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
126261941 12626194 1 I 20160730 20160731 20160805 20160805 EXP ES-ABBVIE-16K-144-1692940-00 ABBVIE 78.20 YR M Y 0.00000 20160805 CN COUNTRY NOT SPECIFIED ES

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
126261941 12626194 1 PS DUODOPA CARBIDOPALEVODOPA 1 Other UNKNOWN 203952
126261941 12626194 2 SS SINTROM ACENOCOUMAROL 1 Unknown Y UNKNOWN 0
126261941 12626194 3 C HEPARIN HEPARIN SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126261941 12626194 1 Parkinson's disease
126261941 12626194 2 Cardiac failure
126261941 12626194 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126261941 12626194 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126261941 12626194 Anaemia
126261941 12626194 Duodenal ulcer
126261941 12626194 Haematemesis
126261941 12626194 Haematochezia

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
126261941 12626194 1 20140113 0
126261941 12626194 2 201607 0
126261941 12626194 3 201607 0