FDA - Adverse Event Reporting System (FAERS)
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1 Case Information: Case Type: EXPEDITED (5- DAY) esub: Y HP: Country: USA Outcomes: DE, (A)NDA/BLA: / FDA Rcvd Date: 09-Oct-204 Mfr Rcvd Date: 08-Oct-204 Mfr Control : GB-ELI_LILLY_AND_COMPANY-US890360A Patient Information: Age: 47 YR Sex: Male Weight: Suspect Products: Product Name Dose/ Frequency Route Dosage Text Indications(s) Start Date End Date PROZAC 20 MG/ Oral 20 mg, unknown Depression 0-Aug-989 -Sep-989 Interval st Product Name Dose to Event DeC ReC Lot Exp Date NDC MFR/Labeler PROZAC 36 Day A ELI LILLY AND CO Event Information: Preferred Term ( MedDRA Â Version: Aggression Agitation Fatigue Homicide Insomnia Suicide attempt Tangentiality 7.0 ) ReC Print Time: 25-AUG-205 0:05 AM If a field is blank, there is no data for that field Page 245 of 533
2 Event/Problem Narrative: PATIENT ENTERED HIS AND SHOT BEFORE SHOOTING HIMSELF. PRIOR TO THE SHOOTINGS, THE PATIENT HAD BEEN SEEN BY HIS PSYCHIATRIST AND EXHIBITED "TANGENTIAL THOUGHTS" AND "INCREASED LEVEL OF AGITATION AND ANGER." PATIENT * *CONT FROM SEC 7* PZ REPORTEDLY WAS D/C 3 DAYS PRIOR TO SHOOTING.PT PREVIOUSLY TAKEN PZ IN 988 BUT STOPPED TX DUE TO FATIGUE. COPY OF AND02689 NEWSPAPER ARTICLES ATTACHED. CORONER(DR. )PROVIDED ADDT'L INFO IN PHONE CONVERSATION NEWSPAPER ARTICLE MENTIONED POSSIBLE PZ ASS'N. 030 CONVERSATION W CORONER PROVIDED REPORTED BLOOD LEVELS. F/U 689: COPY OF HOSP SUMMARY FROM THE CORONER'S ATTACHED. IF FURTHER INFO RETOX OR AUTOPSY DATA BECOMES AVAILABLE, WE WILL FORWARD. **CONT'D FROM SEC. 23** 2 PREVIOUS HOSPITALIZATIONS THAT HE MIGHT LIKE TO PREVIOUS DX,IN ADDT'N TO MANIC DEPRESSIVE, INC BORDERLINE PERSONALITY W PARANOID FEATURES, DYSTHYMIC DISORDER W PARANOID TYPE PERSONALITY. F/U 2589: AUTOPSY REPORT ATTACHED. F/U /9/90: PER DR., CORONER:PT'S TIME OF DEATH APPROX. 8:40AM, HIS AUTOPSY STARTED AT 5:0 PM. BLOOD LEVELS 5:20 PM.SITE FROM WHICHSAMPLE WAS COLLECTED WAS FROM THE HEART. F/U 7/26/90: MORE THAN A YEAR BEFORE THIS ASSAULT, PT HAD BROUGHT THIS REPORT WAS FOUND TO HAVE A DUPLICATE, US940644A, WHICH WILL BE DELETED. F/U 23NOV94: PATIENT EXPERIENCED INSOMNIA WHILE ON PROZAC. THIS IS FOUR OF FOUR CASES ALSO DESCRIBED IN THE ARTICLE: HAND J, TOBIN D. PROZAC DEFENSE MAY DEBUT IN CNY. THE POST-STANDARD. SUNDAY, NOVEMBER 7, SEE US_ , US_ AND US950864A. THIS CASE WAS ALSO DESCRIBED IN THE FOLLOWING ARTICLE: LENZER J. FDA TO REVIEW "MISSING" DRUG COMPANY DOCUMENTS. BRITISH MEDICAL JOURNAL. 0JAN2005. THE FOLLOWING ARTICLES REPORTED ON THE ABOVE BMJ PUBLICATION THAT DESCRIBED THIS CASE:. Print Time: 25-AUG-205 0:05 AM If a field is blank, there is no data for that field Page 246 of 533
3 EDIT 04-DEC-2002: ADDITIONAL INFORMATION RECEIVED IN THE LITERATURE (NEWSPAPER) ON 25- NOV ADDED NON HEALTH CARE PROVIDER REPORTER AND LOCAL ID OF "LIT." ADDED LITERATURE CITATION TO NARRATIVE PAGE. ON SUSPECT DRUG PAGE ENTERED DRUG TYPE AND ANSWERED EXPOSURE CONDITIONS OF HEPATIC AND RENAL IMPAIRED. EDIT 0JAN05: UPDATED NARRATIVE PAGE TO ADD EIGHT LITERATURE CITATIONS. UPDATE 30-NOV-2006: IT WAS NOTED ON 2-NOV-2006, IN THE ARTICLE, BY HEALY, D, HERXHEIMER, A, MENKES, D, THAT THIS CASE WAS DISCUSSED. NO NEW MEDICALLY SIGNIFICANT INFORMATION WAS PROVIDED. THE SOURCE OF THE CASE WAS CHANGED FROM SPONTANEOUS TO LITERATURE. LITERATURE CITATION WAS ADDED. SEE ALSO, CASES DISCUSSED IN THE ARTICLE; GB AND US962359A. THIS CASE WAS DESCRIBED IN THE ARTICLES: HEALY, D, HERXHEIMER, A, MENKES, D. ANTIDEPRESSANTS AND VIOLENCE: PROBLEMS AT THE INTERFACE OF MEDICINE AND LAW. PLOS MEDICINE. 2006;3(9), , AND HEALY, D, HERXHEIMER, A, MENKES, D. ANTIDEPRESSANTS AND VIOLENCE: PROBLEMS AT THE INTERFACE OF MEDICINE AND LAW. INTERNATIONAL JOURNAL OF RISK AND SAFETY IN MEDICINE. 2007; 9: Rokuro Hama. Harmful effects of medicines; Harmful effects of selective serotonin reuptake inhibitor (SSRI). Check up your medicine Not Reported. Medication- Induced violence towards others. Prescrire International. 23 (50) (pp 53-55), 204. Not Reported. IRS antidepressants and violence. Rev Prescrire, 2008; 28(296): UPDATE 05-DEC-2006: UPON REVIEW OF CASE NOTED THAT LISTEDNESS WAS SHOWING AS "UNKNOWN" FOR MOST OF THE EVENTS AND THERE WAS NO PSUR COMMENT. LISTEDNESS ADDED FOR EVENTS AND PSUR COMMENT ADDED. UPDATE 25JAN2008: DUPLICATE ARTICLE BY THE SAME AUTHORS IN A DIFFERENT JOURNAL RECEIVED ON 22JAN2008. ADDED REPORTER AND CITATION INFORMATION. UPDATED NARRATIVE. Update 23Jan204: A new citation was received on 2Jan204. Added citation to narrative and added author; no new clinical information was added to the case. Print Time: 25-AUG-205 0:05 AM If a field is blank, there is no data for that field Page 247 of 533
4 Edit 30JAN204: Edit performed to amend E2B Company number to reflect country of case. No other changes. Edit 3Jan204: Upon internal review, for submission purposes added suspect drug action taken, added the as reported descriptions for the coded events of agitation and insomnia. Edit 03Feb204: Upon internal review, removed onset date for event of fatigue as med sig edit. Update 6Sep204. A new citation was received on 5Sep204; no new clinical information was added Update 08Oct204: Additional citation received on 08Oct204 via a literature search from another article; no new clinical information added. Relevant Medical History: Disease/Surgical Procedure Start Date End Date Continuing? Medical History Product(s) Start Date End Date Indications Events Relevant Laboratory Data: Test Name Result Unit Normal Low Range Normal High Range Info Avail Concomitant Products: 2 3 Product Name LITHIUM TEMAZEPAM TRAZODONE Dose/ Frequency Route Dosage Text Indications(s) Start Date End Date Interval st Dose to Event TID UNK, 3/D UNK, unknown UNK, other Print Time: 25-AUG-205 0:05 AM If a field is blank, there is no data for that field Page 248 of 533
5 Reporter Source: Study Report?: No Sender Organization: ELI LILLY AND CO Literature Text: Healy, D, Herxheimer, A, Menkes, D..Antidepressants and Violence: Problems at the Interface of Medicine and Law..PLoS Medicine. 2006;3(9): Print Time: 25-AUG-205 0:05 AM If a field is blank, there is no data for that field Page 249 of 533
FDA Adverse Event Reporting System (FAERS) FOIA Case Report Information
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