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
126389341 12638934 1 I 20160801 20160809 20160809 EXP AU-BAUSCH-BL-2016-019112 BAUSCH AND LOMB 69.00 YR F Y 0.00000 20160809 OT AU AU

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
126389341 12638934 1 PS HYDROCORTISONE. HYDROCORTISONE 1 Unknown U 19116
126389341 12638934 2 SS MORPHINE MORPHINE 1 Unknown U 0
126389341 12638934 3 SS PRIVIGEN HUMAN IMMUNOGLOBULIN G 1 Unknown U 0
126389341 12638934 4 C ASPIRIN. ASPIRIN 1 0
126389341 12638934 5 C SERETIDE MDI NOS 2 0
126389341 12638934 6 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126389341 12638934 1 Product used for unknown indication
126389341 12638934 2 Product used for unknown indication
126389341 12638934 3 Product used for unknown indication
126389341 12638934 4 Product used for unknown indication
126389341 12638934 5 Product used for unknown indication
126389341 12638934 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126389341 12638934 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126389341 12638934 Back pain
126389341 12638934 Coma scale abnormal
126389341 12638934 Flank pain
126389341 12638934 Pallor
126389341 12638934 Unresponsive to stimuli

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

no results found

Therapies reported

no results found