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Learn if You Have a Claim Against Eli Lilly & Co.

FDA, Eli Lilly Updates Labeling for Strattera To Include Suicidal Thinking in Children

The FDA directed Eli Lilly and Company, the manufacturer of Strattera (atomoxetine), to revise the prescribing information to include a boxed warning and additional warning statements that alert health care providers of an increased risk of suicidal thinking in children and adolescents being treated with this medication. FDA also informed Lilly that a Patient Medication Guide (MedGuide) should be provided to patients when Strattera is dispensed. The MedGuide advises patients of the risks associated with and precautions that can be taken when Strattera is dispensed.

Claimant Information

Are you submitting this information on behalf of yourself? Yes  No
Are you submitting this information on behalf of an adolescent child? Yes  No
If yes, please provide: Name of Child
   Age of Child
   Relationship to Child

Strattera Use

Was the Strattera user an adolescent at the time of use? Yes  No
Date you began taking Strattera:
Date you stopped taking Strattera:

Medical Information

Did the Strattera user commit or attempt suicide? Yes  No
If yes please explain:
Date of suicide or attempt:
City in which suicide or attempt occurred:
State in which suicide or attempt occurred:
Did the Strattera user attempt suicide prior to the use of the Strattera? Yes  No
If yes, please explain:
Are you presently covered by health insurance? Yes  No
Have you previously retained an attorney to represent you in this matter? Yes  No

Personal Information

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