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
121466375 12146637 5 F 20130221 20160725 20160304 20160802 EXP US-009507513-1603USA001849 MERCK 24.23 YR F Y 146.00000 KG 20160802 MD US US

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
121466375 12146637 1 PS IMPLANON ETONOGESTREL 1 Subdermal 68 MG/ONE IMPLANT EVERY THREE YEARS 233808001 21529 1 DF IMPLANT
121466375 12146637 2 SS IMPLANON ETONOGESTREL 1 Subdermal 1 DF, UNK 21529 1 DF IMPLANT

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121466375 12146637 1 Contraception

Outcome of event

Event ID CASEID OUTC COD
121466375 12146637 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
121466375 12146637 Complication associated with device
121466375 12146637 Device deployment issue
121466375 12146637 Device difficult to use
121466375 12146637 Incorrect drug administration duration
121466375 12146637 Migration of implanted drug
121466375 12146637 No adverse event

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
121466375 12146637 1 20130221 0
121466375 12146637 2 20130221 0