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
125875121 12587512 1 I 20160721 20160725 20160725 EXP CA-ROCHE-1800452 ROCHE 0.00 F Y 0.00000 20160725 CN CA CA

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
125875121 12587512 1 PS XENICAL ORLISTAT 1 Unknown U 20766 CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125875121 12587512 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125875121 12587512 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125875121 12587512 Lipid metabolism disorder
125875121 12587512 Uterine cancer
125875121 12587512 Weight loss poor

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
125875121 12587512 1 201509 0