataplexy-like symptoms, complex sleep behaviors and worsening of depression/suicidal ideation. The effect of DAYVIGO on respiratory function should be considered for patients with compromised respiratory function. Treatment of insomnia should be initiated only after careful evaluation for comorbid diagnoses. Click here for Important Safety Information.
DAYVIGO is an orexin receptor antagonist indicated for the treatment of adult patients with insomnia, characterized by difficulties with sleep onset and/or sleep maintenance.
Prescribing Information for DAYVIGO® (lemborexant) CIV VIEW/DOWNLOAD
Prescribing Information for LEQEMBI® (lecanemab-irmb), including Boxed WARNING VIEW/DOWNLOAD
Prescribing Information for DAYVIGO® (lemborexant) CIV VIEW/DOWNLOAD
Prescribing Information for BANZEL® (rufinamide): VIEW/DOWNLOAD
Please note that Banzel is approved for those indications and dosages that appear in the enclosed Banzel Full Prescribing Information. The enclosed information and/or its appendices may summarize publications or guidelines that describe indications or treatment modalities for the use of Banzel that have not been approved by the Food and Drug Administration.
The enclosed information is provided by Eisai Inc. and is intended to assist you in forming your own clinical conclusions regarding Eisai products. Eisai Inc. does not recommend or endorse the use of this product in any manner other than as described in the Full Prescribing Information.
Click here for Important Safety Information.
Prescribing Information for BANZEL® (rufinamide): VIEW/DOWNLOAD
Eisai does not recommend or endorse the use of this investigational agent in any manner as it has not been approved by the U.S. Food and Drug Administration. This information discusses investigational uses of an agent in development and is not intended to convey conclusions about efficacy, safety, or appropriate use. There is no guarantee that such agent will successfully complete clinical development or gain health authority approval. Please do not distribute or copy the attached information. Please refine your search criteria or submit a medical inquiry
Eisai does not recommend or endorse the use of this investigational agent in any manner as it has not been approved by the U.S. Food and Drug Administration. This information discusses investigational uses of an agent in development and is not intended to convey conclusions about efficacy, safety, or appropriate use. There is no guarantee that such agent will successfully complete clinical development or gain health authority approval. Please do not distribute or copy the attached information. Please refine your search criteria or submit a medical inquiry
Eisai does not recommend or endorse the use of this investigational agent in any manner as it has not been approved by the U.S. Food and Drug Administration. This information discusses investigational uses of an agent in development and is not intended to convey conclusions about efficacy, safety, or appropriate use. There is no guarantee that such agent will successfully complete clinical development or gain health authority approval. Please do not distribute or copy the attached information. Please refine your search criteria or submit a medical inquiry
Eisai does not recommend or endorse the use of this investigational agent in any manner as it has not been approved by the U.S. Food and Drug Administration. This information discusses investigational uses of an agent in development and is not intended to convey conclusions about efficacy, safety, or appropriate use. There is no guarantee that such agent will successfully complete clinical development or gain health authority approval. Please do not distribute or copy the attached information. Please refine your search criteria or submit a medical inquiry
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