The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
125667822 12566782 2 F 20160623 20160725 20160718 20160727 EXP FR-ELI_LILLY_AND_COMPANY-FR201607004386 ELI LILLY AND CO 49.94 YR F Y 0.00000 20160727 CN FR FR

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
125667822 12566782 1 PS PROZAC FLUOXETINE HYDROCHLORIDE 1 Oral UNK U U 18936
125667822 12566782 2 SS URBANYL CLOBAZAM 1 Oral 750 MG, SINGLE U U 0 750 MG TABLET
125667822 12566782 3 SS XANAX ALPRAZOLAM 1 Oral UNK U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125667822 12566782 1 Product used for unknown indication
125667822 12566782 2 Product used for unknown indication
125667822 12566782 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125667822 12566782 LT
125667822 12566782 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125667822 12566782 Coma
125667822 12566782 Hypotension
125667822 12566782 Poisoning deliberate
125667822 12566782 Toxicity to various agents

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125667822 12566782 1 20160623 20160623 0
125667822 12566782 2 20160623 20160623 0
125667822 12566782 3 20160623 20160623 0