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
125873471 12587347 1 I 20160701 20160712 20160725 20160725 EXP GB-JNJFOC-20160709961 JOHNSON AND JOHNSON 41.00 YR A F Y 55.00000 KG 20160725 CN GB GB

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
125873471 12587347 1 PS PARACETAMOL ACETAMINOPHEN 1 Unknown Y Y 19872 TABLET
125873471 12587347 2 SS PARACETAMOL ACETAMINOPHEN 1 Unknown 500 (UNITS UNSPECIFIED) Y Y 19872 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125873471 12587347 2 Headache

Outcome of event

Event ID CASEID OUTC COD
125873471 12587347 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125873471 12587347 Nausea Nausea

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
125873471 12587347 2 20160630 20160702 0